User:Daniel Mietchen/Wikidata lists/Items with Disease Ontology IDs

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 * Related properties

class of disease
{| class='wikitable sortable' ! Article ! instance of ! subclass of ! description ! Disease Ontology ID ! MeSH tree code ! Commons category ! image
 * 1,4-phenylenediamine allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger 1,4-phenylenediamine
 * DOID:0040058
 * 1-chloro-2,4-dinitrobenzene allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger 1-chloro-2,4-dinitrobenzene
 * DOID:0040069
 * 17q11 microdeletion syndrome
 * class of disease
 * chromosomal deletion syndrome partial deletion of the long arm of chromosome 17
 * Human disease
 * DOID:0060403
 * 2,4-dinitrophenyl allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger 2,4-dinitrophenyl group
 * DOID:0040079
 * 2-hydroxyglutaric aciduria
 * class of disease
 * amino acid metabolic disorder neurometabolic disease cerebral organic aciduria rare genetic epilepsy amino acid or protein metabolism disease with epilepsy
 * amino acid metabolic disorder that is an autosomal recessive neurometabolic disorder characterized by the significant elevation of urinary levels of hydroxyglutaric acid causing progressive brain damage
 * DOID:0050573
 * 2q37 deletion syndrome
 * class of disease
 * chromosome abnormality intellectual disability chromosome 2q deletion chromosomal deletion syndrome
 * human disease
 * DOID:0111704
 * 3-methylcrotonyl-CoA carboxylase 1 deficiency
 * class of disease
 * 3-methylcrotonyl-CoA carboxylase deficiency
 * 3-methylcrotonyl-CoA carboxylase deficiency that has material basis in homozygous or compound heterozygous mutation in the gene encoding the alpha subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 3q27
 * DOID:0080579
 * 3-methylcrotonyl-CoA carboxylase 2 deficiency
 * class of disease
 * 3-methylcrotonyl-CoA carboxylase deficiency
 * human disease
 * DOID:0080580
 * 3-methylglutaconic aciduria 7A
 * class of disease
 * human disease
 * DOID:0081133
 * 3-methylglutaconic aciduria type 1
 * class of disease
 * 3-methylglutaconic aciduria genetic disease autosomal recessive disease
 * 3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22
 * DOID:0110002
 * 3-methylglutaconic aciduria type 4
 * class of disease
 * 3-methylglutaconic aciduria
 * 3-methylglutaconic aciduria that is characterized by mild or intermittent urinary excretion of 3-methylglutaconic acid
 * DOID:0110006
 * 3-methylglutaconic aciduria type IX
 * class of disease
 * 3-methylglutaconic aciduria genetic disease autosomal recessive disease
 * 3-methylglutaconic aciduria that has material basis in homozygous mutation in the TIMM50 gene on chromosome 19q13
 * DOID:0070002
 * 3MC syndrome 2
 * class of disease
 * 3MC syndrome
 * 3MC syndrome that has material basis in homozygous mutation in the COLEC11 gene on chromosome 2p25
 * DOID:0060576
 * 3MC syndrome 3
 * class of disease
 * 3MC syndrome
 * 3MC congenital syndrome associated with the COLEC10 gene on chromosome 8q24
 * DOID:0060577
 * 4-tert-butylphenol allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger 4-tert-butylphenol
 * DOID:0040068
 * 4-vinylcyclohexene dioxide respiratory allergy
 * class of disease
 * respiratory allergy
 * respiratory allergy that has allergic trigger 4-vinylcyclohexene dioxide
 * DOID:0040063
 * 46 XX gonadal dysgenesis
 * class of disease
 * gonadal dysgenesis
 * gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female
 * DOID:14450
 * C12.706.316.064.249 C12.706.316.309.193 C13.351.875.253.064.249 C13.351.875.253.309.193 C16.131.939.316.064.249 C16.131.939.316.309.193 C19.391.119.064.249 C19.391.119.309.193
 * 46,XX sex reversal 1
 * class of disease
 * XX male syndrome X-linked dominant disease
 * human disease
 * DOID:0111761
 * 46,XX sex reversal 2
 * class of disease
 * autosomal dominant disease XX male syndrome
 * human disease
 * DOID:0111763
 * 46,XX sex reversal 3
 * class of disease
 * XX male syndrome X-linked dominant disease
 * human disease
 * DOID:0111762
 * 46,XX sex reversal 4
 * class of disease
 * autosomal dominant disease XX male syndrome
 * human disease
 * DOID:0111764
 * 46,XY sex reversal 1
 * class of disease
 * Y-linked disease XY gonadal dysgenesis
 * human disease
 * DOID:0111778
 * 46,XY sex reversal 10
 * class of disease
 * hereditary lymphedema familial hypertrophic cardiomyopathy 46,XY partial gonadal dysgenesis XY gonadal dysgenesis autosomal dominant disease chromosomal deletion syndrome
 * human disease
 * DOID:0111775
 * 46,XY sex reversal 2
 * class of disease
 * XY gonadal dysgenesis X-linked disease
 * human disease
 * DOID:0111777
 * 46,XY sex reversal 3
 * class of disease
 * autosomal dominant disease XY gonadal dysgenesis
 * human disease
 * DOID:0111772
 * 46,XY sex reversal 4
 * class of disease
 * XY gonadal dysgenesis chromosomal deletion syndrome
 * human disease
 * DOID:0111771
 * 46,XY sex reversal 5
 * class of disease
 * XY gonadal dysgenesis autosomal recessive disease
 * human disease
 * DOID:0111776
 * 46,XY sex reversal 6
 * class of disease
 * XY gonadal dysgenesis autosomal dominant disease
 * human disease
 * DOID:0111769
 * 46,XY sex reversal 7
 * class of disease
 * autosomal recessive disease XY gonadal dysgenesis
 * human disease
 * DOID:0111774
 * 46,XY sex reversal 8
 * class of disease
 * autosomal recessive disease XY gonadal dysgenesis
 * human disease
 * DOID:0111773
 * 46,XY sex reversal 9
 * class of disease
 * autosomal dominant disease XY gonadal dysgenesis
 * human disease
 * DOID:0111770
 * ABCD syndrome
 * class of disease
 * autosomal recessive disease Waardenburg-Shah syndrome syndrome
 * Autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB)
 * DOID:0050600
 * ABri amyloidosis
 * class of disease
 * cerebral amyloid angiopathy ITM2B amyloidosis genetic disease autosomal dominant disease
 * human disease
 * DOID:0070029
 * ACTH-independent macronodular adrenal hyperplasia 1
 * class of disease
 * Cushing syndrome due to macronodular adrenal hyperplasia
 * human disease
 * DOID:0111623
 * ACTH-independent macronodular adrenal hyperplasia 2
 * class of disease
 * Cushing syndrome due to macronodular adrenal hyperplasia
 * human disease
 * DOID:0111624
 * AMED syndrome
 * class of disease
 * syndrome autosomal recessive disease digenic disease
 * human disease
 * DOID:0080952
 * APP-related cerebral amyloid angiopathy
 * class of disease
 * cerebral amyloid angiopathy autosomal dominant disease
 * A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3.
 * DOID:0070028
 * Aagenaes syndrome
 * class of disease
 * syndrome primary lymphedema with associated anomalies genetic vascular anomaly rare genetic hepatic disease syndromic lymphedema rare genetic immune disease disease
 * syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts
 * DOID:6691
 * Aagenaes syndrome
 * Primary intestinal lymphangiectasia (Waldmann's disease) - legs.jpg
 * Achard syndrome
 * class of disease
 * syndrome genetic disease
 * syndrome that involves arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet
 * DOID:6686
 * Achenbach syndrome
 * class of disease
 * skin disease
 * skin condition characterized by spontaneous focal hemorrhage into the palm or the volar surface of a finger
 * DOID:6687
 * Paroxysmal hand hematoma
 * Acinetobacter infectious disease
 * class of disease
 * gram-negative bacterial infection opportunistic bacterial infectious disease
 * Human disease
 * DOID:3091
 * C01.150.252.400.560.022
 * Adie syndrome
 * class of disease
 * syndrome abnormal pupillary function disease
 * neurological disorder characterized by a tonically dilated pupil
 * DOID:11549
 * C10.177.045 C10.292.562.700.250 C11.590.436.200 C11.710.800.180
 * Adie syndrome
 * Adies.png
 * African histoplasmosis
 * class of disease
 * histoplasmosis disease
 * Human disease
 * DOID:11315
 * African iron overload
 * class of disease
 * iron overload HFE hereditary haemochromatosis
 * hemochromatosis characterized by a predisposition to iron loading that is exacerbated by excessive intake of dietary iron, commonly related to consumption of tradition beer brewed in non-galvanized steel drums
 * DOID:0111033
 * African tick-bite fever
 * class of disease
 * spotted fever disease
 * spotted fever that has material basis in Rickettsia africae, which is transmitted by ticks
 * DOID:0050035
 * African tick bite fever
 * African tick bite fever - leg lesion.jpg
 * Alkhurma hemorrhagic fever
 * class of disease
 * Kyasanur forest disease
 * Human disease
 * DOID:0050308
 * Alkuraya-Kučinskas syndrome
 * class of disease
 * cerebral malformation autosomal recessive disease syndrome
 * human disease
 * DOID:0111555
 * Alpha-thalassemia mental retardation syndrome
 * class of disease rare disease developmental defect during embryogenesis designated intractable/rare disease
 * alpha thalassemia alpha-thalassemia-related diseases X-linked dominant disease X-linked intellectual disability ATR-X-related syndrome syndrome with 46,XY disorder of sex development syndrome with disorder of sex development of gynecological interest
 * alpha thalassemia that has material basis in mutation in the ATRX gene on Xq21
 * DOID:0110030
 * Alpha-thalassemia mental retardation syndrome
 * Atr-x.jpg
 * Alteración del estado mental
 * class of disease
 * schizophrenia disease
 * DOID:1229
 * F03.700.750.600
 * Alwadei syndrome
 * class of disease
 * autosomal recessive non-syndromic intellectual disability neurodevelopmental disorder
 * autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13
 * DOID:0080239
 * Alzheimer disease 10
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variation in the region 7q36
 * DOID:0110043
 * Alzheimer disease 11
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * An Alzheimer&#39;s disease that is characterized by an associated with variation in the region 9p22.1.
 * DOID:0110044
 * Alzheimer disease 12
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variation in the region 8p12-q22
 * DOID:0110045
 * Alzheimer disease 13
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variation in the region 1q21
 * DOID:0110046
 * Alzheimer disease 14
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variation in the region 1q25
 * DOID:0110047
 * Alzheimer disease 15
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variations in the region 3q22-q24
 * DOID:0110048
 * Alzheimer disease 16
 * class of disease
 * Alzheimer's disease
 * An Alzheimer&#39;s disease that is characterized by an associated with a risk allele in in the PCDH11X gene on chromosome Xq21.3.
 * DOID:0110036
 * Alzheimer disease 17
 * class of disease
 * Alzheimer's disease
 * Alzheimer&#39;s disease that is characterized by an associated with mutations in the gene TREM2
 * DOID:0110049
 * Alzheimer disease 18
 * class of disease
 * Alzheimer's disease
 * Alzheimer&#39;s disease that has material basis in a mutation in the ADAM10 gene on chromosome 15q21
 * DOID:0110050
 * Alzheimer disease 19
 * class of disease
 * Alzheimer's disease
 * Alzheimer&#39;s disease that is characterized by associated variants of the gene PLD3
 * DOID:0110051
 * Alzheimer disease 5
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease autosomal dominant disease
 * human disease
 * DOID:0110037
 * Alzheimer disease 6
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variation in the region 10q24
 * DOID:0110038
 * Alzheimer disease 7
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * Alzheimer&#39;s disease that is characterized by an associated with variation in the region 10p13
 * DOID:0110039
 * Alzheimer disease 8
 * class of disease
 * Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * An Alzheimer&#39;s disease that is characterized by an associated with variation in the region 20p12.2-q11.21.
 * DOID:0110041
 * Alzheimer's disease 1
 * class of disease
 * autosomal dominant disease Alzheimer's disease
 * Alzheimer&#39;s disease that has material basis in mutation in the gene encoding the amyloid precursor protein on chromosome 21q
 * DOID:0080348
 * Alzheimer's disease 9
 * class of disease
 * autosomal dominant disease Alzheimer's disease early-onset autosomal dominant Alzheimer disease
 * human disease
 * DOID:0111364
 * Ambras type hypertrichosis universalis congenita
 * class of disease
 * hypertrichosis hypertrichosis lanuginosa congenita
 * human disease
 * DOID:0111060
 * American histoplasmosis
 * class of disease
 * histoplasmosis
 * Human disease
 * DOID:1759
 * Angelucci's syndrome
 * class of disease
 * allergic conjunctivitis acute conjunctivitis
 * Human disease
 * DOID:11203
 * Arakawa's syndrome I
 * class of disease
 * syndrome disorder of folate metabolism and transport constitutional megaloblastic anemia due to folate metabolism disorder vitamin metabolic disorder autosomal recessive disease
 * genetic disorder
 * DOID:0111679
 * Arenaviridae infectious disease
 * class of disease
 * (-)ssRNA virus infectious disease viral infectious disease
 * human disease
 * DOID:3944
 * C02.782.082
 * Argyll Robertson pupil
 * class of disease
 * abnormal pupillary function disease
 * symptom of human disease
 * DOID:14523
 * Argyll Robertson pupil
 * Argyll Robertson pupil light reflex vs accommodation reflex.jpg
 * Askin's tumor
 * class of disease
 * Ewing sarcoma
 * Human disease
 * DOID:0050608
 * Astrakhan spotted fever
 * class of disease
 * spotted fever
 * Human disease
 * DOID:0050041
 * Atlantic cod allergy
 * class of disease
 * fish allergy
 * fish allergy triggered by Gadus morhua
 * DOID:0060514
 * Atlantic salmon allergy
 * class of disease
 * fish allergy
 * fish allergy triggered by Salmo salar
 * DOID:0060515
 * Axenfeld-Rieger syndrome
 * class of disease
 * autosomal dominant disease eye disease
 * autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment
 * DOID:14686
 * Axenfeld syndrome
 * Axenfeld-Rieger syndrome type 2
 * class of disease
 * Axenfeld-Rieger syndrome chromosomal deletion syndrome
 * Axenfeld-Rieger syndrome that has material basis in deletions in the region 13q14
 * DOID:0110121
 * B cell and dendritic cell deficiency
 * class of disease
 * combined immunodeficiency
 * human disease
 * DOID:0111964
 * B cell deficiency
 * class of disease
 * primary immunodeficiency disease
 * primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly
 * DOID:2115
 * B cell linker protein deficiency
 * class of disease
 * agammaglobulinemia autosomal recessive disease
 * Human disease
 * DOID:0060027
 * B-cell acute lymphoblastic leukemia
 * class of disease
 * acute lymphocytic leukemia lymphoma B-cell leukemia
 * human disease
 * DOID:0080638
 * B-cell adult acute lymphocytic leukemia
 * class of disease
 * adult acute lymphocytic leukemia B-cell childhood acute lymphoblastic leukemia lymphoma
 * Human disease
 * DOID:0060592
 * B-cell childhood acute lymphoblastic leukemia
 * class of disease
 * childhood acute lymphocytic leukemia B-cell acute lymphoblastic leukemia lymphoma
 * childhood acute lymphoblastic leukemia that has material basis in B-cells
 * DOID:0080146
 * B-cell lymphoma
 * class of disease
 * non-Hodgkin lymphoma leukocyte disease immune disorder
 * non-Hodgkin lymphoma that has material basis in B cells
 * DOID:707
 * C04.557.386.480.150 C15.604.515.569.480.150 C20.683.515.761.480.150
 * B-cell lymphomas
 * Lymphoma, B-cell type, small cell, well-differentaited Case 173 (5601360422).jpg
 * B-cell prolymphocytic leukemia
 * class of disease
 * prolymphocytic leukemia
 * human disease
 * DOID:0081041
 * B-lymphoblastic leukemia/lymphoma KMT2A rearranged
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080644
 * B-lymphoblastic leukemia/lymphoma with BCR-ABL1
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080643
 * B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080645
 * B-lymphoblastic leukemia/lymphoma with IL3-IGH
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080648
 * B-lymphoblastic leukemia/lymphoma with TCF3-PBX1
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080649
 * B-lymphoblastic leukemia/lymphoma with hyperdiploidy
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080646
 * B-lymphoblastic leukemia/lymphoma with hypodiploidy
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080647
 * B-lymphoblastic leukemia/lymphoma with iAMP21
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080651
 * B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like
 * class of disease
 * precursor B lymphoblastic lymphoma/leukemia
 * human disease
 * DOID:0080650
 * BIDS syndrome
 * class of disease
 * trichothiodystrophy syndromes autosomal recessive disease nonphotosensitive trichothiodystrophy
 * Human disease
 * DOID:0050528
 * Balkan hemorrhagic fever
 * class of disease
 * hemorrhagic fever with renal syndrome
 * Human disease
 * DOID:0050522
 * Balkan nephropathy
 * class of disease
 * interstitial nephritis Alport syndrome
 * interstitial nephritis endemic to the regions along the Danube river, in the modern countries of Croatia, Bosnia and Herzegovina, Serbia, Romania and Bulgaria
 * DOID:3052
 * C12.200.777.419.570.643.150 C12.050.351.968.419.570.643.150 C12.950.419.570.643.150
 * Balo concentric sclerosis
 * class of disease
 * demyelinating disease neurodegeneration multiple sclerosis disease
 * demyelinating disease characterized by the fact that the demyelinated tissues form concentric layers
 * DOID:0060215
 * Balo concentric sclerosis
 * Bardet-Biedl syndrome 1
 * class of disease
 * Bardet-Biedl syndrome
 * Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBS1 gene on chromosome 11q13
 * DOID:0110123
 * Barrett's adenocarcinoma
 * class of disease
 * esophagus adenocarcinoma
 * adenocarcinoma arising in Barrett&#39;s mucosa
 * DOID:7941
 * Barrett's esophagus
 * class of disease
 * esophageal disease disease
 * esophagus condition
 * DOID:9206
 * C04.834.154 C06.405.117.102
 * Barrett's esophagus
 * Barretts esophagus.jpg
 * Bartholin's duct cyst
 * class of disease
 * Bartholin's gland disease disease
 * cyst in a blocked Bartholin&#39;s gland
 * DOID:851
 * Bartholin's cyst
 * Barthonlincyst2011.png
 * Bartholin's gland adenocarcinoma
 * class of disease
 * Bartholin's gland carcinoma adenocarcinoma vulva adenocarcinoma
 * Human disease
 * DOID:6316
 * Bartholin's gland adenoid cystic carcinoma
 * class of disease
 * Bartholin's gland carcinoma Bartholin's gland adenocarcinoma
 * Human disease
 * DOID:4879
 * Bartholin's gland adenoma
 * class of disease
 * Bartholin's gland benign neoplasm benign epithelial neoplasm benign neoplasms by histologic type Bartholin's gland disease adenoma
 * Human disease
 * DOID:5382
 * Bartholin's gland adenomyoma
 * class of disease
 * Bartholin's gland benign neoplasm adenomyoma Bartholin's gland carcinoma Bartholin's gland disease
 * Human disease
 * DOID:6518
 * Bartholin's gland adenosquamous carcinoma
 * class of disease
 * adenosquamous carcinoma Bartholin's gland squamous cell carcinoma Bartholin's gland carcinoma
 * Bartholin&#39;s gland carcinoma that derives from squamous cells and gland-like cells
 * DOID:5630
 * Bartholin's gland benign neoplasm
 * class of disease
 * vestibular gland benign neoplasm bartholin gland neoplasm
 * Human disease
 * DOID:2068
 * Bartholin's gland cancer
 * class of disease
 * vulvar cancer Bartholin's gland disease
 * vulva cancer that is located in Bartholin&#39;s gland
 * DOID:60003
 * Bartholin's gland carcinoma
 * class of disease
 * vulva carcinoma Bartholin's gland benign neoplasm Bartholin's gland cancer disease
 * vulva carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in Bartholin&#39;s gland
 * DOID:3999
 * Bartholin's gland disease
 * class of disease
 * female reproductive system disease
 * Disease that is located in Bartholin&#39;s gland
 * DOID:60002
 * Bartholin's gland small cell carcinoma
 * class of disease
 * Bartholin's gland carcinoma female reproductive organ cancer small cell carcinoma
 * Human disease
 * DOID:7140
 * Bartholin's gland squamous cell carcinoma
 * class of disease
 * Bartholin's gland carcinoma squamous cell carcinoma vulva squamous cell carcinoma
 * Human disease
 * DOID:6961
 * Bartholin's gland transitional cell carcinoma
 * class of disease
 * Bartholin's gland carcinoma transitional cell carcinoma
 * Human disease
 * DOID:3998
 * Bartter disease type 1
 * class of disease
 * Bartter disease
 * A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21.
 * DOID:0110142
 * Bartter disease type 2
 * class of disease
 * Bartter disease
 * A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
 * DOID:0110143
 * Bartter disease type 4b
 * class of disease
 * Bartter disease infantile Bartter syndrome with sensorineural deafness
 * Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes
 * DOID:0110146
 * Bartter disease type 5
 * class of disease
 * Bartter disease
 * Bartter disease that has material basis in mutation in the MAGED2 gene on chromosome Xp11
 * DOID:0110147
 * Basilicata-Akhtar syndrome
 * class of disease
 * X-linked intellectual disability
 * human disease
 * DOID:0111838
 * Beckwith-Wiedemann syndrome
 * class of disease
 * syndrome overgrowth syndrome disease
 * syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations
 * DOID:5572
 * C16.131.077.133 C16.131.260.080 C16.320.180.080
 * Beemer-Langer syndrome
 * class of disease
 * short rib – polydactyly syndrome syndrome
 * syndrome that results in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly
 * DOID:9249
 * Behcet's syndrome arthropathy
 * class of disease
 * arthropathy Behçet's disease
 * Human disease
 * DOID:1670
 * Bell's palsy
 * class of disease symptom or sign
 * facial paralysis palsy disease
 * facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve)
 * DOID:12506
 * C01.925.256.466.087 C07.465.094 C07.465.299.250 C10.292.319.250
 * Bell's palsy
 * Bells palsy diagram.svg
 * Bellini duct carcinoma
 * class of disease
 * renal carcinoma renal cell carcinoma
 * disease
 * DOID:4464
 * Collecting duct carcinoma
 * Bernard-Soulier syndrome
 * class of disease
 * Giant platelet disorder inherited blood coagulation disease blood coagulation disease autosomal recessive disease disease
 * Human disease
 * DOID:2217
 * C15.378.100.100.080 C15.378.140.120 C15.378.463.080 C16.320.099.080
 * Blessig's cysts
 * class of disease
 * peripheral retinal degeneration retinoschisis and retinal cysts
 * Human disease
 * DOID:12164
 * Bordetella parapertussis whooping cough
 * class of disease
 * pertussis
 * A pertussis that is a milder disease caused by the bacterium Bordetella parapertussis. The disease has symptom coughing, has symptom sneezing, or has symptom runny nose.
 * DOID:11750
 * Borst-Jadassohn intraepidermal carcinoma
 * class of disease
 * skin carcinoma
 * Human disease
 * DOID:7039
 * Bowman's membrane folds or rupture
 * class of disease
 * corneal disease
 * Human disease
 * DOID:11552
 * Brainstem glioma
 * class of disease
 * brain stem cancer glioma brain glioma
 * Human disease
 * DOID:4202
 * Brainstem gliomas
 * Brown's tendon sheath syndrome
 * class of disease
 * mechanical strabismus genetic disease
 * Human disease
 * DOID:10235
 * Brown-Vialetto-Van Laere syndrome
 * class of disease
 * autosomal dominant disease infantile progressive bulbar palsy
 * Human disease
 * DOID:0050694
 * Brown-Vialetto-Van Laere syndrome 1
 * class of disease
 * autosomal recessive disease Brown-Vialetto-Van Laere syndrome
 * human disease
 * DOID:0080785
 * Brugada syndrome 1
 * class of disease
 * Brugada syndrome autosomal dominant disease
 * Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22
 * DOID:0110218
 * Brugada syndrome 7
 * class of disease
 * Brugada syndrome autosomal dominant disease
 * Brugada syndrome that has material basis in heterozygous mutation in the SCN3B gene on chromosome 11q24
 * DOID:0110224
 * Buruli ulcer disease
 * class of disease
 * primary bacterial infectious disease mycobacterium infectious disease neglected tropical disease disease
 * tropical disease
 * DOID:0050456
 * C01.150.252.410.040.552.475.247 C17.800.893.295
 * Buruli ulcer
 * Buruli ulcer left ankle EID.jpg
 * Buschke–Ollendorff syndrome
 * class of disease
 * osteopetrosis syndrome autosomal dominant disease
 * medical condition
 * DOID:0111536
 * Buschke–Ollendorff syndrome
 * C-P angle neurinoma
 * class of disease
 * neurilemmoma cerebellopontine angle tumor
 * Human disease
 * DOID:3199
 * CADASIL 1
 * class of disease
 * CADASIL autosomal dominant disease
 * CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13
 * DOID:0111035
 * CAKUT1
 * class of disease
 * CAKUT
 * human disease
 * DOID:0080206
 * CD3delta deficiency
 * class of disease
 * severe combined immunodeficiency T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta autosomal recessive disease primary immunodeficiency disease
 * A severe combined immunodeficiency that is characterized by the absence of T cells but normal numbers of B cells. CD3D is essential for T cell development.
 * DOID:0060016
 * CD3epsilon deficiency
 * class of disease
 * severe combined immunodeficiency autosomal recessive disease
 * Human disease
 * DOID:0060017
 * CD40 ligand deficiency
 * class of disease
 * combined immunodeficiency X-linked hyper IgM syndrome X-linked recessive disease
 * Human disease
 * DOID:0060022
 * CLOVES syndrome
 * class of disease
 * overgrowth syndrome subcutaneous tissue disease rare genetic vascular tumor nevus complex vascular malformation with associated anomalies genetic skin vascular disorder rare genetic subcutaneous tissue disorder syndrome PIK3CA-related overgrowth spectrum
 * CLOVE syndrome is characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, and Epidermal nevi
 * DOID:0080351
 * COACH Syndrome
 * class of disease
 * syndrome Joubert syndrome Joubert syndrome and related disorders autosomal recessive disease
 * a rare autosomal recessive disorder characterised by Cerebellar vermis hypoplasia, Oligophrenia (developmental delay/mental retardation), Ataxia, Coloboma, and Hepatic fibrosis.
 * DOID:0111589
 * CREST syndrome
 * class of disease
 * syndrome limited scleroderma disease
 * syndrome characterized by calcinosis, Raynaud&#39;s phenomeno, esophageal dysmotility, sclerodactyly and telangiectasia
 * DOID:0060218
 * C06.405.117.119.500.204 C14.907.617.812.500 C14.907.823.225 C17.300.799.801.500 C17.800.784.801.500 C18.452.174.130.204
 * CREST syndrome
 * Caplan's syndrome
 * class of disease
 * pneumoconiosis rheumatoid lung disease disease
 * pneumoconiosis that results in humans that also have rheumatoid arthritis
 * DOID:10326
 * C05.550.114.154.219 C05.799.114.219 C08.381.483.581.300 C08.381.520.702.300 C17.300.775.099.219 C24.800.340
 * Carrion's disease
 * class of disease
 * bartonellosis disease
 * infectious disease produced by Bartonella bacilliformis infection
 * DOID:0050398
 * Carrion's disease
 * Verruga peruana.jpg
 * Cervicocranial syndrome
 * class of disease
 * syndrome neurological disorder
 * syndrome that involves occipital head aches, nystagmus on head movement, tinnitus, spasms, blurred vision, corneal hyperaesthesia, and corneal ulcers
 * DOID:6692
 * C05.116.900.596
 * Chandler syndrome
 * class of disease
 * corneal dystrophy iridocorneal endothelial syndrome
 * Human disease
 * DOID:11554
 * Charcot-Marie-Tooth disease axonal type 2H
 * class of disease
 * Charcot-Marie-Tooth disease type 2 autosomal recessive axonal hereditary motor and sensory neuropathy autosomal recessive disease
 * Charcot-Marie-Tooth disease type 2 that has material basis in variation in the region 8q13-q23
 * DOID:0110166
 * Charcot-Marie-Tooth disease dominant intermediate A
 * class of disease
 * Charcot-Marie-Tooth disease intermediate type autosomal dominant intermediate Charcot-Marie-Tooth disease autosomal dominant disease
 * A Charcot-Marie-Tooth disease intermediate type that has material basis in variation in the region 10q24.1-q25.1.
 * DOID:0110202
 * Charcot-Marie-Tooth disease dominant intermediate G
 * class of disease
 * Charcot-Marie-Tooth disease intermediate type
 * human disease
 * DOID:0080294
 * Charcot-Marie-Tooth disease intermediate type
 * class of disease
 * Charcot–Marie–Tooth disease
 * Charcot-Marie-Tooth disease characterized by motor conduction velocities above and below 38 m/s
 * DOID:0050543
 * Charcot-Marie-Tooth disease type 1
 * class of disease
 * Charcot–Marie–Tooth disease autosomal dominant hereditary demyelinating motor and sensory neuropathy
 * Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons
 * DOID:0050538
 * Charcot-Marie-Tooth disease type 1G
 * class of disease
 * Charcot-Marie-Tooth disease type 1 autosomal dominant disease
 * human disease
 * DOID:0111560
 * Charcot-Marie-Tooth disease type 2A2B
 * class of disease
 * Charcot-Marie-Tooth disease type 2 autosomal recessive disease
 * human disease
 * DOID:0111557
 * Charcot-Marie-Tooth disease type 2DD
 * class of disease
 * autosomal dominant disease Charcot-Marie-Tooth disease type 2
 * human disease
 * DOID:0111558
 * Charcot-Marie-Tooth disease type 2EE
 * class of disease
 * Charcot-Marie-Tooth disease type 2 autosomal recessive disease
 * human disease
 * DOID:0111559
 * Charcot-Marie-Tooth disease type 3
 * class of disease
 * Charcot–Marie–Tooth disease
 * Human disease
 * DOID:0050540
 * Charcot-Marie-Tooth disease type 4
 * class of disease
 * Charcot–Marie–Tooth disease autosomal recessive hereditary demyelinating motor and sensory neuropathy
 * Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has material basis in autosomal recessive inheritance
 * DOID:0050541
 * Charcot-Marie-Tooth disease type 7
 * class of disease
 * Charcot–Marie–Tooth disease
 * Charcot-Marie-Tooth disease that is characterized by optic atrophy followed by retinitis pigmentosa
 * DOID:0080069
 * Charcot-Marie-tooth disease type 5
 * class of disease
 * Charcot–Marie–Tooth disease hereditary spastic paraplegia autosomal dominant disease
 * Charcot-Marie-Tooth disease that is characterized by pyramidal features including extensor plantar responses, mild increase in tone, and preserved or increased reflexes but no spastic gait
 * DOID:0080067
 * Chediak-Higashi syndrome
 * class of disease
 * autosomal recessive disease nervous system heredodegenerative disease eye degenerative disease syndrome disease
 * rare autosomal recessive disorder related to lysossomal function and the CHS1 gene
 * DOID:2935
 * C15.378.553.774.257 C20.673.774.257 C11.270.040.772
 * Chediak-Higashi syndrome
 * Clostridioides difficile colitis
 * class of disease
 * colitis Clostridium difficile intestinal infectious disease disease
 * colitis characterized by an overgrowth of Clostridioides difficile bacteria
 * DOID:0060185
 * C01.150.252.410.222.310 C06.405.205.596.800 C06.405.469.363.800
 * Pseudomembranous colitis
 * Clostridium difficile 01.jpg
 * Clostridium infectious disease
 * class of disease
 * bacterial infectious disease
 * Human disease
 * DOID:3584 DOID:0050351
 * C01.150.252.410.222
 * Coats disease
 * class of disease
 * retinal telangiectasia congenital vitreoretinal dysplasia secondary glaucoma due to a proliferation and differentiation anomaly genetic vascular disease genetic central nervous system and retinal vascular disease central nervous system and retinal vascular disease disease
 * Human disease
 * DOID:7765
 * C11.768.748 C14.907.823.502
 * Coats' disease
 * Eye of patient with Coats' disease.jpg
 * Coffin-Siris syndrome 1
 * class of disease
 * Coffin-Siris syndrome
 * An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ARID1B on chromosome 6q25.3.
 * DOID:0070042
 * Coffin-Siris syndrome 6
 * class of disease
 * Coffin-Siris syndrome
 * human disease
 * DOID:0080297
 * Cogan-Reese syndrome
 * class of disease
 * eye disease iridocorneal endothelial syndrome
 * eye disease characterized by variable iris atrophy, pigmented and pedunculated nodules located in iris and attachment of the iris to the cornea (peripheral anterior synechiae) and characterized by glaucoma
 * DOID:0060217
 * Conn's syndrome
 * class of disease
 * hyperaldosteronism adrenal adenoma adrenal gland disease disease
 * adrenal adenoma characterized by over production of aldosterone
 * DOID:12028
 * Primary aldosteronism
 * Aldosterone-2D-skeletal.svg
 * Cornelia de Lange syndrome 1
 * class of disease
 * Cornelia de Lange syndrome autosomal dominant disease
 * Cornelia de Lange syndrome that has material basis in heterozygous mutation in the NIPBL gene, which encodes a component of the cohesin complex, on chromosome 5p13
 * DOID:0080505
 * Cornelia de Lange syndrome 2
 * class of disease
 * Cornelia de Lange syndrome X-linked dominant disease
 * Cornelia de Lange syndrome that has material basis in a mutation in the SMC1A gene, which encodes a subunit of the cohesin complex, on chromosome Xp11
 * DOID:0080506
 * Cornelia de Lange syndrome 3
 * class of disease
 * Cornelia de Lange syndrome autosomal dominant disease
 * A Cornelia de Lange syndrome that has material basis in heterozygous mutation in the SMC3 gene on chromosome 10q25.2.
 * DOID:0080507
 * Cornelia de Lange syndrome 4
 * class of disease
 * Cornelia de Lange syndrome autosomal dominant disease
 * Cornelia de Lange syndrome that has material basis in heterozygous mutation in the RAD21 gene, which encodes a component of the cohesin complex, on chromosome 8q24
 * DOID:0080508
 * Cornelia de Lange syndrome 5
 * class of disease
 * Cornelia de Lange syndrome X-linked dominant disease
 * Cornelia de Lange syndrome that has material basis in by mutation in the HDAC8 gene on chromosome Xq13
 * DOID:0080509
 * Cortical blindness
 * class of disease
 * visual cortex disease cerebral visual impairment
 * human disease
 * DOID:11831
 * C10.597.751.941.162.250 C11.966.075.250 C23.888.592.763.941.162.250
 * Cowden syndrome 1
 * class of disease
 * autosomal dominant disease multiple hamartoma syndrome syndrome disease
 * inherited disorder causing tumor-like growth and increased cancer risk
 * DOID:6457
 * Cowden syndrome
 * Cowper gland carcinoma
 * class of disease
 * male reproductive organ cancer Littre gland carcinoma carcinoma
 * male reproductive organ cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the Cowper&#39;s gland
 * DOID:7632
 * Crohn's colitis
 * class of disease
 * Crohn's disease colitis
 * inflammatory bowel disease characterized by inflammation located in colon only
 * DOID:0060192
 * D-2-hydroxyglutaric aciduria 1
 * class of disease
 * D-2-hydroxyglutaric aciduria autosomal recessive disease
 * human disease
 * DOID:0111351
 * D-2-hydroxyglutaric aciduria 2
 * class of disease
 * autosomal dominant disease D-2-hydroxyglutaric aciduria
 * human disease
 * DOID:0111352
 * D-glycerate dehydrogenase deficiency
 * class of disease
 * primary hyperoxaluria
 * disease
 * DOID:0111671
 * D-glyceric aciduria
 * class of disease
 * inherited metabolic disorder autosomal recessive disease
 * human disease
 * DOID:0111626
 * D-mannitol allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger D-mannitol
 * DOID:0040019
 * DIC in newborn
 * class of disease
 * disseminated intravascular coagulation
 * Human disease
 * DOID:11246
 * De Barsy syndrome
 * class of disease
 * inborn disorder of ornithine or proline metabolism cutis laxa autosomal recessive disease
 * human disease
 * DOID:0070143
 * Diamond-Blackfan anemia 1
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111895
 * Diamond-Blackfan anemia 10
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111888
 * Diamond-Blackfan anemia 11
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111892
 * Diamond-Blackfan anemia 12
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111882
 * Diamond-Blackfan anemia 13
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111889
 * Diamond-Blackfan anemia 15 with mandibulofacial dysostosis
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111894
 * Diamond-Blackfan anemia 16
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111893
 * Diamond-Blackfan anemia 17
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111880
 * Diamond-Blackfan anemia 18
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111896
 * Diamond-Blackfan anemia 19
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111886
 * Diamond-Blackfan anemia 2
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111885
 * Diamond-Blackfan anemia 20
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111891
 * Diamond-Blackfan anemia 4
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111890
 * Diamond-Blackfan anemia 5
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111883
 * Diamond-Blackfan anemia 6
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111879
 * Diamond-Blackfan anemia 7
 * class of disease
 * autosomal dominant disease Diamond-Blackfan anemia
 * human disease
 * DOID:0111878
 * Diamond-Blackfan anemia 8
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111881
 * Diamond-Blackfan anemia 9
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111884
 * Diamond-blackfan anemia 3
 * class of disease
 * Diamond-Blackfan anemia autosomal dominant disease
 * human disease
 * DOID:0111887
 * Dieulafoy lesion
 * class of disease
 * stomach disease disease
 * Human disease
 * DOID:12070
 * Dieulafoy's lesion
 * Doyne honeycomb retinal dystrophy
 * class of disease
 * drusen genetic disease autosomal dominant disease
 * Human disease
 * DOID:0060745
 * Ehlers-Danlos syndrome arthrochalasia type 1
 * class of disease
 * Ehlers-Danlos syndrome autosomal dominant disease
 * human disease
 * DOID:0080727
 * Ehlers-Danlos syndrome arthrochalasia type 2
 * class of disease
 * autosomal dominant disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080728
 * Ehlers-Danlos syndrome cardiac valvular type
 * class of disease
 * Ehlers-Danlos syndrome autosomal recessive disease
 * human disease
 * DOID:0080730
 * Ehlers-Danlos syndrome classic type 2
 * class of disease
 * autosomal dominant disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080726
 * Ehlers-Danlos syndrome classic-like 1
 * class of disease
 * autosomal recessive disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080731
 * Ehlers-Danlos syndrome classic-like 2
 * class of disease
 * autosomal recessive disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080732
 * Ehlers-Danlos syndrome dermatosparaxis type
 * class of disease
 * autosomal recessive disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080733
 * Ehlers-Danlos syndrome kyphoscoliotic type 1
 * class of disease
 * Ehlers-Danlos syndrome autosomal recessive disease
 * human disease
 * DOID:0080734
 * Ehlers-Danlos syndrome kyphoscoliotic type 2
 * class of disease
 * autosomal recessive disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080735
 * Ehlers-Danlos syndrome musculocontractural type 1
 * class of disease
 * autosomal recessive disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080736
 * Ehlers-Danlos syndrome musculocontractural type 2
 * class of disease
 * Ehlers-Danlos syndrome autosomal recessive disease
 * human disease
 * DOID:0080737
 * Ehlers-Danlos syndrome spondylodysplastic type 1
 * class of disease
 * autosomal recessive disease Ehlers-Danlos syndrome Ehlers-Danlos syndrome progeroid type
 * human disease
 * DOID:0080738
 * Ehlers-Danlos syndrome spondylodysplastic type 3
 * class of disease
 * Ehlers-Danlos syndrome Ehlers-Danlos syndrome progeroid type
 * human disease
 * DOID:0080739
 * Ehlers-Danlos syndrome, periodontal type 2 Edspd2
 * class of disease
 * Ehlers-Danlos syndrome, periodontitis type Ehlers-Danlos syndrome autosomal dominant disease
 * human disease
 * DOID:0080987
 * Ehrlich tumor carcinoma
 * class of disease
 * breast carcinoma
 * Human disease
 * DOID:5050
 * C04.557.470.200.200 C04.619.169
 * Emery-Dreifuss muscular dystrophy 3, autosomal recessive
 * class of disease
 * Emery-Dreifuss muscular dystrophy autosomal recessive disease
 * human disease
 * DOID:0070248
 * Epstein-Barr virus hepatitis
 * class of disease
 * viral hepatitis
 * viral hepatitis that results in inflammation, located in liver, has material basis in Human herpesvirus 4 and has symptom headache, has symptom fatigue, has symptom fever, has symptom abdominal pain, has symptom nausea, and has symptom jaundice
 * DOID:0050204
 * Erdheim-Chester disease
 * class of disease
 * non-Langerhans-cell histiocytosis granulomatous autoinflammatory syndrome histiocytic and dendritic cell cancer connective tissue neoplasm immune disorder disease
 * rare disease
 * DOID:4329
 * C15.604.250.410.224
 * Erdheim–Chester disease
 * Maladie de Chester-Erdheim.png
 * Evans' syndrome
 * class of disease
 * primary thrombocytopenia autoimmune hemolytic anemia hemolytic anemia autoimmune thrombocytopenia
 * Human disease
 * DOID:8931
 * FTDALS3
 * class of disease
 * amyotrophic lateral sclerosis frontotemporal dementia behavioral variant of frontotemporal dementia FTDALS1 amyotrophic lateral sclerosis and frontotemporal dementia
 * amyotrophic lateral sclerosis that has material basis in mutation in the SQSTM1 gene on chromosome 5q35
 * DOID:0110068
 * Fanconi anemia complementation group A
 * class of disease
 * Fanconi anemia genetic disease autosomal recessive disease
 * Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24
 * DOID:0111095
 * Fanconi renotubular syndrome 1
 * class of disease
 * Fanconi syndrome autosomal dominant disease
 * human disease
 * DOID:0080757
 * Fanconi renotubular syndrome 2
 * class of disease
 * Fanconi syndrome autosomal recessive disease
 * human disease
 * DOID:0080758
 * Fanconi renotubular syndrome 3
 * class of disease
 * Fanconi syndrome autosomal dominant disease
 * human disease
 * DOID:0080759
 * Fanconi renotubular syndrome 4
 * class of disease
 * Fanconi syndrome autosomal dominant disease
 * human disease
 * DOID:0080760
 * Fanconi renotubular syndrome 5
 * class of disease
 * Fanconi syndrome autosomal recessive disease
 * human disease
 * DOID:0080761
 * Fanconi-like syndrome
 * class of disease
 * syndrome genetic disease
 * syndrome characterized by pancytopenia, immune deficiency and cutaneous malignancies
 * DOID:0090066
 * Far Eastern spotted fever
 * class of disease
 * spotted fever
 * Human disease
 * DOID:0050046
 * Foster-Kennedy syndrome
 * class of disease
 * papilledema disease
 * Human disease
 * DOID:14555
 * Fox-Fordyce disease
 * class of disease
 * sweat gland disease disease
 * chronic blockage of the sweat gland ducts with a secondary, non-bacterial inflammatory response to the secretions and cellular debris in the cysts
 * DOID:1381
 * C17.800.946.492.285
 * Fraser syndrome 1
 * class of disease
 * Fraser syndrome
 * human disease
 * DOID:0111405
 * Fraser syndrome 2
 * class of disease
 * Fraser syndrome
 * human disease
 * DOID:0111407
 * Fraser syndrome 3
 * class of disease
 * Fraser syndrome
 * human disease
 * DOID:0111406
 * French Canadian Leigh disease
 * class of disease
 * Leigh disease
 * human disease
 * DOID:0111180
 * Frey syndrome
 * class of disease
 * autonomic nervous system disease
 * human disease
 * DOID:11599
 * Frey's syndrome
 * Friedreich ataxia 1
 * class of disease
 * A Friedreich ataxia that has material basis in homozygous or compound heterozygous mutation in FXN on 9q21.1.
 * DOID:0111218
 * Friedreich ataxia 2
 * class of disease
 * Friedreich ataxia that has material basis in mutation in the 9p23-p11 chromosome region
 * DOID:0111219
 * Froelich syndrome
 * class of disease
 * hypothalamic disease
 * hypothalamic disease that is characterized by endocrine dysfunction of the hypothalamic gland resulting in delayed puberty, small testes, and obesity
 * DOID:6676
 * Adiposogenital dystrophy
 * Fuchs' endothelial dystrophy
 * class of disease
 * corneal endothelial dystrophy disease
 * corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet&#39;s membrane, leading to corneal edema and loss of vision
 * DOID:11555
 * C11.204.236.438 C11.270.162.438 C16.320.290.162.410
 * Fuchs' dystrophy
 * Fuchs' heterochromic uveitis
 * class of disease
 * uveitis syndrome
 * syndrome that is a chronic unilateral (or rarely bilateral) iridocyclitis appearing with the triad of heterochromia, predisposition to cataracts and glaucoma, and keratitic percipitates on the posterior corneal surface
 * DOID:9375
 * Fuchs heterochromic iridocyclitis
 * GM1 gangliosidosis type 1
 * class of disease
 * gangliosidosis GM1
 * GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis (see this term) with variable neurological and systemic manifestations
 * DOID:0080502
 * GM1 gangliosidosis type 2
 * class of disease
 * gangliosidosis GM1
 * GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age
 * DOID:0080501
 * GM2 gangliosidosis
 * class of disease
 * gangliosidosis nervous system heredodegenerative disease
 * human disease
 * DOID:3321
 * C10.228.140.163.100.435.825.300.300 C16.320.565.189.435.825.300.300 C16.320.565.398.641.803.350.300 C16.320.565.595.554.825.300.300 C18.452.132.100.435.825.300.300 C18.452.584.563.641.803.350.300 C18.452.648.189.435.825.300.300 C18.452.648.398.641.803.350.300 C18.452.648.595.554.825.300.300
 * GNE myopathy
 * class of disease
 * autosomal recessive disease muscular disease
 * human disease
 * DOID:0080718
 * GRID2-related autosomal dominant spinocerebellar ataxia
 * class of disease
 * spinocerebellar ataxia
 * human disease
 * DOID:0050988
 * GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
 * class of disease
 * frontotemporal lobar degeneration frontotemporal dementia primary progressive aphasia genetic disease autosomal dominant disease
 * Human disease
 * DOID:0060672
 * Galloway-Mowat syndrome 2
 * class of disease
 * Galloway-Mowat syndrome X-linked recessive disease
 * human disease
 * DOID:0080244
 * Galloway-Mowat syndrome 3
 * class of disease
 * Galloway-Mowat syndrome autosomal recessive disease
 * human disease
 * DOID:0080245
 * Galloway-Mowat syndrome 4
 * class of disease
 * Galloway-Mowat syndrome autosomal recessive disease
 * human disease
 * DOID:0080246
 * Galloway-Mowat syndrome 5
 * class of disease
 * Galloway-Mowat syndrome
 * human disease
 * DOID:0080247
 * Gasserian ganglion meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:7635
 * Gaucher's disease perinatal lethal
 * class of disease
 * Gaucher's disease genetic disease
 * Gaucher&#39;s Disease characterized by perinatal lethality and rapid progression of neurological deterioration that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22
 * DOID:0110960
 * Gaucher's disease type I
 * class of disease
 * Gaucher's disease genetic disease
 * Gaucher&#39;s disease characterized by absence of primary central nervous system involvement that has material basis in a mutation of GBA on chromosome 1q22
 * DOID:0110957
 * Gaucher's disease type II
 * class of disease
 * Gaucher's disease genetic disease
 * Gaucher&#39;s disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22
 * DOID:0110958
 * Gaucher's disease type III
 * class of disease
 * Gaucher's disease genetic disease
 * Gaucher&#39;s disease characterized by later onset and slower progession of neurological deterioration compared to type II that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22
 * DOID:0110959
 * Geleophysic dysplasia 2
 * class of disease
 * geleophysic dysplasia autosomal dominant disease
 * human disease
 * DOID:0111726
 * Gerstmann syndrome
 * class of disease
 * neurological disorder disease
 * nervous system disease that results from damage located in left parietal lobe, has symptom agraphia, has symptom acalculia, has symptom finger agnosia
 * DOID:4969
 * C10.597.606.762.100.300 C23.888.592.604.764.100.300
 * Gray728.svg
 * Gilbert syndrome
 * class of disease
 * bilirubin metabolic disorder disease
 * metabolic disorder in which the liver processes bilirubin slowly
 * DOID:2739
 * C16.320.565.300.528 C18.452.648.300.528
 * Bilirubin.svg
 * Glanzmann's thrombasthenia
 * class of disease
 * blood platelet disease inherited blood coagulation disease rare hemorrhagic disorder due to a qualitative platelet defect disease
 * human disease
 * DOID:2219
 * C15.378.100.100.820 C15.378.140.810 C15.378.463.810 C16.320.099.820
 * Good syndrome
 * class of disease
 * agammaglobulinemia combined immunodeficiency
 * agammaglobulinemia that is a condition where there is co-occurrence of deficient cell-mediated immunity and benign thymoma
 * DOID:0060028
 * Graves' disease
 * class of disease
 * autoimmune disease of endocrine system
 * autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located in thyroid gland
 * DOID:12361
 * C11.675.349.500 C19.874.283.605 C19.874.397.370 C20.111.555
 * Griscelli syndrome
 * class of disease
 * autosomal recessive disease integumentary system disease
 * autosomal recessive disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin
 * DOID:0060831
 * Griscelli syndrome type 2
 * class of disease
 * Griscelli syndrome
 * A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has material basis in mutation in the RAB27A gene on chromosome 15q21.3.
 * DOID:0060833
 * Griscelli syndrome type 3
 * class of disease
 * Griscelli syndrome
 * Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has material basis in mutation in the MLPH or MYO5A genes
 * DOID:0060834
 * Gulf War syndrome
 * class of disease
 * syndrome disease
 * illlnesses affecting Gulf War Vets
 * DOID:4491
 * C24.653
 * Pyridostigmine.svg
 * H syndrome
 * class of disease
 * histiocytosis autosomal recessive disease syndrome
 * genetic condition
 * DOID:0111278
 * HCL-V
 * class of disease
 * hairy cell leukemia
 * Human disease
 * DOID:713
 * HELLP syndrome
 * class of disease
 * severe pre-eclampsia disease
 * severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count
 * DOID:13133
 * C13.703.395.186
 * Haemodialysis-associated amyloidosis
 * class of disease
 * amyloidosis Dialytrauma ABeta2M amyloidosis acquired metabolic disease kidney disease
 * #946;2M) deposits in the musculoskeletal system leading to carpal tunnel syndrome (CTS), chronic arthropathy, cystic bone lesions, destructive osteoarthropathy, and pathologic fractures
 * DOID:0080928
 * Heart failure with preserved ejection fraction
 * class of disease
 * heart failure congestive heart failure
 * congestive heart failure wherein the amount of blood pumped from the heart&#39;s left ventricle with each beat (ejection fraction) is greater than 50%
 * DOID:9775
 * C14.280.434.611
 * Heimler syndrome 1
 * class of disease
 * deafness-enamel hypoplasia-nail defects syndrome peroxisomal biogenesis disorder autosomal recessive disease
 * human disease
 * DOID:0080623
 * Heimler syndrome 2
 * class of disease
 * deafness-enamel hypoplasia-nail defects syndrome peroxisomal biogenesis disorder autosomal recessive disease
 * human disease
 * DOID:0080624
 * Heinz body anemia
 * class of disease
 * congenital hemolytic anemia congenital nonspherocytic hemolytic anemia autosomal dominant disease
 * human disease
 * DOID:0111363
 * Henoch-Schoenlein purpura
 * class of disease
 * hypersensitivity vasculitis nonthrombocytopenic purpura disease
 * Human disease
 * DOID:11123
 * C14.907.940.777 C15.378.100.802.375 C15.378.463.515.580 C20.543.520.600 C23.550.414.950.375 C23.888.885.687.375
 * Henoch–Schönlein purpura
 * Henoch-schonlein-purpura.jpg
 * Her2-receptor negative breast cancer
 * class of disease
 * breast cancer
 * Human disease
 * DOID:0060080
 * Her2-receptor positive breast cancer
 * class of disease
 * breast cancer breast carcinoma by gene expression profile Hormone receptor positive breast tumor
 * Human disease
 * DOID:0060079
 * Hermansky-Pudlak syndrome 1
 * class of disease
 * Hermansky-Pudlak syndrome
 * A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS1 gene on chromosome 10q24.
 * DOID:0060539
 * Hermansky-Pudlak syndrome 2
 * class of disease
 * Hermansky-Pudlak syndrome
 * A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the gene encoding the beta-3A subunit of the AP3 complex (AP3B1) on chromosome 5q14.1.
 * DOID:0060540
 * Hermansky-Pudlak syndrome 3
 * class of disease
 * Hermansky-Pudlak syndrome
 * Hermasky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS3 gene on chromosome 3q24
 * DOID:0060541
 * Hermansky-Pudlak syndrome 4
 * class of disease
 * Hermansky-Pudlak syndrome
 * A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS4 gene on chromosome 22q12.1.
 * DOID:0060542
 * Hermansky-Pudlak syndrome 5
 * class of disease
 * Hermansky-Pudlak syndrome
 * Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the HPS5 gene on chromosome 11p14
 * DOID:0060543
 * Hermansky-Pudlak syndrome 6
 * class of disease
 * Hermansky-Pudlak syndrome
 * Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS6 gene on chromosome 10q24
 * DOID:0060544
 * Hermansky-Pudlak syndrome 7
 * class of disease
 * Hermansky-Pudlak syndrome
 * A Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the DTNBP1 gene on chromosome 6p22.3.
 * DOID:0060545
 * Hermansky-Pudlak syndrome 8
 * class of disease
 * Hermansky-Pudlak syndrome
 * Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the BLOC1S3 gene on chromosome 19q13
 * DOID:0060546
 * Hermansky-Pudlak syndrome 9
 * class of disease
 * Hermansky-Pudlak syndrome
 * human disease
 * DOID:0060547
 * Hirata disease
 * class of disease
 * autoimmune disease of endocrine system immune disorder hyperinsulinemic hypoglycemia
 * autoimmune disease of endocrine system characterized by hypoglycemia caused by antibodies to insulin
 * DOID:0040100
 * Hodgkin lymphoma
 * class of disease symptom or sign
 * lymphoma disease
 * lymphoma that is marked classically by the presence of Reed-Sternberg cells
 * DOID:8567
 * C04.557.386.355 C15.604.515.569.355 C20.683.515.761.355
 * Hodgkin's lymphoma
 * Hodgkin lymphoma (1) mixed cellulary type.jpg
 * Hodgkin's granuloma
 * class of disease
 * Hodgkin lymphoma
 * human disease
 * DOID:8651
 * Hodgkin's lymphoma, lymphocytic depletion
 * class of disease
 * Hodgkin lymphoma
 * Human disease
 * DOID:8628
 * Hodgkin's lymphoma, lymphocytic-histiocytic predominance
 * class of disease
 * Hodgkin lymphoma
 * Human disease
 * DOID:8543
 * Hodgkin's lymphoma, mixed cellularity
 * class of disease
 * Hodgkin lymphoma
 * human disease
 * DOID:8654
 * Hodgkin's lymphoma, nodular sclerosis
 * class of disease
 * Hodgkin lymphoma
 * Human disease
 * DOID:8838
 * Hodgkin's paragranuloma
 * class of disease
 * Hodgkin lymphoma
 * Human disease
 * DOID:8642
 * Horner's syndrome
 * class of disease
 * autonomic neuropathy disease
 * A disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)
 * DOID:11486
 * C10.177.350 C10.597.690.362.500 C11.710.528.500 C23.888.592.708.362.500
 * Horner's syndrome
 * Miosis.jpg
 * IDH-wildtype anaplastic astrocytoma
 * class of disease
 * anaplastic astrocytoma
 * human disease
 * DOID:0080876
 * IGSF1 deficiency syndrome
 * class of disease
 * central congenital hypothyroidism X-linked recessive disease syndrome
 * X-linked disease characterized by hypothyroidism that is present at birth, delayed testosterone increase in puberty, and testicular enlargement in adulthood that has material basis in mutation of the IGSF1 gene on chromosome Xq26
 * DOID:0111140
 * IgG4-related disease
 * class of disease
 * autoimmune connective tissue disorder autoimmune disease
 * systemic fibroinflammatory disease, associated with elevated serum IgG4 levels in about 60% of cases
 * DOID:0080356
 * C20.111.572
 * IgG4-related disease
 * Lesions of rectus muscles and nerves.jpg
 * Indian plum allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Ziziphus mauritiana plant fruit food product.
 * DOID:0060507
 * Indian prawn allergy
 * class of disease
 * shrimp allergy crustacean allergy
 * crustacean allergy triggered by Fenneropenaeus indicus
 * DOID:0060527
 * Indian tick typhus
 * class of disease
 * spotted fever
 * Human disease
 * DOID:0050042
 * Israeli tick typhus
 * class of disease
 * spotted fever
 * Human disease
 * DOID:0050043
 * Jaccoud's syndrome
 * class of disease
 * autoimmune disease joint disorder
 * Human disease
 * DOID:13080
 * Jaccoud arthropathy
 * Japanese spotted fever
 * class of disease
 * spotted fever
 * Human disease
 * DOID:0050050
 * Jewett-Marshall bladder cancer
 * class of disease
 * bladder carcinoma
 * Human disease
 * DOID:7315
 * Joubert syndrome 1
 * class of disease
 * Joubert syndrome
 * Joubert syndrome that has material basis in homozygous mutation in the INPP5E gene on chromosome 9q34
 * DOID:0110980
 * Joubert syndrome 10
 * class of disease
 * Joubert syndrome Joubert syndrome with orofaciodigital defect X-linked recessive disease
 * A Joubert syndrome that has material basis in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.
 * DOID:0110981
 * Joubert syndrome 13
 * class of disease
 * Joubert syndrome
 * Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TCTN1 gene on chromosome 12q24
 * DOID:0110982
 * Joubert syndrome 14
 * class of disease
 * Joubert syndrome Joubert syndrome with oculorenal defect Joubert syndrome with ocular defect
 * human disease
 * DOID:0110983
 * Joubert syndrome 15
 * class of disease
 * Joubert syndrome Joubert syndrome with ocular defect
 * Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has material basis in homozygous mutation in the CEP41 gene on chromosome 7q32
 * DOID:0110984
 * Joubert syndrome 17
 * class of disease
 * Joubert syndrome
 * Joubert syndrome characterized by episodic hyperpnea, abnormal eye movements, ataxia, and global psychomotor retardation that has material basis in compound heterozygous mutation in the C5ORF42 gene on chromosome 5p13
 * DOID:0110986
 * Joubert syndrome 18
 * class of disease
 * Joubert syndrome Joubert syndrome with orofaciodigital defect
 * Joubert syndrome that has material basis in homozygous mutation in the TCTN3 gene on chromosome 10q24
 * DOID:0110987
 * Joubert syndrome 20
 * class of disease
 * Joubert syndrome Joubert syndrome with ocular defect
 * Joubert syndrome that has material basis in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23
 * DOID:0110989
 * Joubert syndrome 21
 * class of disease
 * Joubert syndrome Joubert syndrome with Jeune asphyxiating thoracic dystrophy
 * Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CSPP1 gene on chromosome 8q13
 * DOID:0110990
 * Joubert syndrome 22
 * class of disease
 * Joubert syndrome Joubert syndrome with orofaciodigital defect
 * Joubert syndrome that has material basis in homozygous mutation in the PDE6D gene on chromosome 2q37
 * DOID:0110991
 * Joubert syndrome 23
 * class of disease
 * Joubert syndrome
 * human disease
 * DOID:0110992
 * Joubert syndrome 24
 * class of disease
 * Joubert syndrome
 * Joubert syndrome characterized by delayed psychomotor development and molar tooth sign on brain MRI that has material basis in homozygous mutation in the TCTN2 gene on chromosome 12q24
 * DOID:0110993
 * Joubert syndrome 25
 * class of disease
 * Joubert syndrome
 * human disease
 * DOID:0110994
 * Joubert syndrome 26
 * class of disease
 * Joubert syndrome
 * Joubert syndrome characterized by global developmental delay and cerebellar hypoplasia that has material basis in homozygous mutation in the KIAA0556 gene on chromosome 16p12
 * DOID:0110995
 * Joubert syndrome 27
 * class of disease
 * Joubert syndrome
 * Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the B9D1 gene on chromosome 17p11
 * DOID:0110996
 * Joubert syndrome 28
 * class of disease
 * Joubert syndrome Joubert syndrome with ocular defect
 * Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the MKS1 gene on chromosome 17q23
 * DOID:0110997
 * Joubert syndrome 29
 * class of disease
 * Joubert syndrome
 * human disease
 * DOID:0080276
 * Joubert syndrome 30
 * class of disease
 * Joubert syndrome
 * human disease
 * DOID:0080275
 * Joubert syndrome 31
 * class of disease
 * Joubert syndrome
 * human disease
 * DOID:0080277
 * Joubert syndrome 6
 * class of disease
 * Joubert syndrome
 * Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TMEM67 on chromosome 8q22
 * DOID:0111001
 * Joubert syndrome 7
 * class of disease
 * Joubert syndrome
 * A Joubert syndrome that has material basis in mutation in the RPGRIP1L gene on chromosome 16q12.2.
 * DOID:0111002
 * Joubert syndrome 8
 * class of disease
 * Joubert syndrome
 * A Joubert syndrome that has material basis in mutation in the ARL13B gene on chromosome 3q11.1-q11.2
 * DOID:0111003
 * Kallmann syndrome
 * class of disease
 * hypogonadotropic hypogonadism disease
 * A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects both males and females and causes a failure in puberty and infertility.
 * DOID:3614
 * C12.706.316.096.750 C13.351.875.253.096.750 C16.131.939.316.096.750 C16.320.467 C19.391.119.096.750 C19.391.482.600
 * Kallmann syndrome
 * Kanzaki disease
 * class of disease
 * Schindler disease
 * human disease
 * DOID:0112319
 * Kartagener syndrome
 * class of disease
 * primary ciliary dyskinesia situs inversus disease
 * primary ciliary dyskinesia that is characterized by sinusitis, bronchiectasis and situs inversus with dextrocardia resulting from dysfunction of the cilia during embryologic development
 * DOID:0050144
 * C08.127.384.500 C08.200.531 C08.695.501 C09.150.531 C14.240.400.280.500 C14.280.400.280.500 C16.131.077.245.500.531 C16.131.240.400.280.500 C16.131.740.501 C16.131.810.250.500 C16.320.184.500.531 C16.320.480
 * Kartagener syndrome
 * Kartagener.svg
 * Kawasaki disease
 * class of disease
 * lymphadenitis immune disorder predominantly medium-vessel vasculitis disease
 * human disease in which blood vessels throughout the body become inflamed
 * DOID:13378
 * C14.907.940.560 C15.604.560 C17.800.862.560
 * Kawasaki disease
 * Kawasaki Disease.png
 * Kelley–Seegmiller syndrome
 * class of disease
 * hypoxanthine-guanine phosphoribosyltransferase deficiency hyperuricemia X-linked recessive disease disease
 * human disease
 * DOID:0112127
 * Kimura disease
 * class of disease
 * skin disease
 * Human disease
 * DOID:7365
 * C07.465.815.178 C15.378.553.231.774 C15.604.315.459
 * King Denborough syndrome
 * class of disease
 * autosomal dominant disease
 * human disease
 * DOID:0080990
 * Klatskin's tumor
 * class of disease
 * intrahepatic cholangiocarcinoma disease
 * Human disease
 * DOID:4927 DOID:5246
 * C04.557.470.200.025.450.500
 * Kleefstra syndrome 1
 * class of disease
 * Kleefstra syndrome autosomal dominant disease chromosomal deletion syndrome
 * human disease
 * DOID:0060352
 * Kleefstra syndrome 2
 * class of disease
 * autosomal dominant disease Kleefstra syndrome
 * human disease
 * DOID:0080598
 * Klippel-Feil syndrome 1
 * class of disease
 * Klippel-Feil syndrome autosomal dominant disease
 * human disease
 * DOID:0080589
 * Klippel-Feil syndrome 2
 * class of disease
 * Klippel-Feil syndrome autosomal recessive disease
 * human disease
 * DOID:0080590
 * Klippel-Feil syndrome 3, autosomal dominant
 * class of disease
 * autosomal dominant disease Klippel-Feil syndrome
 * human disease
 * DOID:0080591
 * Klüver–Bucy syndrome
 * class of disease
 * impulse control disorder disease
 * syndrome resulting from bilateral lesions of the medial temporal lobe
 * DOID:2510
 * C10.228.140.380.326 F03.615.400.431
 * Kohler's disease
 * class of disease symptom or sign
 * osteochondrosis foot diseases disease
 * osteochondrosis that results in death and collapse located in navicular bone of foot
 * DOID:11760
 * Köhler disease
 * Köhler I.png
 * Korean hemorrhagic fever
 * class of disease
 * hemorrhagic fever with renal syndrome
 * Human disease
 * DOID:0050200
 * Kuhnt-Junius degeneration
 * class of disease
 * degeneration of macula and posterior pole
 * human disease
 * DOID:10873
 * C11.768.585.439.622
 * Kunjin encephalitis
 * class of disease
 * West Nile encephalitis
 * Human disease
 * DOID:0050174
 * Kuru
 * class of disease
 * transmissible spongiform encephalopathy disease
 * human disease
 * DOID:648
 * C10.228.228.800.435 C10.574.843.625 C01.207.800.435
 * Kuru (disease)
 * PMC4235695 pathogens-02-00472-g009.png
 * L-cell glucagon-like peptide producing tumor
 * class of disease
 * gastrointestinal neuroendocrine benign tumor
 * Human disease
 * DOID:7402
 * L1 syndrome
 * class of disease
 * X-linked intellectual disability hereditary spastic paraplegia X-linked complex spastic paraplegia nervous system heredodegenerative disease X-linked recessive disease
 * hereditary spastic paraplegia that is characterized by hydrocephalus, spasticity of the lower limbs, adducted thumbs, aphasia, seizures, agenesis of the corpus callosum and intellectual disability in the mild to moderate range
 * DOID:0060246 DOID:0110762
 * LEOPARD syndrome 1
 * class of disease
 * LEOPARD syndrome
 * LEOPARD syndrome that has material basis in heterozygous mutation in the PTPN11 gene on chromosome 12q24
 * DOID:0080548
 * LEOPARD syndrome 2
 * class of disease
 * LEOPARD syndrome
 * LEOPARD syndrome that has material basis in heterozygous mutation in the RAF1 gene on chromosome 3p25
 * DOID:0080549
 * LEOPARD syndrome 3
 * class of disease
 * LEOPARD syndrome
 * LEOPARD syndrome that has material basis in heterozygous mutation in the BRAF gene on chromosome 7q34
 * DOID:0080550
 * Lambert-Eaton myasthenic syndrome
 * class of disease
 * neuromuscular junction disease channelopathy immune-mediated acquired neuromuscular junction disease paraneoplastic neurologic syndrome autoimmune disease of musculoskeletal system autoimmune disease of peripheral nervous system disease
 * an autoimmune, presynaptic disorder of neuromuscular transmission characterized by fluctuating muscle weakness and autonomic dysfunction frequently associated with small-cell lung cancer (SCLC)
 * DOID:0050214
 * C04.588.614.550.500.225 C04.730.856.490.225 C10.114.656.150 C10.574.781.588.225 C10.668.758.725.150 C20.111.258.500.150
 * Synapse diag3.png
 * Langerhans cell sarcoma
 * class of disease
 * dendritic cell tumor leukocyte disease histiocytic and dendritic cell cancer sarcoma
 * histiocytic and dendritic cell cancer that derives from the lymph nodes, derives from the skin, derives from the liver, derives from the spleen and derives from bones
 * DOID:7146
 * C04.557.227.500 C15.604.250.390.500
 * Langerhans-cell histiocytosis
 * class of disease
 * histiocytosis disease
 * disease involving clonal proliferation of Langerhans cells
 * DOID:2571
 * C08.381.483.375 C15.604.250.400
 * Langerhans cell histiocytosis
 * Hans-Schuller-Christian.jpg
 * Leber congenital amaurosis 1
 * class of disease
 * Leber congenital amaurosis genetic disease autosomal recessive disease
 * Leber congenital amaurosis characterized by severe cone-rod dystrophy with photophobia, high hyperopia, and poor but stable vision with no visual improvement and that has material basis in mutation in the GUCY2D gene on chromosome 17p13
 * DOID:0110078
 * Leber hereditary optic neuropathy with demyelinating disease of CNS
 * class of disease
 * Leber plus disease
 * human disease
 * DOID:0111756
 * Leber optic atrophy and dystonia
 * class of disease
 * Leber plus disease
 * human disease
 * DOID:0111755
 * Leber plus disease
 * class of disease
 * Leber hereditary optic neuropathy syndrome
 * DOID:0111754
 * Lenz-Majewski hyperostotic dwarfism
 * class of disease
 * autosomal dominant disease syndrome osteochondrodysplasia
 * human disease
 * DOID:0111507
 * Lewy body dementia
 * class of disease
 * synucleinopathy dementia
 * type of dementia
 * DOID:12217
 * C10.228.140.079.862.400 C10.228.140.380.422 C10.228.662.600.200 C10.574.531 F03.615.400.512
 * Lewy body dementia
 * Lewy Koerperchen.JPG
 * Leydig cell tumor
 * class of disease
 * testicular sex cord-stromal neoplasm sex cord-gonadal stromal tumor
 * Human disease
 * DOID:2696
 * C04.557.475.750.847.249 C04.588.322.762.500.249 C04.588.945.440.915.500.249 C12.294.260.937.500.249 C12.758.409.937.500.249 C19.344.762.500.249 C19.391.829.782.500.249
 * Li-Fraumeni syndrome 1
 * class of disease
 * Li-Fraumeni syndrome
 * human disease
 * DOID:0111503
 * Li-Fraumeni syndrome 2
 * class of disease
 * Li-Fraumeni syndrome
 * human disease
 * DOID:0111504
 * Libman–Sacks endocarditis
 * class of disease
 * marantic endocarditis autoimmune disease of cardiovascular system endocarditis disease
 * human disease
 * DOID:0080740
 * Lisch epithelial corneal dystrophy
 * class of disease
 * epithelial and subepithelial dystrophy
 * Human disease
 * DOID:0060450
 * Littre gland carcinoma
 * class of disease
 * male reproductive organ cancer male urethral cancer carcinoma
 * male reproductive organ cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the Littre glands
 * DOID:6721
 * Livedoid vasculitis
 * class of disease
 * vasculitis
 * vasculitis with purpuric ulcers
 * DOID:0040099
 * C14.907.355.830.573 C17.800.862.406
 * Livedoid vasculitis
 * Loeffler endocarditis
 * class of disease
 * restrictive cardiomyopathy non-familial restrictive cardiomyopathy disease
 * restrictive cardiomyopathy that affects the endocardium and occurs with white blood cell proliferation, specifically of eosinophils
 * DOID:396
 * Loeffler syndrome
 * class of disease
 * eosinophilic pneumonia Acute eosinophilic pneumonia allergy disease
 * Human disease
 * DOID:9503
 * Loeys-Dietz syndrome 1
 * class of disease
 * Loeys-Dietz syndrome
 * Loeys-Dietz syndrome that has material basis in heterozygous mutation in the TGFBR1 gene on chromosome 9q22
 * DOID:0070235
 * Loeys-Dietz syndrome 2
 * class of disease
 * Loeys-Dietz syndrome
 * Loeys-Dietz syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p24
 * DOID:0070234
 * Loeys-Dietz syndrome 4
 * class of disease
 * Loeys-Dietz syndrome
 * human disease
 * DOID:0070233
 * Lown-Ganong-Levine syndrome
 * class of disease
 * syndrome pre-excitation syndrome genetic cardiac rhythm disease disease
 * syndrome that involves pre-excitation of the ventricles due to an accessory pathway providing an abnormal electrical communication from the atria to the ventricles
 * DOID:13087
 * C14.280.067.780.560
 * Lown-Ganong-Levine syndrome
 * Lynch syndrome
 * class of disease
 * autosomal dominant disease hereditary neoplastic syndromes colorectal cancer neoplasm syndrome disease
 * Human disease
 * DOID:3883
 * C04.588.274.476.411.307.190 C04.700.250 C06.301.371.411.307.190 C06.405.249.411.307.190 C06.405.469.158.356.190 C06.405.469.491.307.190 C16.320.700.250 C18.452.284.255
 * Lynch syndrome 1
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16
 * DOID:0070271
 * Lytico-bodig disease
 * class of disease
 * amyotrophic lateral sclerosis progressive supranuclear palsy neurodegenerative disease with dementia neurodegeneration
 * human disease
 * DOID:0111246
 * Léri–Weill dyschondrosteosis
 * class of disease
 * osteochondrodysplasia
 * human disease
 * DOID:0060847
 * MALT lymphoma
 * class of disease
 * marginal zone B-cell lymphoma primary cutaneous marginal zone lymphoma
 * non-Hodgkin lymphoma that has material basis in mucosal tissue involved in antibody production
 * DOID:0050909
 * C04.557.386.480.150.570 C15.604.515.569.480.150.570 C20.683.515.761.480.150.570
 * MHC class I deficiency
 * class of disease
 * severe combined immunodeficiency Bare lymphocyte syndrome
 * Human disease
 * DOID:0060009
 * MODY 1
 * class of disease
 * maturity-onset diabetes of the young
 * medical condition
 * DOID:0111099
 * MYH9-related disorder
 * class of disease
 * blood platelet disease Inherited giant platelet disorder
 * A blood platelet disease that has material basis in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.
 * DOID:0060651
 * Maffucci syndrome
 * class of disease
 * syndrome Ollier disease disease
 * syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple cavernous hemangiomas and phleboliths
 * DOID:0060221
 * Mahvash Disease
 * class of disease
 * endocrine pancreas disease autosomal recessive disease
 * human disease
 * DOID:0112306
 * Martinez Monasterio Pinheiro syndrome
 * class of disease
 * cleft lip and cleft palate hair diseases syndactyly
 * form of Blepharo-cheilo-dontic syndrome with with cleft lip and palate, complete absence of deciduous teeth, hypodontia of permanent teeth, hair alterations, hypertelorism, midface hypoplasia, abnormal EEG, syndactyly, and other findings
 * DOID:9003731
 * Masters-Allen syndrome
 * class of disease
 * female reproductive system disease
 * Human disease
 * DOID:14133
 * Mayer-Rokitansky-Kuster-Hauser syndrome
 * class of disease
 * syndrome
 * human disease
 * DOID:0112177
 * Mayer-Rokitansky-Kuster-Hauser syndrome type 1
 * class of disease
 * human disease
 * DOID:0112178
 * Meckel syndrome 1
 * class of disease
 * Meckel syndrome
 * Meckel syndrome that has material basis in an autosomal recessive mutation of MKS1 on chromosome 17q22
 * DOID:0070115
 * Meckel syndrome 13
 * class of disease
 * Meckel syndrome autosomal recessive disease
 * human disease
 * DOID:0080253
 * Meckel's diverticulitis
 * class of disease
 * diverticulitis
 * diverticulits characterized by the inflammation of a congenital diverticulum, which is a slight bulge of the small intestine present at birth
 * DOID:8408
 * Meckel's diverticulum
 * class of disease
 * genetic disease small intestine congenital defect diverticulum congenital disorder disease
 * congenital disorder of digestive system
 * DOID:9487
 * C06.198.859 C16.131.314.556 C23.300.415.750
 * Meckel's diverticulum
 * Diverticule de Meckel.jpg
 * Meckel's diverticulum cancer
 * class of disease
 * ileum cancer
 * Human disease
 * DOID:10152
 * Meesmann corneal dystrophy 1
 * class of disease
 * Meesmann corneal dystrophy autosomal dominant disease
 * human disease
 * DOID:0080670
 * Meesmann corneal dystrophy 2
 * class of disease
 * Meesmann corneal dystrophy autosomal dominant disease
 * human disease
 * DOID:0080671
 * Meier-Gorlin syndrome 1
 * class of disease
 * Meier-Gorlin syndrome autosomal recessive disease
 * Meier-Gorlin syndrome that has material basis in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32
 * DOID:0080512
 * Meige syndrome
 * class of disease
 * cranio-facial dystonia focal, segmental or multifocal dystonia
 * cranio-facial dystonia that is accompanied by blepharospasm
 * DOID:3982
 * C10.228.140.079.590 C10.228.662.300.500
 * Meige's syndrome
 * DeGaper.png
 * Merkel cell carcinoma
 * class of disease
 * skin carcinoma rare genetic developmental defect during embryogenesis genetic epidermal disorder skin tumor or hamartoma inherited neuroendocrine tumor genetic nervous system disorder malignant dermis tumor dermis disorder neuroendocrine tumor with other location nervous system cancer rare nervous system tumor disease
 * rare and highly aggressive skin cancer
 * DOID:3965
 * C02.256.721.150 C02.928.216 C04.557.465.625.650.240.325 C04.557.470.200.025.370.325 C04.557.580.625.650.240.325
 * Merkel cell carcinoma
 * Merkel cell cancer.jpg
 * Middle East respiratory syndrome
 * class of disease
 * acute viral respiratory tract infection coronavirus disease disease
 * viral respiratory infection in humans and camels
 * DOID:0080642
 * Middle East respiratory syndrome
 * MERS-CoV electron micrograph3.jpg
 * Milker's nodule
 * class of disease
 * viral infectious disease paravaccinia virus infection
 * Human disease
 * DOID:8729
 * Miller Fisher syndrome
 * class of disease symptom or sign
 * Guillain–Barré syndrome regional variant of Guillain-Barre syndrome
 * Guillain-Barre syndrome that manifests as a descending paralysis
 * DOID:12889
 * C10.114.750.100.500 C10.228.140.252.500 C10.292.562.350 C10.314.750.450.500 C10.668.829.350.500 C10.668.829.800.750.300.500 C11.590.312 C20.111.258.750.400.500
 * Miller–Dieker lissencephaly syndrome
 * class of disease symptom or sign
 * syndrome autosomal dominant classic lissencephaly autosomal dominant disease disease
 * A syndrome characterized by classical lissencephaly and distinct facial features. Visible and submicroscopic deletions of 17p13.3, including the LIS1 gene, are found in almost 100% of patients.
 * DOID:0060469
 * Mitis junctional epidermolysis bullosa
 * class of disease
 * junctional epidermolysis bullosa genetic disease autosomal recessive disease
 * human disease
 * DOID:0060738
 * Miyoshi muscular dystrophy
 * class of disease
 * distal muscular dystrophy
 * distal muscular dystrophy characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood
 * DOID:0070198
 * Miyoshi myopathy
 * Miyoshi muscular dystrophy 1
 * class of disease
 * Miyoshi muscular dystrophy genetic disease autosomal recessive disease
 * Miyoshi muscular dystrophy that has material basis in mutation in the DYSF gene on chromosome 2p13
 * DOID:0070199
 * Miyoshi muscular dystrophy 2
 * class of disease
 * Miyoshi muscular dystrophy
 * Miyoshi muscular dystrophy characterized by asymmetric presentation of muscle weakness and atrophy that has material basis in a locus on chromosome 10
 * DOID:0070200
 * Monckeberg arteriosclerosis
 * class of disease
 * arteriosclerosis vascular calcification
 * Human&#39;s arterial pathology
 * DOID:5161
 * C18.452.174.130.780.500
 * Monckeberg's arteriosclerosis
 * Mooren's ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10439
 * Morgagni cataract
 * class of disease
 * senile cataract
 * Human disease
 * DOID:13964
 * Mullegama-Klein-Martinez syndrome
 * class of disease
 * X-linked intellectual disability
 * human disease
 * DOID:0111845
 * Mycoplasma pneumonia
 * class of disease
 * atypical pneumonia bacterial pneumonia Mycoplasma pneumoniae infection
 * human disease
 * DOID:13276 DOID:0050154
 * C01.150.252.400.610.610.760 C01.150.252.620.500 C08.381.677.540.500 C08.730.610.540.545 C01.748.610.540.545
 * N,N'-diethylthiourea allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger N,N-diethylthiourea
 * DOID:0040102
 * N,N'-diphenylthiourea allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger N,N-diphenylthiourea
 * DOID:0040101
 * NK cell deficiency
 * class of disease
 * primary immunodeficiency disease
 * human disease
 * DOID:0080709
 * NUT midline carcinoma
 * class of disease
 * carcinoma rare tumor undifferentiated carcinoma
 * Human disease
 * DOID:0060463
 * NUT midline carcinoma
 * Nezelof syndrome
 * class of disease
 * thymic hypoplasia primary immunodeficiency disease autosomal recessive disease T cell deficiency
 * Human disease
 * DOID:2012
 * Niemann-Pick disease
 * class of disease
 * sphingolipidosis disease
 * severe metabolic disorders in which sphingomyelin accumulates in lysosomes in cells
 * DOID:14504
 * C10.228.140.163.100.435.825.700 C15.604.250.410.625 C16.320.565.189.435.825.700 C16.320.565.398.641.803.730 C16.320.565.595.554.825.700 C18.452.132.100.435.825.700 C18.452.584.687.803.730 C18.452.648.189.435.825.700 C18.452.648.398.641.803.730 C18.452.648.595.554.825.700
 * Niemann–Pick disease
 * Autorecessive-es.svg
 * Niemann-Pick disease type A
 * class of disease
 * Niemann-Pick disease genetic disease
 * A Niemann-Pick disease characterized by onset in infancy and involvement of neurological tissues that has material basis in an autosomal recessive mutation of SMPD1 on chromosome 11p15.4.
 * DOID:0070111
 * Niemann-Pick disease type B
 * class of disease
 * Niemann-Pick disease genetic disease
 * a Niemann-Pick disease characterized by visceral involvement only and survival into adulthood: material basis in an autosomal recessive mutation of SMPD1 on chromosome 11p15.4
 * DOID:0070112
 * C10.228.140.163.100.435.825.700.750 C15.604.250.410.625.750 C16.320.565.189.435.825.700.750 C16.320.565.398.641.803.730.750 C16.320.565.595.554.825.700.750 C18.452.132.100.435.825.700.750 C18.452.584.687.803.730.750 C18.452.648.189.435.825.700.750 C18.452.648.398.641.803.730.750 C18.452.648.595.554.825.700.750
 * Niemann-Pick disease, type C1
 * class of disease
 * Niemann-Pick disease Niemann–Pick disease, type C genetic disease
 * Type C Niemann-Pick disease associated with a mutation in the gene NPC1, encoding Niemann-Pick C1 protein
 * DOID:0070113
 * Niemann-Pick disease, type C2
 * class of disease
 * Niemann-Pick disease Niemann–Pick disease, type C genetic disease
 * A Niemann-Pick disease that has material basis in an autosomal recessive mutation of NPC2 on chromosome 14q24.3.
 * DOID:0070114
 * Nipah virus encephalitis
 * class of disease
 * viral encephalitis Nipah virus infection viral infectious disease
 * Human disease
 * DOID:0050192
 * Noonan syndrome 1
 * class of disease
 * Noonan syndrome
 * A Noonan syndrome disease type 1 that has material basis in the PTPN11 gene on chromosome 12q24.
 * DOID:0060578 DOID:0070101
 * Noonan syndrome 2
 * class of disease
 * Noonan syndrome autosomal recessive disease
 * Noonan syndrome that has material basis in an autosomal recessive mutation
 * DOID:0060580 DOID:0070102
 * Noonan syndrome-like disorder with loose anagen hair 1
 * class of disease
 * Noonan syndrome-like disorder with loose anagen hair
 * human disease
 * DOID:0080692
 * Noonan syndrome-like disorder with loose anagen hair 2
 * class of disease
 * Noonan syndrome-like disorder with loose anagen hair
 * human disease
 * DOID:0080693
 * Ollier disease
 * class of disease
 * syndrome enchondromatosis disease
 * rare nonhereditary sporadic disorder
 * DOID:4624
 * Ollier disease
 * Opitz GBBB syndrome type I
 * class of disease
 * X-linked recessive disease Opitz-GBBB syndrome
 * human disease
 * DOID:0080697
 * Opitz GBBB syndrome type II
 * class of disease
 * Opitz-GBBB syndrome
 * human disease
 * DOID:0080698
 * Oropouche fever
 * class of disease
 * viral infectious disease Bunyaviridae infectious disease disease
 * Human disease
 * DOID:0050521
 * Orthomyxoviridae infectious disease
 * class of disease
 * (-)ssRNA virus infectious disease
 * Human disease
 * DOID:4493
 * C01.925.782.620
 * Orthomyxoviridae infections
 * Osgood-Schlatter's disease
 * class of disease
 * bone inflammation disease knee disorder disease
 * osteochondrosis
 * DOID:7489
 * Osgood–Schlatter disease
 * Osgood.jpg
 * Pacinian tumor
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:2669
 * Paganini-Miozzo syndrome
 * class of disease
 * X-linked recessive disease X-linked intellectual disability
 * human disease
 * DOID:0111843
 * Pancoast tumor
 * class of disease
 * lung cancer pulmonary sulcus neoplasm disease
 * tumor of the pulmonary apex
 * DOID:8007
 * C04.588.894.797.520.734 C08.381.540.734 C08.785.520.734
 * Pancoast tumor
 * Pancoast Tumor 1.jpg
 * Parkinson's disease 21
 * class of disease
 * autosomal dominant disease hereditary late onset Parkinson disease
 * late onset Parkinson&#39;s disease characterized by autosomal dominant inheritance and mean age of onset at 67 years
 * DOID:0111251
 * Parkinson's disease 3
 * class of disease
 * Parkinson's disease
 * late onset Parkinson&#39;s disease characterized by mean age of onset of 59 years and that has material basis in mutation in a locus in the 2p13 chromosome region
 * DOID:0111250
 * Parry–Romberg syndrome
 * class of disease
 * facial nerve disease brain inflammatory disease inflammatory and autoimmune disease with epilepsy genetic peripheral neuropathy rare genetic epilepsy disease
 * a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body
 * DOID:1757
 * C07.465.284 C07.465.299.375 C10.292.319.375
 * Parry–Romberg syndrome
 * Parry Romberg Syndrome 1.jpg
 * Partington X-linked mental retardation syndrome
 * class of disease
 * X-linked intellectual disability X-linked recessive disease
 * syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria
 * DOID:14744
 * Patau syndrome
 * class of disease
 * chromosomal disease total autosomal trisomy trisomy 13 disease
 * Human disease
 * DOID:11665
 * C10.597.606.360.835 C14.240.400.970 C14.280.400.970 C16.131.240.400.965 C16.320.180.923 C16.131.260.923 C16.131.077.919
 * Patau syndrome
 * Chromosome 13.jpeg
 * Pearson syndrome
 * class of disease
 * mitochondrial disease
 * mitochondrial metabolism disease
 * DOID:0060067
 * Perrault syndrome 6
 * class of disease
 * Perrault syndrome
 * human disease
 * DOID:0080256
 * Peyronie's disease
 * class of disease
 * penile disease fibromatosis disease
 * Human disease
 * DOID:8616
 * C12.294.494.508 C17.300.715
 * Peyronie's disease
 * Peyronie disease.jpg
 * Phlegmonous dacryocystitis
 * class of disease
 * dacryocystitis
 * Human disease
 * DOID:12997
 * Plasmodium ovale malaria
 * class of disease
 * malaria
 * malaria characaterized as a relatively mild form caused by a parasite Plasmodium ovale, which is characterized by tertian chills and febrile paroxysms, and that ends spontaneously
 * DOID:12919
 * Pleomorphic xanthoastrocytoma
 * class of disease
 * astrocytoma low-grade astrocytoma
 * Human disease
 * DOID:4852
 * Pleomorphic xanthoastrocytoma
 * Plummer's disease
 * class of disease
 * hyperthyroidism nodular goiter
 * Human disease
 * DOID:11277
 * Posner-Schlossman Syndrome
 * class of disease
 * iridocyclitis
 * Human disease
 * DOID:9378
 * Potter's syndrome
 * class of disease
 * sequence renal agenesis disease
 * congenital disorder of urinary system
 * DOID:12594
 * Prieto syndrome
 * class of disease
 * X-linked intellectual disability X-linked recessive disease
 * Human disease
 * DOID:0060805
 * Prinzmetal's angina
 * class of disease
 * Vangina pectoris coronaropathy coronary artery vasospasm disease
 * cardiac chest pain at rest that occurs in cycles
 * DOID:0111151
 * C14.280.647.187.150.150 C14.907.585.187.150.500 C23.888.592.612.233.500.150.150
 * Pthirus pubis infestation
 * class of disease
 * ectoparasitism lice infestation
 * disease caused by the pubic louse, Pthirus pubis, a parasitic insect notorious for infesting human pubic hair
 * DOID:13760
 * Pubic lice
 * SOA-Pediculosis-pubis.jpg
 * Qazi Markouizos syndrome
 * class of disease
 * syndrome genetic syndromic intellectual disability
 * syndrome that is characterized by hypotonia, congenital fiber type disproportion and dysharmonic skeletal maturation
 * DOID:0050740
 * Quartan fever
 * class of disease
 * malaria
 * malaria caused by a parasite Plasmodium malariae, which is marked by recurrence of paroxysms at 72-hour intervals
 * DOID:14324
 * RASopathy
 * class of disease
 * genetic disease syndrome
 * Family of genetic conditions caused by mutations affecting Ras genes
 * DOID:0080690
 * REM sleep behavior disorder
 * class of disease
 * sleep disorder
 * sleep disorder that involves abnormal behavior including the acting out of violent or dramatic dreams during the sleep phase with rapid eye movement
 * DOID:9091
 * C10.886.659.633.700 F03.870.664.633.700
 * RNASET2-deficient cystic leukoencephalopathy
 * class of disease
 * autosomal recessive disease leukodystrophy
 * human disease
 * DOID:0081007
 * Raynaud disease
 * class of disease
 * peripheral vascular disease
 * Human disease
 * DOID:10300
 * C14.907.617.812
 * Raynaud's disease
 * Raynaud-Claes syndrome
 * class of disease
 * X-linked dominant disease X-linked intellectual disability
 * human disease
 * DOID:0112060
 * Reye syndrome
 * class of disease
 * syndrome encephalopathy systemic disease disease
 * syndrome characterized by acute brain damage and liver function problems
 * DOID:14525
 * C06.552.241.649 C10.228.140.163.780 C18.452.132.780
 * Reye's syndrome
 * Reye's syndrome liver-histology.jpg
 * Rh disease
 * class of disease
 * fetal erythroblastosis blood group incompatibility
 * problem with Rh+ fetuses in Rh- mothers
 * DOID:4175
 * G09.188.114.750 G12.122.780 G12.186.750
 * Richter's syndrome
 * class of disease
 * chronic lymphocytic leukemia disease
 * Human disease
 * DOID:1703
 * Rickettsia parkeri spotted fever
 * class of disease
 * spotted fever
 * A spotted fever that has material basis in Rickettsia parkeri, which is transmitted by Gulf Coast tick (Amblyomma maculatum). The infection has symptom fever, has symptom headache, has symptom eschar, and has symptom rash.
 * DOID:0050051
 * Riedel's fibrosing thyroiditis
 * class of disease
 * thyroiditis disease
 * thyroid disease
 * DOID:14351
 * Riley-Day syndrome
 * class of disease
 * hereditary sensory and autonomic neuropathy primary orthostatic hypotension rare genetic developmental defect during embryogenesis other dermis disorder other genetic dermis disorder nervous system anomaly with eye involvement autosomal recessive hereditary sensory and autonomic neuropathy disease
 * hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory
 * DOID:11589
 * C10.177.575.300 C10.500.310.309 C10.574.500.496.250 C10.668.829.800.175.250 C16.131.666.310.309 C16.320.400.415.309
 * Familial dysautonomia
 * Riley day.jpg
 * Ritscher-Schinzel syndrome 1
 * class of disease
 * Ritscher–Schinzel syndrome genetic disease
 * Ritscher-Schinzel syndrome that has material basis in homozygous mutation in the KIAA0196 gene on chromosome 8q24
 * DOID:0060571
 * Ritter's disease
 * class of disease
 * staphylococcal infection commensal bacterial infectious disease skin disease perinatal infectious disease disease
 * Human disease
 * DOID:9063
 * C01.150.252.410.868.951.770 C01.150.252.819.770.770 C01.800.720.770.770 C17.800.838.765.770.770
 * Staphylococcal scalded skin syndrome
 * OSC Microbio 21 02 SSSS.jpg
 * SAPHO syndrome
 * class of disease
 * syndrome autoinflammatory syndrome with skin involvement pyogenic autoinflammatory syndrome disease
 * variety of inflammatory bone disorders that may be associated with skin changes
 * DOID:13677
 * C05.116.099.708.025
 * Hiperostosis EC.JPG
 * SM-AHNMD
 * class of disease
 * systemic mastocytosis
 * Human disease
 * DOID:4797
 * SOST-related sclerosing bone dysplasia
 * class of disease
 * hyperostosis genetic disease autosomal recessive disease
 * hyperostosis that has material basis in a mutation in the SOST gene which results in overgrowth of endosteal bone producing dense and wide bones throughout the body especially located in skull
 * DOID:0080036
 * Sabinas brittle hair syndrome
 * class of disease
 * trichothiodystrophy syndromes genetic disease nonphotosensitive trichothiodystrophy
 * human disease
 * DOID:0111874
 * Sakati-Nyhan syndrome
 * class of disease
 * acrocephalosyndactylia
 * An acrocephalosyndactylia characterized by abnormalities in the bones of the legs, congenital heart defects and craniofacial defects and craniosynostosis. The patients suffer from cyanosis and other respiratory and breathing infections.
 * DOID:0060359
 * Sarcomatoid carcinoma of the lung
 * class of disease
 * large-cell lung carcinoma Sarcomatoid carcinoma lung carcinoma
 * medical condition
 * DOID:0080777
 * Sarcomatoid carcinoma of lung
 * Scheuermann's disease
 * class of disease
 * osteochondrosis kyphosis spinal osteochondrosis osteochondrosis of genetic origin spinal disease disease
 * osteochondrosis that results in abnormal bone growth and curvature located in thoracic vertebral column
 * DOID:13300
 * C05.116.821.500.500 C05.116.900.800.500.500 C05.116.900.808.500
 * Scheuermann's disease
 * Scheuermanns diseasebl.jpg
 * Schnitzler syndrome
 * class of disease
 * type IV hypersensitivity autoimmune urticaria unexplained periodic fever syndrome chronic urticaria
 * Human disease
 * DOID:4371
 * C20.683.780.640.700
 * Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma
 * class of disease
 * nodular ganglioneuroblastoma
 * Human disease
 * DOID:7951
 * Seckel syndrome 1
 * class of disease
 * Seckel syndrome
 * Seckel syndrome that has material basis in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23
 * DOID:0070007
 * Sertoli cell tumor
 * class of disease
 * testicular sex cord-stromal neoplasm sex cord-gonadal stromal tumor
 * Human disease
 * DOID:3577
 * C04.557.475.750.847.500 C04.588.322.762.500.500 C04.588.945.440.915.500.500 C12.294.260.937.500.500 C12.758.409.937.500.500 C19.344.762.500.500 C19.391.829.782.500.500
 * Sertoli cell tumor
 * Sertoli-Leydig cell tumor
 * class of disease
 * testicular sex cord-stromal neoplasm sex cord-gonadal stromal tumor
 * Human disease
 * DOID:2997
 * C04.557.475.750.847 C04.588.322.455.648 C04.588.322.762.500 C04.588.945.440.915.500 C12.294.260.937.500 C12.758.409.937.500 C13.351.500.056.630.705.648 C13.351.937.418.685.648 C19.344.410.648 C19.344.762.500 C19.391.630.705.648 C19.391.829.782.500
 * Sezary's disease
 * class of disease
 * cutaneous T cell lymphoma aggressive primary cutaneous T-cell lymphoma disease
 * type of cutaneous lymphoma
 * DOID:8541
 * C04.557.386.480.750.800.775 C15.604.515.569.480.750.800.775 C15.604.515.841 C20.683.515.761.480.750.800.775 C20.683.515.920
 * Sézary's disease
 * Sézary's disease.jpg
 * Sheehan's syndrome
 * class of disease
 * puerperal disorders necrosis of pituitary Simmonds' cachexia hypopituitarism disease
 * human disease
 * DOID:9476
 * Shukla-Vernon syndrome
 * class of disease
 * X-linked recessive disease syndrome
 * human disease
 * DOID:0111841
 * Shwartzman phenomenon
 * class of disease
 * vasculitis vascular hemostatic disease
 * Human disease
 * DOID:3825
 * C14.907.454.810 C14.907.940.890 C15.378.463.515.810
 * Simpson-Golabi-Behmel syndrome type 2
 * class of disease
 * X-linked recessive disease Simpson-Golabi-Behmel syndrome
 * X-linked recessive disease that has material basis in mutation in the OFD1 gene on chromosome Xp22 and is characterized by developmental delay, macrocephaly, and respiratory problems
 * DOID:0080342
 * Skene gland carcinoma
 * class of disease
 * paraurethral gland cancer carcinoma vulva adenocarcinoma
 * Human disease
 * DOID:7284
 * Smarca4-deficient sarcoma of thorax
 * class of disease
 * thoracic cancer
 * human disease
 * DOID:0080532
 * Sotos syndrome 1
 * class of disease
 * autosomal dominant disease Sotos syndrome
 * human disease
 * DOID:0112103
 * Sotos syndrome 2
 * class of disease
 * Sotos syndrome autosomal dominant disease
 * human disease
 * DOID:0112102
 * Spinal cord cancer
 * class of disease
 * central nervous system cancer spinal cord disease spinal cord neoplasm
 * central nervous system cancer that is located in the spinal cord
 * DOID:5612
 * Spirurida infectious disease
 * class of disease
 * filariasis
 * Human disease
 * DOID:1077
 * C01.610.335.508.700.750
 * Stickler syndrome 1
 * class of disease
 * Stickler syndrome autosomal dominant disease
 * human disease
 * DOID:0080676
 * Stickler syndrome type 2
 * class of disease
 * Stickler syndrome autosomal dominant disease
 * human disease
 * DOID:0080675
 * Sudeck's syndrome
 * class of disease
 * complex regional pain syndrome disease
 * Human disease
 * DOID:1811
 * C10.177.195.800 C10.668.829.250.800
 * Sugarman brachydactyly
 * class of disease
 * brachydactyly
 * brachydactyly characterized by a nonarticulating great toe set dorsal and proximal to the typical position
 * DOID:0110979
 * Sweeney-Cox syndrome
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0080538
 * T cell and NK cell immunodeficiency
 * class of disease
 * primary immunodeficiency disease
 * human disease
 * DOID:0080710
 * T cell deficiency
 * class of disease
 * primary immunodeficiency disease
 * Human disease
 * DOID:11200 DOID:613
 * Healthy Human T Cell.jpg
 * T cell, B cell, and NK cell deficiency
 * class of disease
 * combined immunodeficiency
 * human disease
 * DOID:0111965
 * T-cell acute lymphoblastic leukemia
 * class of disease
 * acute T cell leukemia lymphoma acute lymphocytic leukemia viral infectious disease T-cell leukemia
 * Acute lymphoblastic leukemia of T-cell origin. It comprises about 15% of childhood cases and 25% of adult cases. It is more common in males than females. (WHO, 2001)
 * DOID:5603 DOID:0050523
 * T-cell adult acute lymphocytic leukemia
 * class of disease
 * adult acute lymphocytic leukemia T-cell leukemia T-cell acute lymphoblastic leukemia
 * Human disease
 * DOID:5602
 * T-cell childhood acute lymphocytic leukemia
 * class of disease
 * childhood acute lymphocytic leukemia T-cell acute lymphoblastic leukemia
 * childhood acute lymphoblastic leukemia that has material basis in T-cells
 * DOID:0080145
 * T-cell childhood lymphoblastic lymphoma
 * class of disease
 * lymphoblastic lymphoma Precursor T-lymphoblastic lymphoma
 * lymphoblastic lymphoma that has material basis in T-cells and that occurs during childhood
 * DOID:0080148
 * T-cell large granular lymphocyte leukemia
 * class of disease
 * chronic lymphocytic leukemia acquired neutropenia T-cell leukemia disease
 * chronic lymphocytic leukemia that exhibits an unexplained, chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood
 * DOID:0050751
 * C04.557.337.428.580.049 C15.604.515.560.575.049 C20.683.515.528.582.049
 * T-cell leukemia
 * class of disease
 * leukocyte disease lymphoblastic leukemia disease
 * Human disease
 * DOID:715
 * C04.557.337.428.580 C15.604.515.560.575 C20.683.515.528.582
 * Taylor's syndrome
 * class of disease
 * uterine disease disease
 * Human disease
 * DOID:9346
 * Pelvic congestion syndrome
 * Teebi hypertelorism syndrome 2
 * class of disease
 * Hypertelorism, Teebi type
 * human disease
 * DOID:0081074
 * Timothy grass allergy
 * class of disease
 * pollen allergy
 * pollen allergy triggered by Phleum pratense pollen
 * DOID:0060498
 * Tn Polyagglutination syndrome
 * class of disease
 * genetic disease hematopoietic system disease
 * human disease
 * DOID:0080520
 * Treacher Collins syndrome 1
 * class of disease
 * Treacher Collins syndrome
 * human disease
 * DOID:0080789
 * Treacher Collins syndrome 2
 * class of disease
 * Treacher Collins syndrome autosomal recessive disease
 * human disease
 * DOID:0080790
 * Treacher Collins syndrome 3
 * class of disease
 * Treacher Collins syndrome autosomal recessive disease
 * human disease
 * DOID:0080791
 * Treacher Collins syndrome 4
 * class of disease
 * Treacher Collins syndrome
 * human disease
 * DOID:0080792
 * Trichohepatoenteric syndrome 2
 * class of disease
 * tricho-hepato-enteric syndrome
 * human disease
 * DOID:0111416
 * Turner syndrome
 * class of disease
 * gonadal dysgenesis X chromosome number anomaly with female phenotype disease
 * chromosomal disorder in which a female is partially or completely missing an X chromosome
 * DOID:3491
 * C12.050.351.875.253.309.872 C12.050.351.875.253.795.750 C12.200.706.316.309.872 C12.200.706.316.795.750 C14.240.400.980 C14.280.400.980 C16.131.240.400.970 C16.131.260.830.835.750 C16.131.939.316.309.872 C16.131.939.316.795.750 C16.320.180.830.835.750 C19.391.119.309.872 C19.391.119.795.750 C12.800.316.309.872 C12.800.316.795.750
 * Turner syndrome
 * 45,X.jpg
 * Uruguay faciocardiomusculoskeletal syndrome
 * class of disease
 * genetic disease syndrome cardiomyopathy
 * human disease
 * DOID:0112148
 * Usher syndrome type 1
 * class of disease
 * Usher syndrome
 * Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa
 * DOID:0110826
 * Usher syndrome type 1E
 * class of disease
 * Usher syndrome type 1
 * Usher syndrome type 1 that has material basis in variation in the chromosome region 21q21
 * DOID:0110833
 * Usher syndrome type 1H
 * class of disease
 * Usher syndrome type 1
 * human disease
 * DOID:0110835
 * Usher syndrome type 1K
 * class of disease
 * Usher syndrome type 1
 * An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.
 * DOID:0110837
 * Usher syndrome type 2
 * class of disease
 * Usher syndrome
 * Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa
 * DOID:0110827
 * Usher syndrome type 3
 * class of disease
 * Usher syndrome
 * Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life
 * DOID:0110828
 * VIPoma
 * class of disease
 * neuroendocrine tumor
 * rare endocrine tumor that overproduces vasoactive intestinal peptide
 * DOID:5574
 * C04.557.465.625.650.240.847 C04.557.470.200.025.370.847 C04.588.274.761.500.750 C04.588.322.475.500.750 C06.301.761.500.750 C06.689.667.500.750 C19.344.421.500.750
 * Van Esch-O'Driscoll syndrome
 * class of disease
 * X-linked recessive disease X-linked intellectual disability
 * human disease
 * DOID:0111840
 * Van Maldergem syndrome 1
 * class of disease
 * Van Maldergem syndrome
 * Van Maldergem syndrome that has material basis in homozygous mutation in the DCHS1 gene on chromosome 11p15
 * DOID:0080585
 * Van Maldergem syndrome 2
 * class of disease
 * Van Maldergem syndrome
 * Van Malergem syndrome that has material basis in homozygous or compound heterozygous mutation in the FAT4 gene on chromosome 4q28
 * DOID:0080586
 * Verruciform xanthoma
 * class of disease
 * xanthomatosis skin disease xanthoma
 * Human disease
 * DOID:5769
 * Volkmann's contracture
 * class of disease
 * connective tissue disease disease
 * permanent flexion contracture of the hand at the wrist, resulting in a claw-like deformity of the hand and fingers
 * DOID:5587
 * C05.550.323.734 C05.651.180.531 C05.651.197.734 C14.907.303.531
 * Volkmann's contracture
 * The practice of surgery (1910) (14756898256).jpg
 * WNT4 deficiency
 * class of disease
 * partial bilateral aplasia of the mullerian ducts sex differentiation disease autosomal dominant disease
 * human disease
 * DOID:0111526
 * Waardenburg syndrome type 1
 * class of disease
 * Waardenburg's syndrome
 * human disease
 * DOID:0110948
 * Waardenburg syndrome type 2B
 * class of disease
 * Waardenburg's syndrome
 * human disease
 * DOID:0110947
 * Waardenburg syndrome type 2C
 * class of disease
 * Waardenburg's syndrome
 * human disease
 * DOID:0110951
 * Waldenström macroglobulinemia
 * class of disease
 * B-cell lymphoma lymphoplasmacytic lymphoma disease
 * Type of blood cancer
 * DOID:0060901 DOID:0050747
 * C04.557.595.925 C14.907.454.960 C15.378.147.780.925 C15.378.463.515.960 C15.604.515.925 C20.683.780.925
 * Warburg micro syndrome 1
 * class of disease
 * Warburg micro syndrome
 * Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21
 * DOID:0110716
 * Waterhouse-Friderichsen syndrome
 * class of disease
 * adrenal crisis adrenal gland disease disease
 * adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland
 * DOID:9931
 * C01.150.252.223.500.750.500 C01.150.252.400.625.549.449.800 C10.228.228.180.500.750.500 C10.586.625.280.505.904 C15.378.100.802.843 C15.378.463.950 C19.053.500.740 C23.550.414.950.843 C23.888.885.687.843 C01.207.180.500.750.500
 * Waterhouse–Friderichsen syndrome
 * Waterhouse-Friderichsen. IMG 2912.jpg
 * Weissenbacher-Zweymuller syndrome
 * class of disease
 * Pierre Robin syndrome osteochondrodysplasia
 * human disease
 * DOID:4258
 * Wernicke encephalopathy
 * class of disease
 * encephalopathy long-term effects of alcohol consumption thiamine deficiency disease
 * presence of neurological symptoms caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves,
 * DOID:2384
 * C10.228.140.163.960 C18.452.132.960 C18.654.521.500.133.699.827.822 C25.775.100.625 F03.900.100.875
 * Whitewater Arroyo hemorrhagic fever
 * class of disease
 * viral infectious disease viral hemorrhagic fever
 * Human disease
 * DOID:0050199
 * Wolf-Hirschhorn syndrome
 * class of disease
 * chromosomal deletion syndrome partial deletion of the short arm of chromosome 4 disease
 * chromosome abnormality with a distinct craniofacial phenotype and intellectual disability
 * DOID:0050460
 * C16.131.077.944 C16.131.260.985 C16.320.180.985
 * Wolf–Hirschhorn syndrome
 * Mia - whs.jpg
 * Wolffian adnexal neoplasm
 * class of disease
 * uterine ligament cancer
 * Human disease
 * DOID:7514
 * Wolffian duct adenocarcinoma
 * class of disease
 * cervical adenocarcinoma mesonephric tumor clear cell adenocarcinoma
 * Human disease
 * DOID:5368
 * Wolffian duct adenoma
 * class of disease
 * reproductive organ benign neoplasm benign neoplasms by histologic type benign mesonephroma adenoma
 * Human disease
 * DOID:2616
 * Wolfram syndrome 1
 * class of disease
 * Wolfram syndrome autosomal recessive disease
 * Human disease
 * DOID:0110629
 * Wolfram syndrome 2
 * class of disease
 * Wolfram syndrome autosomal recessive disease
 * Human disease
 * DOID:0110630
 * Wolfram syndrome, mitochondrial form
 * class of disease
 * Wolfram syndrome
 * human disease
 * DOID:0080583
 * Wolman disease
 * class of disease
 * lysosomal and lipase deficiency
 * autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme
 * DOID:14497
 * C16.320.565.398.641.201.500 C16.320.565.595.201.500 C16.614.947 C18.452.584.563.641.201.500 C18.452.648.398.641.201.500 C18.452.648.595.201.500
 * Lysosomal acid lipase deficiency
 * X-Linked immunodeficiency 74
 * class of disease
 * X-linked recessive disease T cell deficiency
 * human disease
 * DOID:0112063
 * X-linked Emery-Dreifuss muscular dystrophy 1
 * class of disease
 * Emery-Dreifuss muscular dystrophy X-linked recessive disease
 * Emery-Dreifuss muscular dystrophy that has material basis in an X-linked recessive mutation of EMD on chromosome Xq28
 * DOID:0070246
 * X-linked Emery-Dreifuss muscular dystrophy 6
 * class of disease
 * Emery-Dreifuss muscular dystrophy X-linked recessive disease
 * An Emery-Dreifuss muscular dystrophy that has material basis in an X-linked recessive mutation of FHL1 on chromosome Xq26.3.
 * DOID:0070251
 * X-linked agammaglobulinemia type 2
 * class of disease
 * Bruton-type agammaglobulinemia autosomal recessive disease B cell deficiency
 * human disease
 * DOID:0111999
 * X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
 * class of disease
 * amelogenesis imperfecta
 * amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region
 * DOID:0110059
 * X-linked cardiac valvular dysplasia
 * class of disease
 * X-linked disease heart valve disease Heart valve dysplasia
 * human disease
 * DOID:0111765
 * X-linked chondrodysplasia punctata
 * class of disease
 * chondrodysplasia punctata X-linked recessive disease
 * Human disease
 * DOID:0060292
 * X-linked chondrodysplasia punctata 2
 * class of disease
 * X-linked dominant disease chondrodysplasia punctata
 * chondrodysplasia puncata that has material basis in mutation in the gene encoding delta(8)-delta(7) sterol isomerase emopamil-binding protein on chromosome Xp11
 * DOID:0080352
 * X-linked chronic granulomatous disease
 * class of disease
 * X-linked recessive disease chronic granulomatous disease
 * A chronic granulomatous disease characterized by X-linked inheritance that has material basis in mutation in the CYBB gene on chromosome Xp21.1-p11.4.
 * DOID:0070195
 * X-linked chronic idiopathic intestinal pseudo-obstruction
 * class of disease
 * X-linked recessive disease neuronal intestinal dysplasia
 * human disease
 * DOID:0080681
 * X-linked cone-rod dystrophy 2
 * class of disease
 * cone-rod dystrophy
 * cone-rod dystrophy that has material basis in variation in the chromosome region Xq27
 * DOID:0111006
 * X-linked congenital hemolytic anemia
 * class of disease
 * congenital hemolytic anemia X-linked recessive disease
 * human disease
 * DOID:0111846
 * X-linked congenital myopathy with fiber-type disproportion
 * class of disease
 * congenital fiber-type disproportion
 * A congenital fiber-type disproportion characterized by bilateral ptosis, facial weakness, impaired suckling, generalized hypotonia, and respiratory insufficiency that has material basis in mutation in the chromosome region Xq13.1-q22.1.
 * DOID:0111226
 * X-linked deafness 1
 * class of disease
 * X-linked nonsyndromic deafness
 * human disease
 * DOID:0111739
 * X-linked deafness 2
 * class of disease
 * X-linked nonsyndromic deafness
 * human disease
 * DOID:0111737
 * X-linked deafness 3
 * class of disease
 * X-linked nonsyndromic deafness
 * human disease
 * DOID:0111736
 * X-linked deafness 7
 * class of disease
 * X-linked nonsyndromic deafness
 * human disease
 * DOID:0111738
 * X-linked disease
 * class of disease
 * monogenic disease
 * monogenic disease that has material basis in mutations in genes on the X chromosome
 * DOID:0050735
 * C16.320.322
 * X-linked dyskeratosis congenita
 * class of disease
 * dyskeratosis congenita X-linked recessive disease
 * dyskeratosis congenita that has material basis in an X-linked recessive mutation of DKC1 on chromosome Xq28
 * DOID:0070025
 * X-linked endothelial corneal dystrophy
 * class of disease
 * corneal endothelial dystrophy posterior corneal dystrophy X-linked dominant disease
 * Human disease
 * DOID:0060446
 * X-linked exudative vitreoretinopathy 2
 * class of disease
 * X-linked disease exudative vitreoretinopathy
 * human disease
 * DOID:0111413
 * X-linked hyper IgM syndrome
 * class of disease
 * hyperimmunoglobulin syndrome hyper IgM syndrome X-linked recessive disease
 * human disease
 * DOID:6620
 * X-linked intellectual developmental disorder 108
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0111844
 * X-linked keratosis follicularis spinulosa decalvans
 * class of disease
 * keratosis follicularis spinulosa decalvans X-linked recessive disease
 * human disease
 * DOID:0080754
 * X-linked lymphoproliferative syndrome 2
 * class of disease
 * lymphoproliferative disorders X-linked lymphoproliferative disease X-linked recessive disease
 * Human disease
 * DOID:0060706
 * X-linked mental retardation 106
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0080240
 * X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques
 * class of disease
 * Olmsted syndrome X-linked recessive disease
 * human disease
 * DOID:0112012
 * X-linked nephrolithiasis type I
 * class of disease
 * renal tubular transport disease X-linked recessive disease
 * human disease
 * DOID:0111798
 * X-linked recessive hypoparathyroidism
 * class of disease
 * hypoparathyroidism, familial isolated hypoparathyroidism X-linked disease
 * human disease
 * DOID:0111388
 * X-linked retinitis pigmentosa and sinorespiratory infections
 * class of disease
 * syndrome X-linked disease
 * human disease
 * DOID:0112124
 * X-linked severe congenital neutropenia
 * class of disease
 * X-linked recessive disease severe congenital neutropenia
 * human disease
 * DOID:0112128
 * X-linked sideroblastic anemia
 * class of disease
 * Hereditary sideroblastic anemia X-linked recessive disease sideroblastic anaemia P
 * Human disease
 * DOID:0060063
 * X-linked spermatogenic failure 1
 * class of disease
 * Sertoli cell-only syndrome
 * Sertoli cell-only syndrome characterized by X-linked inheritance
 * DOID:0070189
 * X-linked spermatogenic failure 2
 * class of disease
 * azoospermia X-linked recessive disease
 * azoospermia characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has material basis in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13
 * DOID:0070185
 * X-linked spinal muscular atrophy 2
 * class of disease
 * X-linked recessive disease spinal muscular atrophy
 * human disease
 * DOID:0111827
 * X-linked spinocerebellar ataxia 1
 * class of disease
 * X-linked recessive disease X-linked cerebellar ataxia
 * human disease
 * DOID:0111829
 * X-linked spinocerebellar ataxia 2
 * class of disease
 * X-linked cerebellar ataxia
 * human disease
 * DOID:0111830
 * X-linked spinocerebellar ataxia 3
 * class of disease
 * X-linked cerebellar ataxia
 * human disease
 * DOID:0111831
 * X-linked spinocerebellar ataxia 5
 * class of disease
 * X-linked cerebellar ataxia X-linked recessive disease
 * human disease
 * DOID:0111833
 * XX male syndrome
 * class of disease syndrome anatomical abnormality
 * disorder of sex development X chromosome number anomaly with male phenotype gonadal dysgenesis disease
 * rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases
 * DOID:0111760
 * C12.050.351.875.253.064.124 C12.200.706.316.064.124 C12.800.316.064.124 C16.131.939.316.064.124 C19.391.119.064.124
 * Y-linked deafness
 * class of disease
 * nonsyndromic deafness Y-linked disease
 * human disease
 * DOID:0111757
 * Y-linked deafness 2
 * class of disease
 * Y-linked deafness
 * human disease
 * DOID:0111758
 * Y-linked disease
 * class of disease
 * monogenic disease Y linkage
 * monogenic disease that has material basis in muations on the Y chromosome
 * DOID:0050738
 * C16.320.338
 * Y-linked spermatogenic failure 1
 * class of disease
 * Sertoli cell-only syndrome Y-linked disease
 * Sertoli cell-only syndrome that has material basis in deletions in the Yq11 chromosomal region
 * DOID:0070186
 * Y-linked spermatogenic failure 2
 * class of disease
 * male infertility Y-linked disease spermatogenic failure
 * A male infertility characterized by nonobstroctive azoospermia or oligozoospermia that has material basis in interstitial deletions on the Yq11.221 chromosomal region.
 * DOID:0070187
 * Zenker's paralysis
 * class of disease
 * peripheral neuropathy common peroneal nerve lesion
 * medical condition
 * DOID:6925
 * Zollinger–Ellison syndrome
 * class of disease
 * syndrome disease
 * disease of the digestive tract in which tumors lead to excess acid and peptic ulcers
 * DOID:0050782
 * C04.730.713.988 C06.301.371.883 C06.405.249.883 C06.405.469.275.800.924 C06.405.469.965 C06.405.748.586.924 C06.405.748.947
 * Zollinger–Ellison syndrome
 * ZES endo.jpg
 * abacavir allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger abacavir
 * DOID:0040007
 * abdominal aortic aneurysm
 * class of disease
 * aortic aneurysm disease
 * aortic aneurysm that is located in the abdominal aorta
 * DOID:7693
 * C14.907.055.239.075 C14.907.109.139.075
 * Abdominal aortic aneurysm
 * AneurysmAortaWithArrows.jpg
 * abdominal obesity-metabolic syndrome
 * class of disease
 * autosomal dominant disease syndrome
 * Human disease
 * DOID:0060611
 * abdominal obesity-metabolic syndrome 3
 * class of disease
 * abdominal obesity-metabolic syndrome
 * abdominal obesity-metabolic syndrome that has material basis in heterozygous mutation in the DYRK1B gene on chromosome 19q13
 * DOID:0060612
 * abdominal tuberculosis
 * class of disease
 * extrapulmonary tuberculosis
 * extrapulmonary tuberculosis that is located in gastrointestinal tract, located in peritoneum, located in omentum, located in mesentery, located in liver, located in spleen or located in pancreas
 * DOID:0050599
 * Abdominal tuberculosis
 * abducens nerve neoplasm
 * class of disease
 * cranial nerve neoplasm abducens nerve palsy
 * Human disease
 * DOID:14125
 * abducens nerve palsy
 * class of disease
 * cranial nerve palsy paralytic squint
 * non-neoplastic or neoplastic disorder affecting the abducens nerve (sixth cranial nerve)
 * DOID:10865
 * C10.292.150
 * Sixth nerve palsy
 * abnormal pupillary function
 * class of disease
 * pupil disorder
 * Human disease
 * DOID:11518
 * abnormal retinal correspondence
 * class of disease
 * binocular vision disease
 * Human disease
 * DOID:12668
 * abnormal threshold of rods
 * class of disease
 * night blindness
 * Human disease
 * DOID:11874
 * abnormality of glucagon secretion
 * class of disease
 * endocrine pancreas disease
 * Human disease
 * DOID:14427
 * acalculous cholecystitis
 * class of disease
 * cholecystitis cystitis
 * Human disease
 * DOID:2828
 * C06.130.564.263.249
 * acanthocephaliasis
 * class of disease
 * parasitic helminthiasis infectious disease
 * Human disease
 * DOID:0050254
 * acantholytic acanthoma
 * class of disease
 * acanthoma
 * Human disease
 * DOID:4324
 * acantholytic squamous cell skin carcinoma
 * class of disease
 * cutaneous squamous-cell carcinoma keratinizing squamous cell carcinoma
 * Human disease
 * DOID:7643
 * acantholytic variant squamous cell breast carcinoma
 * class of disease
 * breast squamous cell carcinoma
 * Human disease
 * DOID:7459
 * acanthoma
 * class of disease
 * squamous cell neoplasm
 * Human disease
 * DOID:174
 * C04.557.470.700.040 C04.588.805.040
 * acanthosis nigricans
 * class of disease
 * pigmentation disorder disease
 * A skin condition characterised by dark, velvety patches in body folds and creases.
 * DOID:3138
 * C17.800.621.430.530.100
 * Acanthosis nigricans
 * Acanthosis-nigricans4.jpg
 * accessory nerve disease
 * class of disease
 * glossopharyngeal nerve disease
 * human disease
 * DOID:339
 * C10.292.175
 * Nervus accessorius
 * accommodative esotropia
 * class of disease
 * esotropia
 * Human disease
 * DOID:9839
 * accommodative spasm
 * class of disease
 * eye accommodation disease
 * Human disease
 * DOID:11637
 * achalasia
 * class of disease
 * esophageal disease disease
 * esophageal disease characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing
 * DOID:9164
 * C06.405.117.119.500.432
 * Achalasia
 * achilles bursitis
 * class of disease
 * bursitis foot diseases Achilles tendinitis
 * bursitis (inflammation of synovial sac) of bursa situated above the insertion of tendon to calcaneus
 * DOID:12857
 * achondrogenesis type IA
 * class of disease
 * achondrogenesis
 * achondrogenesis that results in abnormal ossification of the located in vertebral column or located in spine
 * DOID:0080054
 * achondrogenesis type IB
 * class of disease
 * achondrogenesis autosomal recessive disease
 * achondrogenesis that has material basis in mutation in the SLC26A2 gene which results in umbilical or inguinal hernia and a prominent rounded abdomen
 * DOID:0080055
 * achondrogenesis type II
 * class of disease
 * achondrogenesis autosomal dominant disease spinal disease
 * achondrogenesis that has material basis in mutations in the COL2A1 gene which results in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located in vertebral column or located in pelvis
 * DOID:0080056
 * achromatopsia 2
 * class of disease
 * achromatopsia autosomal recessive disease
 * An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
 * DOID:0110007
 * achromatopsia 3
 * class of disease
 * achromatopsia autosomal recessive disease
 * An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.
 * DOID:0110008
 * achromatopsia 4
 * class of disease
 * achromatopsia
 * achromatopsia that has material basis in homozygous or compound heterozygous mutation in the GNAT2 gene (139340) on chromosome 1p13
 * DOID:0110010
 * achromatopsia 7
 * class of disease
 * achromatopsia autosomal recessive disease
 * An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23.
 * DOID:0110009
 * acid anhydride respiratory allergy
 * class of disease
 * respiratory allergy
 * respiratory allergy that has allergic trigger acid anhydride
 * DOID:0040081
 * acinar cell carcinoma
 * class of disease
 * carcinoma
 * carcinoma that has material basis in abnormally proliferating cells, derives from spindle cells and/or derives from giant cells
 * DOID:3025
 * C04.557.470.200.025.215
 * acinar cell cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma cystadenocarcinoma
 * Human disease
 * DOID:7729
 * acinic cell breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive ductal carcinoma acinar cell carcinoma
 * Human disease
 * DOID:5743
 * acquired angioedema
 * class of disease
 * angioedema
 * human disease
 * DOID:0080941
 * acquired color blindness
 * class of disease
 * color blindness
 * human disease
 * DOID:13912
 * acquired gastric outlet stenosis
 * class of disease
 * pyloric stenosis
 * Human disease
 * DOID:14099
 * acquired generalized lipodystrophy
 * class of disease
 * lipodystrophy complete generalized lipodystrophy rare skin disease insulin resistance acquired lipodystrophy
 * complete generalized lipodystrophy that is charcterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth
 * DOID:0080300
 * acquired hemangioma
 * class of disease
 * hemangioma
 * Human disease
 * DOID:492
 * acquired hyperkeratosis
 * class of disease
 * keratosis
 * Human disease
 * DOID:13072
 * acquired metabolic disease
 * class of disease
 * metabolic disease
 * human disease
 * DOID:0060158
 * acquired night blindness
 * class of disease
 * nutritional deficiency disease night blindness
 * Human disease
 * DOID:11491
 * acquired polycythemia
 * class of disease
 * polycythemia
 * Human disease
 * DOID:2834
 * acquired tear duct stenosis
 * class of disease
 * lacrimal apparatus disease
 * Human disease
 * DOID:13655
 * acquired thrombocytopenia
 * class of disease
 * thrombocytopenia
 * Human disease
 * DOID:11126
 * acquired von Willebrand syndrome
 * class of disease
 * blood coagulation disease von Willebrand's disease rare hemorrhagic disorder due to an acquired coagulation factor defect
 * human disease
 * DOID:0111146
 * acral lentiginous melanoma
 * class of disease
 * skin melanoma disease
 * kind of lentiginous skin melanoma
 * DOID:6367
 * Skin Tumors-010.jpg
 * acrocephalosyndactylia
 * class of disease
 * synostosis craniosynostosis syndactyly disease
 * group of diseases
 * DOID:12960
 * C05.116.099.370.894.232.015 C05.116.099.370.894.819.100 C05.660.207.240.100 C05.660.585.800.100 C05.660.906.364.100 C05.660.906.819.100 C16.131.621.207.240.100 C16.131.621.585.800.100 C16.131.621.906.364.100 C16.131.621.906.819.100
 * Acrocephalosyndactyly
 * acrodermatitis
 * class of disease
 * dermatitis Foot Dermatoses
 * dermatitis that selectively affects the hands and feet
 * DOID:2722
 * C16.131.831.066 C17.800.174.100 C17.800.804.066
 * Acrodermatitis
 * acrodermatitis chronica atrophicans
 * class of disease
 * acrodermatitis Lyme disease
 * An acrodermatitis characterized by a chronically progressive course, leading to widespread atrophy of the skin. It is a clinical manifestation of Lyme borreliosis.
 * DOID:0060344
 * acrofacial dysostosis
 * class of disease
 * dysostosis
 * human disease
 * DOID:0060379
 * acropustulosis
 * class of disease
 * dermatitis acrodermatitis pustulosis genodermatosis other epidermal disorder genetic epidermal disorder
 * Human disease
 * DOID:4398
 * Acropustulosis
 * acrorenal syndrome
 * class of disease
 * syndrome autosomal recessive disease
 * Human disease
 * DOID:0060347
 * actinic keratosis
 * class of disease
 * pre-malignant neoplasm dermatoheliosis disease
 * human disease
 * DOID:8866
 * C04.834.450 C17.800.428.570
 * Actinic keratosis
 * Actinic keratosis on the lip.JPEG
 * activated PI3K delta syndrome
 * class of disease
 * agammaglobulinemia combined immunodeficiency autosomal dominant disease
 * medical condition
 * DOID:0111936
 * Autosomal dominant - en.svg
 * active cochlear Meniere's disease
 * class of disease
 * Meniere's disease
 * Human disease
 * DOID:13492
 * active cochleovestibular Meniere's disease
 * class of disease
 * Meniere's disease
 * Human disease
 * DOID:13490
 * active peptic ulcer disease
 * class of disease
 * peptic ulcer disease stomach bleeding
 * Human disease
 * DOID:749
 * C06.405.227.700 C23.550.414.788.700
 * active vestibular Meniere's disease
 * class of disease
 * Meniere's disease
 * Human disease
 * DOID:13491
 * acute T cell leukemia
 * class of disease
 * T-cell leukemia
 * Human disease
 * DOID:5603
 * acute allergic serous otitis media
 * class of disease
 * acute serous otitis media allergy
 * acute serous otitis media caused by an allergen
 * DOID:11558
 * acute apical periodontitis
 * class of disease
 * periapical periodontitis
 * Human disease
 * DOID:11693
 * acute asthma
 * class of disease
 * asthma
 * human disease
 * DOID:0080810
 * acute basophilic leukemia
 * class of disease
 * acute myeloid leukemia bilineal acute myeloid leukemia
 * rare acute myeloid leukemia in which the immature cells differentiate towards basophils
 * DOID:0080795
 * C04.557.337.539.275.125
 * acute biphenotypic leukaemia
 * class of disease
 * mixed phenotype acute leukemia acute lymphocytic leukemia acute leukemia lymphoma disease
 * uncommon type of leukemia which arises in multipotent progenitor cells which have the ability differentiating into both myeloid and lymphoid lineages
 * DOID:9953
 * C04.557.337.428.100 C15.604.515.560.100 C20.683.515.528.100
 * acute canaliculitis
 * class of disease
 * acute inflammation of lacrimal passage canaliculitis
 * Human disease
 * DOID:6969
 * acute cervicitis
 * class of disease
 * cervicitis acute disease
 * human disease
 * DOID:10616
 * acute chest syndrome
 * class of disease
 * lung disease
 * human disease
 * DOID:1584
 * C08.381.074 C08.618.009 C15.378.071.141.150.150.219 C15.378.420.155.219 C16.320.070.150.219 C16.320.365.155.219
 * acute cholangitis
 * class of disease
 * ascending cholangitis
 * Human disease
 * DOID:14271
 * acute closed-angle glaucoma
 * class of disease
 * primary angle-closure glaucoma
 * glaucoma
 * DOID:13862
 * Acute Angle Closure-glaucoma.jpg
 * acute conjunctivitis
 * class of disease
 * conjunctivitis
 * Human disease
 * DOID:11184
 * acute contagious conjunctivitis
 * class of disease
 * acute conjunctivitis
 * Human disease
 * DOID:11213
 * acute cor pulmonale
 * class of disease
 * acute pulmonary heart disease
 * Human disease
 * DOID:8517
 * acute dacryoadenitis
 * class of disease
 * dacryoadenitis
 * Human disease
 * DOID:952
 * acute dacryocystitis
 * class of disease
 * dacryocystitis
 * Human disease
 * DOID:12996
 * acute diarrhea
 * class of disease symptom or sign
 * diarrhea
 * diarrhea that is of rapid onset and course characterized by frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide
 * DOID:0050140
 * acute diffuse nephritis
 * class of disease
 * diffuse glomerulonephritis
 * Human disease
 * DOID:14066
 * acute disseminated encephalomyelitis
 * class of disease
 * encephalomyelitis
 * encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin
 * DOID:639
 * C10.114.375.225 C10.228.140.695.562.225 C10.314.350.225 C20.111.258.250.350 C23.550.291.500.829.188
 * acute endometritis
 * class of disease
 * endometritis
 * Human disease
 * DOID:7528
 * acute erythroid leukemia
 * class of disease
 * acute myeloid leukemia
 * rare form of acute myeloid leukemia (less than 5% of AML cases) where the myeloproliferation is of erythroblastic precursors.
 * DOID:0080780
 * C04.557.337.539.275.325 C15.378.190.636.276
 * Acute erythroid leukemia
 * acute ethmoiditis
 * class of disease
 * ethmoid sinusitis acute disease
 * ethmoid sinusitis which lasts for less than 4 weeks
 * DOID:9506
 * acute eustachian salpingitis
 * class of disease
 * otosalpingitis
 * otosalpingitis with a sudden onset and a short course
 * DOID:10550
 * acute female pelvic peritonitis
 * class of disease
 * peritonitis pelvic inflammatory diseases
 * Human disease
 * DOID:9978
 * acute frontal sinusitis
 * class of disease
 * frontal sinusitis acute disease
 * frontal sinusitis which lasts for less than 4 weeks
 * DOID:14225
 * acute gonococcal cervicitis
 * class of disease
 * acute cervicitis gonococcal infectious diseases
 * Human disease
 * DOID:10615
 * acute gonococcal cystitis
 * class of disease
 * urinary tract infection gonococcal infectious diseases
 * Human disease
 * DOID:13690
 * acute gonococcal endometritis
 * class of disease
 * acute endometritis gonococcal infectious diseases
 * Human disease
 * DOID:7527
 * acute gonococcal epididymo-orchitis
 * class of disease
 * epididymo-orchitis
 * Human disease
 * DOID:10802
 * acute gonococcal prostatitis
 * class of disease
 * prostatitis gonococcal infectious diseases
 * Human disease
 * DOID:13943
 * acute gonococcal salpingitis
 * class of disease
 * acute salpingitis gonococcal infectious diseases
 * Human disease
 * DOID:13942
 * acute hemorrhagic leukoencephalitis
 * class of disease
 * acute disseminated encephalomyelitis acute hemorrhagic encephalitis acute necrotizing encephalitis
 * very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema
 * DOID:10992
 * C10.114.375.225.500 C10.114.375.362 C10.228.140.695.562.225.500 C10.228.140.695.562.375 C10.314.350.225.500 C10.314.350.375 C20.111.258.250.350.500 C20.111.258.250.425
 * acute hemorrhagic pancreatitis
 * class of disease
 * acute pancreatitis
 * human disease
 * DOID:0080999
 * C06.689.750.325
 * acute hydrops keratoconus
 * class of disease
 * keratoconus eye disease
 * Human disease
 * DOID:10125
 * Corneal hydrops
 * acute infantile liver failure-multisystemic involvement syndrome
 * class of disease
 * liver failure, infantile autosomal recessive disease
 * human disease
 * DOID:0080717
 * acute infection of pinna
 * class of disease
 * otitis externa
 * Human disease
 * DOID:10520
 * acute inflammation of lacrimal passage
 * class of disease
 * lacrimal apparatus disease
 * Human disease
 * DOID:6970
 * acute kidney tubular necrosis
 * class of disease
 * acute kidney injury disease
 * medical condition involving the death of tubular epithelial cells that form the renal tubules of the kidneys
 * DOID:12556
 * C12.050.351.968.419.780.050.500 C12.200.777.419.780.050.500 C12.950.419.780.050.500
 * acute laryngitis
 * class of disease
 * laryngitis
 * respiratory disease
 * DOID:9396
 * acute laryngopharyngitis
 * class of disease
 * upper respiratory tract disease laryngopharyngitis
 * respiratory disease
 * DOID:11195
 * acute leukemia
 * class of disease
 * leukemia lymphoblastic leukemia disease
 * human disease
 * DOID:12603
 * Acute leukemias
 * acute lymphocytic leukemia
 * class of disease
 * acute leukemia lymphoblastic leukemia disease
 * leukemia that is characterized by over production of lymphoblasts.
 * DOID:9952
 * Acute lymphoblastic leukemia
 * Acute leukemia-ALL.jpg
 * acute maxillary sinusitis
 * class of disease
 * maxillary sinusitis acute disease
 * maxillary sinusitis which lasts for less than 4 weeks
 * DOID:2050
 * acute megakaryoblastic leukemia
 * class of disease
 * acute myeloid leukemia leukemia bilineal acute myeloid leukemia
 * leukemia that derives from blood-forming tissue in which megakaryocytes proliferate in the bone marrow and circulate in the blood in large numbers
 * DOID:8761
 * C04.557.337.539.275.450
 * acute monocytic leukemia
 * class of disease
 * monocytic leukemia acute myeloid leukemia disease
 * Human disease
 * DOID:8864
 * C04.557.337.539.275.484
 * Acute monocytic leukemia
 * acute myeloid leukemia
 * class of disease
 * acute leukemia myeloid leukemia disease
 * myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells
 * DOID:9119
 * C04.557.337.539.275
 * Acute myeloid leukemia
 * Auer rods.PNG
 * acute myeloid leukemia with BCR-ABL1
 * class of disease
 * acute myeloid leukemia
 * human disease
 * DOID:0080976
 * acute myocardial infarction
 * class of disease
 * myocardial infarction acute coronary syndrome
 * human disease
 * DOID:9408
 * acute myocarditis
 * class of disease
 * myocarditis
 * human disease
 * DOID:3951
 * acute necrotizing encephalitis
 * class of disease
 * encephalitis
 * Human disease
 * DOID:5222
 * acute orbital inflammation
 * class of disease
 * orbital disease inflammation
 * human disease
 * DOID:11230
 * acute pancreatitis
 * class of disease
 * pancreatitis disease
 * Human disease
 * DOID:2913
 * Acute pancreatitis
 * 3D Medical Animation Acute Pancreatitis.jpg
 * acute pericementitis
 * class of disease
 * periodontitis
 * Human disease
 * DOID:10423
 * acute perichondritis of pinna
 * class of disease
 * perichondritis of auricle
 * human disease
 * DOID:221
 * acute poststreptococcal glomerulonephritis
 * class of disease
 * glomerulonephritis
 * Human disease
 * DOID:14064
 * acute proliferative glomerulonephritis
 * class of disease
 * glomerulonephritis proliferative glomerulonephritis disease
 * Human disease
 * DOID:13138
 * Acute proliferative glomerulonephritis
 * acute promyelocytic leukemia
 * class of disease symptom or sign
 * acute myeloid leukemia bilineal acute myeloid leukemia disease
 * acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17
 * DOID:0060318
 * C04.557.337.539.275.700
 * Acute promyelocytic leukemia
 * Жедел промиелоцитарлы лейкоз (миелограмма).jpg
 * acute pulmonary heart disease
 * class of disease
 * cor pulmonale
 * Human disease
 * DOID:8514
 * acute retinal necrosis syndrome
 * class of disease
 * retinitis
 * Human disease
 * DOID:3611
 * C11.768.773.674
 * acute retrobulbar neuritis
 * class of disease
 * optic neuritis
 * Human disease
 * DOID:14155
 * acute salpingitis
 * class of disease
 * salpingitis
 * Human disease
 * DOID:10973
 * acute salpingo-oophoritis
 * class of disease
 * salpingo-oophoritis acute salpingitis
 * Human disease
 * DOID:10971
 * acute serous otitis media
 * class of disease
 * acute transudative otitis media serous glue ear
 * acute transudative otitis media with thin, watery and sterile effusion
 * DOID:11557
 * acute sphenoidal sinusitis
 * class of disease
 * sphenoid sinusitis acute disease
 * sphenoid sinusitis which lasts for less than 4 weeks
 * DOID:13046
 * acute stress disorder
 * class of disease
 * anxiety disorder stress-related disorders disease
 * psychological response to a terrifying, traumatic, or surprising experience
 * DOID:6088
 * F03.950.750.550
 * acute thyroiditis
 * class of disease
 * thyroiditis
 * Human disease
 * DOID:14353
 * acute tympanitis
 * class of disease
 * tympanic membrane disease myringitis
 * Human disease
 * DOID:13790
 * acute vascular insufficiency of intestine
 * class of disease
 * intestinal disease
 * Human disease
 * DOID:8590
 * adamantinoid basal cell epithelioma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4290
 * adamantinoma
 * class of disease
 * bone cancer disease
 * bone cancer that is located in almost exclusively in the long bones
 * DOID:2776
 * C04.588.149.030 C05.116.231.030
 * Adamantinoma
 * adamantinous craniopharyngioma
 * class of disease
 * craniopharyngioma
 * Human disease
 * DOID:3846
 * adenocarcinoma
 * class of disease
 * carcinoma disease
 * carcinoma that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue
 * DOID:299
 * C04.557.470.200.025
 * Adenocarcinomas
 * Adenocarcinoma of the Sigmoid Colon (longitudinal section, closeup).jpg
 * adenocarcinoma in situ
 * class of disease
 * in situ carcinoma adenocarcinoma
 * Human disease
 * DOID:4943
 * C04.557.470.200.025.014 C04.557.470.200.240.124 C23.149.249
 * adenocarcinoma of the lung
 * class of disease
 * lung cancer adenocarcinoma
 * non-small cell lung carcinoma that derives from epithelial cells of glandular origin
 * DOID:3910
 * C04.557.470.200.025.022 C04.588.894.797.520.055
 * adenofibroma
 * class of disease
 * benign neoplasms by histologic type fibroma
 * cell type benign neoplasm that is composed of glandular and fibrous tissues, with a relatively large proportion of glands
 * DOID:2683
 * C04.557.450.565.590.595.050 C04.557.470.625.050
 * adenoid basal cell carcinoma
 * class of disease
 * basal-cell carcinoma tonsil cancer
 * Human disease
 * DOID:4294
 * adenoid cystic carcinoma
 * class of disease
 * cancer cylindroma carcinoma tonsil cancer
 * type of cancer
 * DOID:0080202
 * C04.557.470.200.025.220
 * Adenoid cystic carcinoma
 * Adenoid cystic carcinoma - intermed mag.jpg
 * adenoid hypertrophy
 * class of disease
 * upper respiratory tract disease
 * upper respiratory tract disease characterized by the unusual growth of the adenoid tonsil; has symptom snoring, has symptom hyponasality, has symptom otitis media with effusion, has symptom mouth breathing
 * DOID:0060311
 * Adenoid hypertrophy
 * Adenoid hypertrophy.jpg
 * adenoiditis
 * class of disease
 * upper respiratory tract disease nasopharyngitis
 * inflammation of the adenoid tissue
 * DOID:0050145
 * adenoma
 * class of disease
 * benign neoplasms by histologic type disease
 * cell type benign neoplasm that is composed of epithelial tissue in which tumor cells form glands or glandlike structures
 * DOID:657
 * C04.557.470.035
 * Adenomas
 * Colon adenoma (1).jpg
 * adenomatoid tumor
 * class of disease
 * benign neoplasm benign mesothelioma
 * type of tumor
 * DOID:746
 * C04.557.470.035.200 C04.557.470.660.200
 * Adenomatoid tumors
 * adenomyoma
 * class of disease
 * carcinosarcoma carcinoma
 * carcinosarcoma that has material basis in gland and muscle components
 * DOID:2609
 * C04.557.435.110
 * Adenomyomas
 * adenomyoma of uterine corpus
 * class of disease
 * adenomyoma uterine corpus cancer carcinosarcoma of the corpus uteri uterine benign neoplasm
 * Human disease
 * DOID:4994
 * adenomyosis
 * class of disease
 * endometriosis uterine disease disease
 * extension of endometrial tissue into the myometrium
 * DOID:288
 * C13.351.500.852.113
 * Adenomyosis of the uterus
 * adenosarcoma
 * class of disease
 * carcinosarcoma
 * carcinosarcoma that derives from simultaneously or consecutively in mesodermal tissue and glandular epithelium
 * DOID:1974
 * C04.557.435.135 C04.557.450.795.135
 * adenosquamous bile duct carcinoma
 * class of disease
 * squamous cell carcinoma bile duct cancer
 * human disease
 * DOID:5624
 * adenosquamous breast carcinoma
 * class of disease
 * breast squamous cell carcinoma adenosquamous carcinoma breast cancer squamous cell carcinoma
 * Human disease
 * DOID:5623
 * adenosquamous carcinoma
 * class of disease
 * squamous cell carcinoma disease
 * squamous cell carcinoma that contains squamous cells and gland-like cells
 * DOID:4830
 * C04.557.435.250 C04.557.470.200.150
 * Adenosquamous carcinoma
 * adenosquamous cell lung carcinoma
 * class of disease
 * adenosquamous carcinoma squamous cell carcinoma of the lung squamous cell carcinoma lung cancer
 * Human disease
 * DOID:4829
 * adenosquamous gallbladder carcinoma
 * class of disease
 * gallbladder squamous cell carcinoma adenosquamous carcinoma squamous cell carcinoma gallbladder cancer gallbladder carcinoma
 * gallbladder carcinoma that derives from squamous cells and gland-like cells
 * DOID:5627
 * adenosquamous pancreas carcinoma
 * class of disease
 * adenosquamous carcinoma squamous cell carcinoma of pancreas squamous cell carcinoma pancreatic cancer
 * pancreatic ductal carcinoma that derives from squamous cells and gland-like cells
 * DOID:5637
 * adenosquamous prostate carcinoma
 * class of disease
 * adenosquamous carcinoma squamous cell carcinoma prostate cancer
 * prostate carcinoma that derives from squamous cells and gland-like cells
 * DOID:5634
 * adenoviral keratoconjunctivitis
 * class of disease
 * viral conjunctivitis keratoconjunctivitis adenovirus infection
 * common and highly contagious viral infection of the eye
 * DOID:13014
 * Adenoviral keratoconjunctivitis
 * adhesions of uterus
 * class of disease
 * gynatresia uterine disease disease
 * adhesions or fibrosis of endometrium of uterus
 * DOID:13812
 * Asherman's syndrome
 * adhesive otitis media
 * class of disease
 * ear disease otitis media adhesive middle ear disease
 * An auditory system disease that is characterized by a thin retracted ear drum becomes sucked into the middle-ear space and stuck (i.e., adherent) to the ossicles and other bones of the middle ear.
 * DOID:11235
 * adiposis dolorosa
 * class of disease
 * lipomatosis subcutaneous tissue disease
 * rare condition characterized by generalized obesity and fatty tumors in the adipose tissue.
 * DOID:3928
 * C17.800.463.249 C18.452.584.718.500
 * Adiposis dolorosa
 * Nervous and mental diseases (1919) (14781727145).jpg
 * adjustment disorder
 * class of disease
 * mental disorder disease
 * human disease
 * DOID:507
 * F03.950.500
 * Adjustment disorder
 * adolescence-adult electroclinical syndrome
 * class of disease
 * electroclinical syndrome absence seizure
 * electroclinical syndrome with onset in adolescence and adulthood
 * DOID:0050705
 * adrenal adenoma
 * class of disease
 * endocrine organ benign neoplasm adrenal gland disease benign epithelial neoplasm benign neoplasm of adrenal gland adenoma disease
 * endocrine organ benign neoplasm, a benign tumor of the glandular type (adenoma) in the adrenal gland
 * DOID:656
 * adrenal carcinoma
 * class of disease
 * adrenal gland cancer carcinoma
 * adrenal cancer that is located in the cortex (steroid hormone-producing tissue) of the adrenal gland and that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:3950
 * adrenal cortex cancer
 * class of disease
 * adrenal gland cancer adrenal cortex neoplasm adrenal cortex disease
 * Human disease
 * DOID:660
 * Cancers of adrenal glands
 * adrenal cortex disease
 * class of disease
 * adrenal gland disease
 * disease involving the adrenal cortex
 * DOID:3952
 * C19.053.098
 * adrenal cortical adenocarcinoma
 * class of disease
 * adrenocortical carcinoma adenocarcinoma
 * adrenalcortical carcinoma that originating in the cortex of the adrenal gland and derives from epithelial cells of glandular origin
 * DOID:3959
 * adrenal cortical hypofunction
 * class of disease
 * adrenal cortex disease primary adrenal insufficiency
 * Human disease
 * DOID:10493
 * adrenal gland cancer
 * class of disease
 * endocrine gland cancer adrenal gland neoplasm adrenal gland disease
 * endocrine gland cancer located in the adrenal glands which are located above the kidneys
 * DOID:3953
 * adrenal gland disease
 * class of disease
 * endocrine system disease
 * endocrine disease
 * DOID:9553
 * C19.053
 * Diseases and disorders of adrenal glands/hormones
 * adrenal gland ganglioneuroblastoma
 * class of disease
 * adrenal gland cancer adrenal neuroblastoma peripheral nervous system ganglioneuroblastoma malignant peripheral nerve neoplasm
 * Human disease
 * DOID:8140
 * adrenal gland hyperfunction
 * class of disease
 * adrenal cortex disease
 * Human disease
 * DOID:3947
 * C19.053.800
 * adrenal gland pheochromocytoma
 * class of disease
 * phaeochromocytoma malignant pheochromocytoma
 * adrenal medulla cancer that is characterized by overproduction of adrenaline
 * DOID:0050892
 * adrenal medulla cancer
 * class of disease
 * adrenal gland cancer adrenal medulla neoplasm
 * adrenal gland cancer that is located in the adrenal medulla
 * DOID:5719
 * adrenal medulla carcinoma
 * class of disease
 * adrenal medulla cancer carcinoma
 * adrenal medulla cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:7379
 * adrenal neuroblastoma
 * class of disease
 * adrenal gland cancer nervous system cancer adrenal medulla cancer endocrine gland cancer neuroblastoma
 * adrenal gland cancer that derives from immature neuroblastic cells
 * DOID:5718
 * Neuroblastoma of the adrenal glands
 * adrenal rest tumor
 * class of disease
 * endocrine organ benign neoplasm
 * Human disease
 * DOID:1786
 * C04.557.470.035.232
 * adrenocortical adenoma
 * class of disease
 * adrenal adenoma
 * adrenal adenoma that is a benign tumor of the adrenal cortex
 * DOID:0050891
 * C04.588.322.078.265.500 C19.053.098.265.500 C19.053.347.500.500 C19.344.078.265.500
 * Adrenocortical adenoma
 * adult acute lymphocytic leukemia
 * class of disease
 * acute lymphocytic leukemia
 * Human disease
 * DOID:5604
 * adult acute monocytic leukemia
 * class of disease
 * acute monocytic leukemia
 * acute monocytic leukemia occurring in adults
 * DOID:0080149
 * adult astrocytic tumour
 * class of disease
 * astrocytoma
 * Human disease
 * DOID:3076
 * adult botryoid rhabdomyosarcoma
 * class of disease
 * botryoid embryo rhabdomyosarcoma
 * Human disease
 * DOID:6847
 * adult brain ependymoma
 * class of disease
 * brain ependymoma
 * Human disease
 * DOID:7750
 * adult brain stem glioma
 * class of disease
 * Brainstem glioma brain stem cancer
 * Human disease
 * DOID:4813
 * adult brainstem astrocytoma
 * class of disease
 * adult brain stem glioma brain stem astrocytic neoplasm
 * Human disease
 * DOID:5922
 * adult brainstem gliosarcoma
 * class of disease
 * adult brain stem glioma
 * human disease
 * DOID:4812
 * adult brainstem mixed glioma
 * class of disease
 * adult brain stem glioma
 * Human disease
 * DOID:5921
 * adult central nervous system choriocarcinoma
 * class of disease
 * choriocarcinoma central nervous system cancer central nervous system adult germ cell tumor central nervous system choriocarcinoma nervous system cancer central nervous system disease
 * Human disease
 * DOID:6634
 * adult central nervous system embryonal carcinoma
 * class of disease
 * central nervous system adult germ cell tumor central nervous system embryonal carcinoma
 * Human disease
 * DOID:7233
 * adult central nervous system germinoma
 * class of disease
 * central nervous system germinoma central nervous system adult germ cell tumor
 * Human disease
 * DOID:7867
 * adult central nervous system immature teratoma
 * class of disease
 * adult central nervous system teratoma central nervous system immature teratoma
 * Human disease
 * DOID:6018
 * adult central nervous system mature teratoma
 * class of disease
 * adult central nervous system teratoma central nervous system mature teratoma
 * Human disease
 * DOID:6016
 * adult central nervous system mixed germ cell tumor
 * class of disease
 * central nervous system adult germ cell tumor mixed germ cell tumor of central nervous system
 * Human disease
 * DOID:7945
 * adult central nervous system primitive neuroectodermal neoplasm
 * class of disease
 * central nervous system primitive neuroectodermal neoplasm
 * Human disease
 * DOID:3865
 * adult central nervous system teratoma
 * class of disease
 * central nervous system teratoma central nervous system adult germ cell tumor
 * Human disease
 * DOID:6015
 * adult cerebellar neoplasm
 * class of disease
 * cerebellum cancer
 * Human disease
 * DOID:5056
 * adult choroid plexus cancer
 * class of disease
 * choroid plexus neoplasm
 * Human disease
 * DOID:3542
 * adult cystic teratoma
 * class of disease
 * cystic teratoma
 * Human disease
 * DOID:7079
 * adult dermatomyositis
 * class of disease
 * dermatomyositis
 * Dermatomyositis in an adult
 * DOID:14202
 * adult endodermal sinus tumor
 * class of disease
 * endodermal sinus tumor
 * endodermal sinus tumor that occurs in adults
 * DOID:5348
 * adult ependymoblastoma
 * class of disease
 * ependymoblastoma adult central nervous system primitive neuroectodermal neoplasm
 * Human disease
 * DOID:7631
 * adult epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma
 * Human disease
 * DOID:8282
 * adult extraosseous chondrosarcoma
 * class of disease
 * extraosseous chondrosarcoma
 * Human disease
 * DOID:7902
 * adult extraosseous osteosarcoma
 * class of disease
 * bone cancer extraosseous osteosarcoma osteosarcoma
 * adult sarcoma of soft tissue and extraosseous osteosarcoma that is located in the soft tissues without direct attachment to the skeletal system and results in the production of osteoid, bone, or chondroid material
 * DOID:7827
 * adult familial myoclonic epilepsy 1
 * class of disease
 * benign adult familial myoclonic epilepsy autosomal dominant disease
 * human disease
 * DOID:0111690
 * adult familial myoclonic epilepsy 3
 * class of disease
 * benign adult familial myoclonic epilepsy autosomal dominant disease
 * human disease
 * DOID:0111695
 * adult fibrosarcoma
 * class of disease
 * fibrosarcoma conventional fibrosarcoma
 * Human disease
 * DOID:3516
 * adult hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma
 * hepatocellular carcinoma is characterized by hepatic mass, abdominal pain and, in advanced stages, jaundice, cachexia and liver failure and often develops in the setting of chronic necro-inflammation
 * DOID:0070328
 * adult hypophosphatasia
 * class of disease
 * hypophosphatasia
 * A hypophosphatasia that has material basis in a heterozygous mutation of ALPL on chromosome 1p36.12.
 * DOID:0110913
 * adult infiltrating astrocytic neoplasm
 * class of disease
 * adult astrocytic tumour
 * Human disease
 * DOID:7656
 * adult intracranial malignant hemangiopericytoma
 * class of disease
 * connective tissue neoplasm
 * Human disease
 * DOID:6333
 * adult leptomeningeal melanoma
 * class of disease
 * meningeal melanoma
 * Human disease
 * DOID:6090
 * adult liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5693
 * adult lymphoma
 * class of disease
 * lymphoma
 * Human disease
 * DOID:5825
 * adult malignant hemangiopericytoma
 * class of disease
 * hemangiopericytoma hemangiopericytoma, malignant
 * Human disease
 * DOID:6332
 * adult malignant mesenchymoma
 * class of disease
 * malignant mesenchymoma
 * Human disease
 * DOID:5894
 * adult malignant schwannoma
 * class of disease
 * malignant peripheral nerve sheath tumor childhood malignant schwannoma
 * Human disease
 * DOID:8369
 * adult medulloblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3864
 * adult mesenchymal chondrosarcoma
 * class of disease
 * mesenchymal chondrosarcoma
 * adult sarcoma of soft tissue and mesenchymal chondrosarcoma that is located in the cartilage
 * DOID:4547
 * adult myxoid chondrosarcoma
 * class of disease
 * myxoid chondrosarcoma
 * adult sarcoma of soft tissue and myxoid chondrosarcoma that is composed of multiple lobules of chondroblast-like cells, arranged in cords and strands, embedded in a myxoid stroma, and separated by fibrous septa
 * DOID:6495
 * adult oligodendroglioma
 * class of disease
 * oligodendroglioma
 * Human disease
 * DOID:3186
 * adult papillary meningioma
 * class of disease
 * rhabdoid meningioma papillary meningioma
 * Human disease
 * DOID:7826
 * adult pineal parenchymal tumor
 * class of disease
 * pinealoma
 * Human disease
 * DOID:5031
 * adult pineoblastoma
 * class of disease
 * adult pineal parenchymal tumor pinealoblastoma
 * Human disease
 * DOID:6648
 * adult pleomorphic rhabdomyosarcoma
 * class of disease
 * pleomorphic rhabdomyosarcoma
 * Human disease
 * DOID:8251
 * adult spinal cord ependymoma
 * class of disease
 * spinal cord ependymoma
 * Human disease
 * DOID:7788
 * adult spinal cord glioblastoma multiforme
 * class of disease
 * spinal cord glioma
 * Human disease
 * DOID:7806
 * adult teratoma
 * class of disease
 * teratoma benign teratoma
 * Human disease
 * DOID:5565
 * adult type testicular granulosa cell tumor
 * class of disease
 * testicular granulosa cell tumor
 * Human disease
 * DOID:8394
 * adult vagina botryoid rhabdomyosarcoma
 * class of disease
 * vagina botryoid rhabdomyosarcoma adult botryoid rhabdomyosarcoma
 * Human disease
 * DOID:6848
 * adult xanthogranuloma
 * class of disease
 * non-Langerhans-cell histiocytosis xanthogranuloma
 * Human disease
 * DOID:7875
 * adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
 * class of disease
 * leukodystrophy autosomal dominant disease Leukoencephalopathy with neuroaxonal spheroids
 * leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has material basis in heterozygous mutation in the CSF1R gene on chromosome 5q32
 * DOID:0080523
 * adult-onset severe asthma
 * class of disease
 * chronic asthma
 * human disease
 * DOID:0080816
 * adult-onset type II citrullinemia
 * class of disease
 * citrullinemia
 * human disease
 * DOID:0070342
 * advanced sleep phase syndrome 1
 * class of disease
 * advanced sleep phase syndrome
 * advanced sleep phase syndrome that has material basis in heterozygous mutation in the PER2 gene on chromosome 2q37
 * DOID:0110011
 * afferent loop syndrome
 * class of disease
 * postgastrectomy syndrome
 * Human disease
 * DOID:8438
 * C06.405.469.531.099 C23.550.767.050
 * aflatoxins-related hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma
 * Human disease
 * DOID:5022
 * agammaglobulinemia 5
 * class of disease
 * autosomal dominant disease agammaglobulinemia
 * human disease
 * DOID:0080588
 * age related macular degeneration 1
 * class of disease
 * age related macular degeneration
 * human disease
 * DOID:0110014
 * age related macular degeneration 10
 * class of disease
 * age related macular degeneration hereditary retinal dystrophy
 * An age related macular degeneration associated with variation in the genomic region 9:112,100,000-127,500,000 (GRCh38). TLR4 has been put forth as a candidate gene.
 * DOID:0110022
 * age related macular degeneration 13
 * class of disease
 * age related macular degeneration hereditary retinal dystrophy
 * age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25
 * DOID:0110025
 * age related macular degeneration 14
 * class of disease
 * age related macular degeneration hereditary retinal dystrophy
 * age related macular degeneration associated with variation at or near the C2 and CFB genes on chromosome 6p21
 * DOID:0110026
 * age related macular degeneration 15
 * class of disease
 * age related macular degeneration hereditary retinal dystrophy
 * age related macular degeneration conferred by variation in the C9 gene on chromosome 5p13
 * DOID:0110027
 * age related macular degeneration 5
 * class of disease
 * age related macular degeneration hereditary retinal dystrophy
 * age related macular degeneration onferred by heterozygous mutation in the ERCC6 gene on chromosome 10q11
 * DOID:0110028
 * aggressive digital papillary adenocarcinoma
 * class of disease
 * papillary adenocarcinoma skin carcinoma adenocarcinoma sweat gland carcinoma
 * medical condition
 * DOID:5590
 * aggressive periodontitis
 * class of disease
 * periodontitis
 * periodontitis characterized by rapid attachment loss and bone destruction
 * DOID:1474
 * C07.465.714.533.161
 * aggressive systemic mastocytosis
 * class of disease
 * systemic mastocytosis
 * Human disease
 * DOID:4798
 * agoraphobia
 * class of disease
 * phobia disease
 * phobic disorder involving the specific anxiety about being in a place or situation where escape is difficult or embarrassing or where help may be unavailable
 * DOID:593
 * F03.080.100
 * agraphia
 * class of disease symptom or sign
 * writing disorder aphasia disease
 * disease that results in the loss of the ability to write
 * DOID:0060223
 * C10.597.606.150.500.050 C23.888.592.604.150.500.050 C10.597.606.150.550.700.125 C23.888.592.604.150.550.700.125 F03.625.374.188.700.125 F03.625.562.700.125
 * ainhum
 * class of disease
 * connective tissue disease foot diseases genetic disease autoamputation disease
 * Human disease
 * DOID:11329
 * C05.116.264.143
 * Ainhum
 * Ainhum.jpg
 * akinetic mutism
 * class of disease
 * encephalopathy
 * brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness
 * DOID:4267
 * C10.228.140.042
 * akinetopsia
 * class of disease
 * agnosia visual perception motion perception
 * agnosia that is a loss of motion perception
 * DOID:0060130
 * alastrim
 * class of disease
 * smallpox
 * milder form of smallpox
 * DOID:9153
 * alcohol abuse
 * class of disease
 * substance abuse alcohol consumption alcohol-related disorders
 * substance abuse that involves the recurring use of alcoholic beverages despite negative consequences
 * DOID:1574
 * Alcohol abuse
 * The Drunkard's Progress 1846.jpg
 * alcohol dependence
 * class of disease
 * non-controlled substance abuse alcoholism alcohol abuse
 * human disease
 * DOID:0050741
 * alcohol-induced mental disorder
 * class of disease
 * long-term effects of alcohol consumption non-controlled substance abuse substance-induced psychosis
 * nental and behavioural disorders due to use of alcohol
 * DOID:251
 * alcohol-induced psychotic disorder
 * class of disease
 * alcohol-induced mental disorder substance-induced psychosis
 * organic psychotic states due mainly to excessive consumption of alcoholic beverages
 * DOID:252
 * C25.723.809.750 C25.775.100.087.750
 * alcohol-related birth defect
 * class of disease
 * fetal alcohol spectrum disorders
 * fetal alcohol spectrum disorder that results in damage to organs, bones, or muscles due to prenatal alcohol exposure
 * DOID:0050668
 * alcohol-related neurodevelopmental disorder
 * class of disease
 * fetal alcohol spectrum disorders
 * human disease
 * DOID:0050667
 * alcoholic cardiomyopathy
 * class of disease
 * extrinsic cardiomyopathy long-term effects of alcohol consumption alcohol and health
 * disease in which the chronic long-term abuse of alcohol (i.e., ethanol) leads to heart failure
 * DOID:12935
 * C14.280.238.057 C25.775.100.087.250
 * alcoholic gastritis
 * class of disease
 * gastritis long-term effects of alcohol consumption chronic gastritis
 * human disease
 * DOID:8680
 * alcoholic hepatitis
 * class of disease
 * hepatitis alcoholic liver disease disease
 * hepatitis (inflammation of the liver) due to excessive intake of alcohol
 * DOID:12351
 * C06.552.380.290 C06.552.645.490 C25.775.100.087.645.490
 * Alcoholic hepatitis
 * Mallory body high mag cropped.jpg
 * alcoholic liver cirrhosis
 * class of disease
 * liver cirrhosis alcoholic liver disease
 * Human disease
 * DOID:14018
 * C06.552.630.380 C06.552.645.590 C25.775.100.087.645.550
 * Alcoholic cirrhosis
 * alcoholic neuropathy
 * class of disease
 * inflammatory and toxic neuropathy polyneuropathy long-term effects of alcohol consumption nervous system alcohol-induced disorders disease
 * Human disease
 * DOID:14183
 * C10.668.829.800.050 C10.720.112.400 C25.723.705.150.400 C25.775.100.087.193.400
 * alcoholic pancreatitis
 * class of disease
 * pancreatitis long-term effects of alcohol consumption alcohol and health
 * human disease
 * DOID:4988
 * C06.689.750.660 C25.775.100.087.730
 * alcuronium bromide allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger alcuronium bromide
 * DOID:0040077
 * aleukemic leukemia
 * class of disease
 * leukemia
 * leukemia that arises from changes in the tissues forming white blood cells and characterized by a normal or decreased number of white blood cells in the circulating blood
 * DOID:6004
 * aleukemic leukemia cutis
 * class of disease
 * aleukemic leukemia Leukemia cutis
 * Human disease
 * DOID:6003
 * aleukemic monocytic leukemia cutis
 * class of disease
 * aleukemic leukemia cutis
 * Human disease
 * DOID:6958
 * alexithymia
 * class of disease
 * agnosia disease
 * subclinical deficiency in understanding, processing, or describing emotions
 * DOID:0060131
 * Autism Aspect Alexithymia 1.png
 * algoneurodystrophy
 * class of disease
 * complex regional pain syndrome
 * Human disease
 * DOID:14022
 * allergic asthma
 * class of disease
 * respiratory allergy asthma extrinsic asthma
 * asthma with a basis in a pathological type I hypersensitivity reaction
 * DOID:9415
 * Asthma
 * allergic conjunctivitis
 * class of disease symptom or sign
 * chronic conjunctivitis eye allergy allergy
 * chronic conjunctivitis that is an inflammation of the conjunctiva
 * DOID:11204
 * C11.187.183.200 C20.543.480.200
 * Allergic conjunctivitis
 * Allergicconjunctivitis.jpg
 * allergic contact dermatitis
 * class of disease
 * allergic dermatitis contact dermatitis disease
 * medical condition
 * DOID:3042
 * C17.800.174.255.100 C17.800.815.255.100 C20.543.418.150
 * Allergic contact dermatitis
 * allergic contact dermatitis of eyelid
 * class of disease
 * noninfectious dermatoses of eyelid allergic contact dermatitis Eyelid dermatitis
 * Human disease
 * DOID:1895
 * allergic rhinitis
 * class of disease symptom or sign
 * rhinitis respiratory allergy disease
 * human disease
 * DOID:4481
 * C08.460.799.315 C08.674.453 C09.603.799.315 C20.543.480.680.443
 * Allergic rhinitis
 * Misc pollen colorized.jpg
 * allescheriosis
 * class of disease
 * primary systemic mycosis Pseudallescheriasis
 * primary systemic mycosis that results in systemic fungal infection, has material basis in Pseudallescheria boydii, which results in formation of abscesses
 * DOID:11186
 * alopecia areata
 * class of disease symptom or sign
 * alopecia autoimmune disease autoimmune skin disease
 * condition in which hair is lost from some or all areas of the body
 * DOID:986
 * C17.800.329.937.122.147
 * Alopecia areata
 * Allopecia areata.JPG
 * alopecia-intellectual disability syndrome
 * class of disease
 * genetic syndromic intellectual disability syndrome
 * human disease
 * DOID:0080627
 * alopecia-mental retardation syndrome 1
 * class of disease
 * autosomal recessive disease alopecia-intellectual disability syndrome
 * human disease
 * DOID:0080628
 * alopecia-mental retardation syndrome 2
 * class of disease
 * alopecia-intellectual disability syndrome autosomal recessive disease
 * human disease
 * DOID:0080629
 * alopecia-mental retardation syndrome 4
 * class of disease
 * alopecia-intellectual disability syndrome autosomal recessive disease
 * human disease
 * DOID:0080950
 * alpha chain disease
 * class of disease
 * heavy chain disease intestinal neoplasm
 * heavy chain disease that results from an overproduction of alpha antibodies (IgA)
 * DOID:0060126
 * C04.557.386.390 C06.301.371.411.512 C06.405.249.411.512 C06.405.469.491.505 C15.378.147.780.490.512 C15.604.515.435.512 C20.683.515.512 C20.683.780.490.512
 * alpha-thalassemia-myelodysplastic syndrome
 * class of disease
 * Acquired hemolytic anemia alpha-thalassemia-related diseases myelodysplastic syndrome syndrome
 * human disease
 * DOID:0112125
 * alternating esotropia
 * class of disease
 * esotropia
 * Human disease
 * DOID:9888
 * alternating exotropia
 * class of disease
 * exotropia
 * Human disease
 * DOID:1142
 * alveolar osteitis
 * class of disease
 * periostitis disease
 * human disease
 * DOID:13585
 * C07.465.227
 * alveolar rhabdomyosarcoma
 * class of disease
 * rhabdomyosarcoma
 * human disease
 * DOID:4051
 * C04.557.450.590.550.660.665 C04.557.450.795.550.660.665
 * alveoli adenoma
 * class of disease
 * lung adenoma bronchial neoplasm benign neoplasms by histologic type adenoma
 * Human disease
 * DOID:8003
 * Alveolar adenoma
 * amblyopia
 * class of disease symptom or sign
 * eye disease visual impairment disease
 * human disease
 * DOID:10376
 * C10.228.140.055 C10.597.751.941.073 C11.966.073 C23.888.592.763.941.073
 * Amblyopia
 * Child eyepatch.jpg
 * amelanotic melanoma
 * class of disease
 * melanoma
 * human disease
 * DOID:4359
 * C04.557.465.625.650.510.515 C04.557.580.625.650.510.515 C04.557.665.510.515
 * amelogenesis imperfecta type 1B
 * class of disease
 * amelogenesis imperfecta autosomal dominant disease
 * amelogenesis imperfecta that has material basis in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13
 * DOID:0110052
 * amelogenesis imperfecta type 2A6
 * class of disease
 * amelogenesis imperfecta
 * human disease
 * DOID:0080960
 * amelogenesis imperfecta type 3B
 * class of disease
 * amelogenesis imperfecta autosomal dominant disease amelogenesis imperfecta type 3
 * human disease
 * DOID:0080243
 * amelogenesis imperfecta type 3C
 * class of disease
 * amelogenesis imperfecta type 3 autosomal recessive disease
 * human disease
 * DOID:0111722
 * amenorrhea
 * class of disease
 * female reproductive system disease hypomenorrhea disease
 * absence of a menstrual period in a woman of reproductive age
 * DOID:13938
 * C23.550.568.500
 * ametropic amblyopia
 * class of disease
 * amblyopia refractive error
 * Human disease
 * DOID:10377
 * amino acid metabolic disorder
 * class of disease
 * inherited metabolic disorder
 * inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids
 * DOID:9252
 * C16.320.565.100 C18.452.648.100
 * amnesia
 * class of disease symptom or sign
 * cognitive disorder memory disorder psychopathological syndrome disease
 * cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, continuous high blood pressure and severe shock may also cause amnesia
 * DOID:10914
 * C10.597.606.525.100 C23.888.592.604.529.100 F01.700.625.100 F03.615.200
 * Amnesie.jpg
 * amodiaquine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger amodiaquine
 * DOID:0040022
 * amoxicillin allergy
 * class of disease
 * beta-lactam allergy
 * beta-lactam allergy that has allergic trigger amoxicillin
 * DOID:0040004
 * amphetamine-related disorders
 * class of disease
 * substance abuse stimulant use disorder
 * negative health consequences of substance abuse that involves the recurring use of amphetamines
 * DOID:670
 * C25.775.225 F03.900.225
 * ampulla of Vater adenocarcinoma
 * class of disease
 * ampulla of Vater carcinoma duodenum adenocarcinoma extrahepatic bile duct adenocarcinoma adenocarcinoma
 * ampulla of Vater carcinoma that derives from epithelial cells of glandular origin
 * DOID:3502
 * ampulla of Vater adenosquamous carcinoma
 * class of disease
 * ampulla of Vater squamous cell carcinoma adenosquamous bile duct carcinoma squamous cell carcinoma ampulla of Vater cancer
 * ampulla of Vater carcinoma that derives from squamous cells and gland-like cells
 * DOID:5628
 * ampulla of Vater cancer
 * class of disease
 * duodenum cancer ampulla of Vater neoplasm bile duct cancer
 * Human disease
 * DOID:10020
 * ampulla of Vater carcinoma
 * class of disease
 * ampulla of Vater cancer small intestine carcinoma duodenum cancer extrahepatic bile duct carcinoma carcinoma
 * ampulla of Vater cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:4932
 * Carcinoma of the ampulla of Vater
 * ampulla of Vater clear cell adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma bile duct clear cell adenocarcinoma
 * Human disease
 * DOID:5308
 * ampulla of Vater mucinous adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma bile duct mucinous adenocarcinoma
 * Human disease
 * DOID:3693
 * ampulla of Vater neoplasm
 * class of disease
 * duodenal neoplasm bile duct disease biliary tract neoplasm
 * Human disease
 * DOID:10022
 * ampulla of Vater small cell carcinoma
 * class of disease
 * ampulla of Vater carcinoma liver neuroendocrine carcinoma small cell carcinoma
 * Human disease
 * DOID:7136
 * ampulla of Vater squamous cell carcinoma
 * class of disease
 * ampulla of Vater carcinoma squamous cell bile duct carcinoma squamous cell carcinoma of the small intestine squamous cell carcinoma
 * ampulla of Vater carcinoma that derives from epithelial squamous cells
 * DOID:5527
 * ampullary signet ring cell adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma bile duct signet ring cell carcinoma
 * Human disease
 * DOID:3501
 * amusia
 * class of disease
 * agnosia auditory agnosia music-specific disorders
 * loss of the ability to recognize musical notes, rhythms, and intervals
 * DOID:0060132
 * amyloid tumor
 * class of disease
 * mesenchymal cell neoplasm connective tissue benign neoplasm amyloidosis
 * Human disease
 * DOID:6755
 * amyloidosis
 * class of disease
 * systemic disease proteostasis deficiency acquired metabolic disease disease
 * metabolic disease involving abnormal deposited amyloid proteins
 * DOID:9120
 * C18.452.845.500
 * Amyloidosis
 * Small bowel duodenum with amyloid deposition congo red 10X.jpg
 * amyotrohpic lateral sclerosis type 22
 * class of disease
 * amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis that has material basis in mutation in the TUBA4A gene on chromosome 2q35
 * DOID:0060355
 * amyotrophic lateral sclerosis type 1
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * The most common type of familial ALS that has material basis in mutation in the SOD1 gene on chromosome 21
 * DOID:0060193
 * amyotrophic lateral sclerosis type 10
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis amyotrophic lateral sclerosis and frontotemporal dementia
 * human disease
 * DOID:0060201
 * amyotrophic lateral sclerosis type 11
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * human disease
 * DOID:0060202
 * amyotrophic lateral sclerosis type 12
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis that has material basis in mutation in the OPTN gene on chromosome 10
 * DOID:0060203
 * amyotrophic lateral sclerosis type 13
 * class of disease
 * amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis where a mutation that has material basis in the ATXN2 gene on chromosome 12 contributes to suscepitbility
 * DOID:0060204
 * amyotrophic lateral sclerosis type 14
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis amyotrophic lateral sclerosis and frontotemporal dementia
 * amyotrophic lateral sclerosis that has material basis in mutation in the VCP gene on chromosome 9
 * DOID:0060205
 * amyotrophic lateral sclerosis type 15
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis that has material basis in mutation in the UBQLN2 gene on chromosome X
 * DOID:0060206
 * amyotrophic lateral sclerosis type 18
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis that has material basis in mutation in the PFN1 gene on chromosome 17
 * DOID:0060209
 * amyotrophic lateral sclerosis type 19
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis that has material basis in mutation in the ERBB4 gene on chromosome 2
 * DOID:0060210
 * amyotrophic lateral sclerosis type 2
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * human disease
 * DOID:0060194
 * amyotrophic lateral sclerosis type 20
 * class of disease
 * amyotrophic lateral sclerosis familial amyotrophic lateral sclerosis
 * amyotrophic lateral sclerosis with juvenile onset that has material basis in mutation in the HNRNPA1 gene on chromosome 12
 * DOID:0060211
 * amyotrophic lateral sclerosis type 21
 * class of disease
 * amyotrophic lateral sclerosis nervous system heredodegenerative disease
 * amyotrophic lateral sclerosis that has material basis in mutation in the MATR3 gene on chromosome 5
 * DOID:0060212
 * amyotrophic lateral sclerosis type 23
 * class of disease
 * amyotrophic lateral sclerosis
 * human disease
 * DOID:0080225
 * amyotrophic lateral sclerosis type 3
 * class of disease
 * amyotrophic lateral sclerosis
 * human disease
 * DOID:0060195
 * amyotrophic lateral sclerosis type 6
 * class of disease
 * amyotrophic lateral sclerosis sporadic amyotrophic lateral sclerosis amyotrophic lateral sclerosis and frontotemporal dementia
 * human disease
 * DOID:0060198
 * amyotrophic lateral sclerosis type 7
 * class of disease
 * amyotrophic lateral sclerosis
 * human disease
 * DOID:0060199
 * amyotrophic lateral sclerosis type 8
 * class of disease
 * amyotrophic lateral sclerosis
 * human disease
 * DOID:0050752
 * amyotrophic lateral sclerosis type 9
 * class of disease
 * amyotrophic lateral sclerosis
 * human disease
 * DOID:0060200
 * amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
 * class of disease
 * neurodegeneration
 * A neurodegenerative disease characterized by chronic, progressive amyotrophic lateral sclerosis and parkinsonism-dementia. Susceptibility to this disease is influenced by heterozygous mutation in TRPM7 on 15q21.2.
 * DOID:0111246
 * amyotrophic neuralgia
 * class of disease
 * brachial plexus neuropathy neurodegeneration
 * human disease
 * DOID:10383
 * anaerobic meningitis
 * class of disease
 * bacterial meningitis anaerobic infection
 * human disease
 * DOID:14559
 * anal Buschke-Lowenstein tumor
 * class of disease
 * anal squamous cell carcinoma verrucous carcinoma giant condyloma acuminatum
 * Human disease
 * DOID:7175
 * anal Paget's disease
 * class of disease
 * anus adenocarcinoma extramammary Paget's disease rare genetic intestinal disease inherited digestive tract tumor rare epithelial tumor of rectum
 * Human disease
 * DOID:3446
 * Anal Paget's disease
 * anal canal Paget's disease
 * class of disease
 * anal canal adenocarcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:8119
 * anal canal adenocarcinoma
 * class of disease
 * anus adenocarcinoma anal canal cancer adenocarcinoma
 * anal canal cancer that derives from epithelial cells of glandular origin
 * DOID:3692
 * anal canal cancer
 * class of disease
 * large intestine cancer
 * large intestine cancer that is located in the terminal part of the large intestine
 * DOID:0050688
 * anal canal carcinoma
 * class of disease
 * carcinoma anal canal cancer
 * anal canal cancer that derives from epithelial cells
 * DOID:6126
 * anal canal squamous cell carcinoma
 * class of disease
 * squamous cell carcinoma anal squamous cell carcinoma anal canal cancer
 * anal canal cancer that derives from epithelial squamous cells
 * DOID:7177
 * anal cancer
 * class of disease
 * anus neoplasm anal canal cancer anal disease large intestine cancer disease
 * Is a rare disease which it is caused in most of the cases by the infection of the Human Papilloma Virus (HPV).
 * DOID:14110
 * Anal cancer
 * anal carcinoma
 * class of disease
 * anal cancer carcinoma
 * anus cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the anus
 * DOID:4908
 * anal carcinoma in situ
 * class of disease
 * anal carcinoma rectum carcinoma in situ in situ carcinoma Anal dysplasia
 * Human disease
 * DOID:9087
 * anal colloid adenocarcinoma
 * class of disease
 * anus adenocarcinoma rectum mucinous adenocarcinoma
 * anus carcinoma that derives from epithelial cells of glandular origin located in the anal colloid
 * DOID:3691
 * anal disease
 * class of disease
 * anorectal disorder rectal disease
 * human disease
 * DOID:3128
 * C06.405.469.860.101
 * Diseases and disorders of anus and anal canal
 * anal fistula
 * class of disease
 * rectal disease
 * anus disease characterized by an abnormal connection between the epithelialised surface of the anal canal and the perianal skin
 * DOID:0060328
 * C06.267.550.600 C06.405.469.471.600 C06.405.469.860.752 C23.300.575.185.550.600
 * Anal fistula
 * anal gland adenocarcinoma
 * class of disease
 * anus adenocarcinoma
 * anus carcinoma that derives from epithelial cells of glandular origin located in the anal gland
 * DOID:7531
 * anal margin basal cell carcinoma
 * class of disease
 * anal margin carcinoma basal-cell carcinoma
 * Human disease
 * DOID:4283
 * anal margin carcinoma
 * class of disease
 * anal carcinoma skin carcinoma skin cancer
 * anal carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the anal margin (where the canal meets the outside skin at the anus)
 * DOID:4284
 * anal margin squamous cell carcinoma
 * class of disease
 * anal margin carcinoma squamous cell carcinoma
 * Human disease
 * DOID:12239
 * anal neuroendocrine tumor
 * class of disease
 * anus neoplasm rectum neuroendocrine neoplasm
 * Human disease
 * DOID:5545
 * anal spasm
 * class of disease
 * anal disease
 * Human disease
 * DOID:11374
 * anal squamous cell carcinoma
 * class of disease
 * anal carcinoma rectum squamous cell carcinoma squamous cell carcinoma
 * anal carcinoma that arises near the squamocolumnar junction
 * DOID:5525
 * anal stricture
 * class of disease
 * anorectal anomalies anal disease
 * human disease
 * DOID:11014
 * C06.198.025 C16.131.314.047
 * anaplastic astrocytoma
 * class of disease
 * astrocytoma
 * astrocytoma that is characterized by cells with regular, round to oval nuclei
 * DOID:3078
 * Anaplastic astrocytoma
 * 405518-FIBRILLARY OR DIFFUSE ASTROCYTIC NEOPLASM.jpg
 * anaplastic ependymoma
 * class of disease
 * ependymoma grade III glioma
 * Human disease
 * DOID:5889
 * Anaplastic ependymoma
 * anaplastic large-cell lymphoma
 * class of disease
 * T-cell lymphoma non-Hodgkin lymphoma
 * non-Hodgkin lymphoma involving aberrant T-cells
 * DOID:0050744
 * C04.557.386.480.750.399 C15.604.515.569.480.750.600 C20.683.515.761.480.750.399
 * anaplastic oligodendroglioma
 * class of disease
 * oligodendroglioma
 * human disease
 * DOID:7154
 * Anaplastic oligodendroglioma
 * Oligodendroglioma 003.jpg
 * anaplastic thyroid cancer
 * class of disease
 * thyroid cancer large cell carcinoma undifferentiated carcinoma thyroid carcinoma
 * form of thyroid cancer
 * DOID:0080522
 * anatomical narrow angle borderline glaucoma
 * class of disease
 * borderline glaucoma chronic closed-angle glaucoma
 * Human disease
 * DOID:13327
 * anauxetic dysplasia
 * class of disease
 * spondyloepimetaphyseal dysplasia
 * human disease
 * DOID:0080942
 * anauxetic dysplasia 2
 * class of disease
 * autosomal recessive disease anauxetic dysplasia
 * human disease
 * DOID:0080962
 * androgen insensitivity syndrome
 * class of disease
 * pseudohermaphroditism sex differentiation disease disease
 * sex differentiation condition involving hormonal resistance due to androgen receptor dysfunction in a karyotypically male person
 * DOID:4674
 * C12.706.316.096.500 C13.351.875.253.096.500 C16.131.939.316.096.500 C16.320.322.061 C19.391.119.096.500
 * Androgen insensitivity syndrome
 * Women with androgen insensitivity syndrome.jpg
 * androgenic alopecia
 * class of disease
 * baldness androgen-dependent syndrome disease
 * hair loss due to susceptibility of hair follicles to androgenic miniaturization
 * DOID:0050801
 * Androgenic alopecia
 * Male pattern baldness.jpg
 * anemia
 * class of disease symptom or sign
 * hematopoietic system disease cytopenia hemic system symptom disease
 * decrease in number of red blood cells
 * DOID:2355
 * C15.378.071
 * Anemias
 * AnemiaFrote.jpg
 * anemia of prematurity
 * class of disease
 * neonatal anemia premature infant disease
 * Human disease
 * DOID:11243
 * anencephaly
 * class of disease
 * nervous system malformations disease
 * absence of a major portion of the brain, skull, and scalp that occurs during embryonic development
 * DOID:0060668
 * C10.500.680.196 C16.131.085.197 C16.131.666.680.196
 * Anencephaly
 * Anencephaly-web.jpg
 * aneruptive fever
 * class of disease
 * spotted fever
 * A spotted fever that has material basis in Rickettsia helvetica, which is transmitted by ticks (Ixodes sp). The infection has symptom fever, has symptom headache, has symptom myalgia.
 * DOID:0050484
 * aneurysm of heart
 * class of disease
 * heart disease aneurysm disease
 * Human disease
 * DOID:9768
 * C14.280.358 C14.907.055.608
 * Heart aneurysms
 * aneurysm-osteoarthritis syndrome
 * class of disease
 * Loeys-Dietz syndrome
 * human disease
 * DOID:0070237
 * angiodysplasia
 * class of disease
 * vascular disease disease
 * vascular disease that is characterized as a small vascular malformation of the gut
 * DOID:2494
 * C14.907.075
 * Angiodysplasia
 * Argon plasma coagulation.jpg
 * angiodysplasia of intestine
 * class of disease
 * intestinal disease angiodysplasia
 * Human disease
 * DOID:10846
 * angioid streaks
 * class of disease
 * retinal disease rare genetic eye disease genetic disease
 * Human disease
 * DOID:13401
 * C11.768.094
 * angioid streaks of choroid
 * class of disease
 * choroidal sclerosis angioid streaks nervous system heredodegenerative disease genetic vascular disease choroid disease retinal degeneration
 * angioid streaks that involves the optic choroid
 * DOID:979
 * angioimmunoblastic T-cell lymphoma
 * class of disease
 * T-cell lymphoma peripheral T-cell lymphoma immunoblastic lymphadenopathy
 * peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis
 * DOID:0111147
 * angiokeratoma
 * class of disease
 * skin hemangioma
 * benign cutaneous lesion of capillaries, resulting in small marks of red to blue color and characterized by hyperkeratosis
 * DOID:479
 * C04.557.645.115
 * Angiokeratoma
 * Angiokreatoma.jpg
 * angiokeratoma circumscriptum
 * class of disease
 * skin benign neoplasm angiokeratoma
 * Human disease
 * DOID:5949
 * angiokeratoma of Fordyce
 * class of disease
 * skin benign neoplasm angiokeratoma disease
 * sebaceous glands that are present in most individuals
 * DOID:664
 * Fordyce's spots
 * angiokeratoma of Mibelli
 * class of disease
 * angiokeratoma
 * Human disease
 * DOID:5948
 * angiolipoma
 * class of disease
 * lipoma
 * lipoma that is a painful subcutaneous nodule, having all other features of a typical lipoma
 * DOID:3616
 * C04.557.450.550.100
 * Angiolipoma
 * angioma serpiginosum
 * class of disease
 * skin hemangioma
 * skin hemangioma characterized by the presence of small red dots that cluster together to form a linear or snake-like array or ring-shaped pattern located in the blood vessels of the skin
 * DOID:4028
 * angiomatous meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:6548
 * angiomyolipoma
 * class of disease
 * benign neoplasms by histologic type disease
 * cell type benign neoplasm that from perivascular epithelioid cells
 * DOID:3314
 * C04.557.450.550.125 C04.557.450.692.249
 * Angiomyolipomas
 * angiomyoma
 * class of disease
 * benign perivascular tumor vascular disease
 * Human disease
 * DOID:4265
 * C04.557.450.590.450.125
 * angiosarcoma
 * class of disease
 * vascular tissue neoplasm vascular cancer disease
 * malignant Vascular tumor that results in rapidly proliferating, extensively infiltrating anaplastic cells derives from blood vessels and derived from the lining of irregular blood-filled spaces
 * DOID:0001816
 * Angiosarcoma
 * Angiosarcoma (5617087462).jpg
 * angle-closure glaucoma
 * class of disease
 * glaucoma
 * human disease
 * DOID:13550
 * C11.525.381.056
 * angular blepharoconjunctivitis
 * class of disease
 * blepharoconjunctivitis
 * blepharoconjunctivitis that is characterized by fissuring, scaling, maceration and erythema of the lateral or medial canthal area
 * DOID:2455
 * angular cheilitis
 * class of disease symptom or sign
 * cheilitis disease
 * cheilitis characterized by inflammation of one or both of the corners of the mouth
 * DOID:0060312
 * Angular cheilitis
 * Angular Cheilitis.JPG
 * anhidrosis
 * class of disease
 * hypohidrosis disease
 * Human disease
 * DOID:11156
 * animal phobia
 * class of disease
 * specific phobia disease
 * specific phobia that involves a fear caused by the presence or thought of a specific animal that poses little or no danger at all
 * DOID:600
 * aniseikonia
 * class of disease
 * refractive error dysmetropsia disease
 * Human disease
 * DOID:0050304 DOID:12274
 * C11.744.116
 * anismus
 * class of disease symptom or sign
 * focal dystonia constipation
 * failure of the normal relaxation of pelvic floor muscles during attempted defecation
 * DOID:0050839
 * anisometropia
 * class of disease
 * refractive error disease
 * human disease
 * DOID:12273
 * C11.744.126
 * ankyloglossia
 * class of disease
 * tongue disease genetic nervous system disorder genetic disease
 * congenital disorder of tongue mobility
 * DOID:0060604
 * C07.160
 * Ankyloglossia
 * Frenulum linguae.jpg
 * ankylosing spondylitis 1
 * class of disease
 * ankylosing spondylitis
 * human disease
 * DOID:0080603
 * ankylosing spondylitis 2
 * class of disease
 * ankylosing spondylitis autosomal dominant disease
 * human disease
 * DOID:0080604
 * ankylosing spondylitis 3
 * class of disease
 * ankylosing spondylitis
 * human disease
 * DOID:0080605
 * ankylosis
 * class of disease
 * arthropathy joint stiffness disease
 * Human disease
 * DOID:227
 * C05.550.069
 * Ankylosis
 * Annual and analytical cyclopaedia of practical medicine (1898) (14803296453).jpg
 * anodontia
 * class of disease
 * tooth agenesis tooth agenesis tooth abnormality tooth pathology disease
 * human disease
 * DOID:13714
 * C07.650.800.100 C07.793.700.100 C16.131.850.800.100
 * anomic aphasia
 * class of disease symptom or sign
 * aphasia clinical sign disease
 * type of aphasia
 * DOID:4541
 * C10.597.606.150.500.090 C23.888.592.604.150.500.090
 * anorexia nervosa
 * class of disease
 * eating disorder disease
 * type of eating disorder
 * DOID:8689
 * F03.400.128
 * Anorexia nervosa
 * Anorexia case 1900.jpg
 * anosognosia
 * class of disease
 * agnosia disease
 * Unawareness of one&#39;s own illness, symptoms or impairments
 * DOID:0060133
 * anovulation
 * class of disease
 * ovarian disease disease
 * human disease
 * DOID:3781
 * C13.351.500.056.630.050 C19.391.630.050 G08.686.784.690.080
 * anterior cerebral artery infarction
 * class of disease
 * cerebral infarction cerebral artery occlusion
 * Human disease
 * DOID:3528
 * C10.228.140.300.150.477.200.400 C10.228.140.300.510.200.325 C10.228.140.300.775.200.200.400 C14.907.253.092.477.200.400 C14.907.253.560.200.325 C14.907.253.855.200.200.400 C23.550.513.355.250.200.400 C23.550.717.489.250.200.400
 * anterior compartment syndrome
 * class of disease
 * compartment syndrome
 * disease
 * DOID:3933
 * C05.651.180.063 C14.907.303.063
 * anterior corneal pigmentation
 * class of disease
 * corneal deposit
 * Human disease
 * DOID:12307
 * anterior dislocation of lens
 * class of disease
 * globe disease lens subluxation
 * Human disease
 * DOID:2460
 * anterior horn cell disease
 * class of disease
 * spinal muscular atrophy
 * Human disease
 * DOID:4873
 * anterior ischemic optic neuropathy
 * class of disease
 * ischemic optic neuropathy optic nerve disease
 * Human disease
 * DOID:12010
 * anterior optic tract meningioma
 * class of disease
 * optic nerve tumor visual pathway meningioma
 * Human disease
 * DOID:6334
 * anterior scleritis
 * class of disease
 * scleritis
 * Human disease
 * DOID:13794
 * anterior segment dysgenesis 1
 * class of disease
 * corneal opacification and other ocular anomalies autosomal dominant disease
 * human disease
 * DOID:0080606
 * anterior segment dysgenesis 2
 * class of disease
 * autosomal recessive disease corneal opacification and other ocular anomalies
 * human disease
 * DOID:0080607
 * anterior segment dysgenesis 3
 * class of disease
 * autosomal dominant disease corneal opacification and other ocular anomalies
 * human disease
 * DOID:0080608
 * anterior segment dysgenesis 4
 * class of disease
 * corneal opacification and other ocular anomalies autosomal dominant disease
 * human disease
 * DOID:0080609
 * anterior segment dysgenesis 5
 * class of disease
 * corneal opacification and other ocular anomalies
 * human disease
 * DOID:0080610
 * anterior spinal artery syndrome
 * class of disease
 * syndrome cerebrovascular disease vascular myelopathy artery disease
 * Human disease
 * DOID:6712
 * C10.228.854.785.650.100 C14.907.790.550.100
 * anterior urethral cancer
 * class of disease
 * urethral cancer female urethral cancer
 * Human disease
 * DOID:8272
 * anterior uveitis
 * class of disease
 * uveitis panuveitis
 * Human disease
 * DOID:1407
 * C11.941.879.780.880
 * anterograde amnesia
 * class of disease
 * amnesia
 * loss of the ability to create new memories after the onset of amnesia
 * DOID:5340
 * C10.597.606.525.100.075 C23.888.592.604.529.100.075 F01.700.625.100.075 F03.615.200.137
 * anterolateral myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5845
 * anteroseptal myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5855
 * anthracosilicosis
 * class of disease
 * pneumoconiosis anthracosis
 * human disease
 * DOID:10324
 * C08.381.483.581.062.500 C08.381.483.581.760.125 C08.381.520.702.062.500 C08.381.520.702.760.125 C24.800.834.201
 * Coal workers pneumocniosis - Anthracosilicosis 1.jpg
 * anthracosis
 * class of disease
 * occupational disease pneumoconiosis disease
 * human disease
 * DOID:10327
 * C08.381.483.581.062 C08.381.520.702.062
 * Black lung disease
 * Anthracosis (4860889071).jpg
 * anti-basement membrane glomerulonephritis
 * class of disease
 * Goodpasture syndrome
 * Human disease
 * DOID:4780
 * antidepressant abuse
 * class of disease
 * substance abuse abuse of medicaments
 * substance abuse that involves the recurring use of antidepressant drugs despite negative consequences
 * DOID:11718
 * antisocial personality disorder
 * class of disease
 * Cluster B personality disorders personality disorder disease
 * Personality disorder that involves a pervasive pattern of disregard for other people
 * DOID:10939
 * F03.675.050
 * Antisocial personality disorder
 * antisynthetase syndrome
 * class of disease
 * autoimmune disease idiopathic inflammatory myopathy
 * human disease
 * DOID:0080744
 * anuria
 * class of disease symptom or sign
 * kidney disease oliguria urological symptom
 * lack of urine
 * DOID:2983
 * C12.050.351.968.419.078 C12.200.777.934.141 C12.200.777.419.078 C12.050.351.968.934.070 C12.950.419.078 C12.950.934.070
 * anus adenocarcinoma
 * class of disease
 * anal carcinoma adenocarcinoma
 * anal carcinoma that originating in the cortex of the adrenal gland and derives from epithelial cells of glandular origin
 * DOID:3447
 * anus basaloid carcinoma
 * class of disease
 * anal squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7174
 * anus leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of anus rectum leiomyoma anus neoplasm
 * Human disease
 * DOID:5134
 * anus leiomyosarcoma
 * class of disease
 * anus sarcoma leiomyosarcoma rectum leiomyosarcoma
 * human disease
 * DOID:5267
 * anus lymphoma
 * class of disease
 * anal cancer lymphoma
 * Human disease
 * DOID:14139
 * anus neoplasm
 * class of disease
 * intestinal neoplasm anal disease intestinal benign neoplasm
 * Human disease
 * DOID:4551
 * C04.588.274.476.411.307.790.040 C06.301.371.411.307.790.040 C06.405.249.411.307.790.040 C06.405.469.491.307.790.040 C06.405.469.860.101.163 C06.405.469.860.180.500.040
 * anus rhabdomyosarcoma
 * class of disease
 * anus sarcoma rhabdomyosarcoma rectum rhabdomyosarcoma anal cancer
 * rhabdomyosarcoma and sarcoma of the anus that is located in the anus
 * DOID:4066
 * anus sarcoma
 * class of disease
 * anal cancer sarcoma intestinal benign neoplasm
 * sarcoma and malignant neoplasm of anus that is located in the anus
 * DOID:4067
 * anxiety disorder
 * class of disease
 * cognitive disorder disease
 * cognitive disorder with an excessive, irrational dread of everyday situations
 * DOID:2030
 * F03.080
 * Anxiety disorders
 * aorta angiosarcoma
 * class of disease
 * angiosarcoma aortic disease
 * human disease
 * DOID:4510
 * aorta atresia
 * class of disease
 * aortic disease
 * aortic disease that is characterized by an absence of an opening from the left ventricle of the heart into the aorta
 * DOID:14037
 * aortic aneurysm
 * class of disease
 * aortic disease aneurysm clinical sign disease
 * aorta to greater than 1.5 times normal size
 * DOID:3627
 * C14.907.055.239 C14.907.109.139
 * Aortic aneurysms
 * aortic atherosclerosis
 * class of disease
 * atherosclerosis
 * Human disease
 * DOID:10230
 * aortic disease
 * class of disease
 * artery disease
 * artery disease characterized by degeneration of the cells composing the aortic wall
 * DOID:520
 * C14.907.109
 * aortic malignant tumor
 * class of disease
 * vascular cancer aortic disease
 * Human disease
 * DOID:8352
 * aortic valve disease
 * class of disease
 * heart valve disease aortic disease
 * Human disease
 * DOID:62
 * C14.280.484.048
 * Aortic valve diseases
 * aortic valve disease 1
 * class of disease
 * familial bicuspid aortic valve
 * bicuspid aortic valve disease that has material basis in heterozygous mutation in the NOTCH1 gene on chromosome 9q34
 * DOID:0080333
 * aortic valve disease 2
 * class of disease
 * familial bicuspid aortic valve autosomal dominant disease
 * bicuspid aortic valve disease that has material basis in heterozygous mutation in the SMAD6 gene on chromosome 15q22
 * DOID:0080334
 * aortic valve insufficiency
 * class of disease
 * aortic valve disease valve insufficiency disease
 * aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle
 * DOID:57
 * C14.280.484.095
 * Aortic valve insufficiency
 * Myxomatous aortic valve.jpg
 * aortic valve prolapse
 * class of disease
 * aortic valve disease heart valve prolapse
 * Human disease
 * DOID:5232
 * C14.280.484.400.100
 * aortitis
 * class of disease
 * aortic disease
 * inflammation of the aortic wall
 * DOID:519
 * C14.907.109.320 C14.907.940.080
 * Aortitis
 * aphasia
 * class of disease symptom or sign
 * language disorder neurological symptom specific language impairment-5 disease
 * Inability to spoke
 * DOID:0060046
 * C10.597.606.150.500.800.100 C23.888.592.604.150.500.800.100
 * Aphasia
 * aphthous stomatitis
 * class of disease symptom or sign
 * clinical sign stomatitis lesions in mouth disease
 * stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers
 * DOID:9663
 * C07.465.864.750
 * Aphthous ulcer
 * Aphthe Unterlippe.jpg
 * apical granuloma
 * class of disease
 * disease periapical periodontitis granuloma
 * tooth disease
 * DOID:4617
 * C07.320.830.700.740 C07.465.714.306.700.740 C07.465.714.533.487.740
 * apical myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5848
 * apocrine adenocarcinoma
 * class of disease
 * apocrine sweat gland cancer sweat gland carcinoma adenocarcinoma Apocrine gland carcinoma
 * apocrine sweat gland cancer that derives from epithelial cells of glandular origin
 * DOID:4933
 * apocrine adenoma
 * class of disease
 * apocrine sweat gland neoplasm
 * Human disease
 * DOID:3895
 * apocrine adenosis of breast
 * class of disease
 * non-proliferative fibrocystic change of the breast
 * Human disease
 * DOID:5999
 * apocrine sweat gland cancer
 * class of disease
 * sweat gland cancer apocrine sweat gland neoplasm
 * Human disease
 * DOID:4934
 * apocrine sweat gland neoplasm
 * class of disease
 * sweat gland neoplasm apocrine sweat gland disease
 * Human disease
 * DOID:5876
 * apolipoprotein C-3 deficiency
 * class of disease
 * cholesterol-ester transfer protein deficiency autosomal dominant disease
 * human disease
 * DOID:0111370
 * appendiceal neoplasm
 * class of disease
 * intestinal neoplasm appendix disease cecal neoplasm intestinal benign neoplasm
 * Human disease
 * DOID:11240
 * C04.588.274.476.411.184.290 C06.301.371.411.184.290 C06.405.249.411.184.290 C06.405.469.110.417.290 C06.405.469.491.184.290
 * Appendiceal neoplasms
 * appendix cancer
 * class of disease
 * intestinal cancer appendiceal neoplasm appendix disease
 * cancer that is located in the appendix
 * DOID:11239
 * Appendiceal cancer
 * appendix disease
 * class of disease
 * gastrointestinal system disease cecal disease
 * gastrointestinal system disease that is located in the appendix
 * DOID:60000
 * Diseases and disorders of appendix
 * appendix lymphoma
 * class of disease
 * appendix cancer primary organ-specific lymphoma
 * human disease
 * DOID:11241
 * apperceptive agnosia
 * class of disease
 * visual agnosia agnosia
 * agnosia that is a loss of the ability to distinguish visual shapes
 * DOID:0060134
 * apple allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Malus domestica plant fruit food product.
 * DOID:0060504
 * apricot allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus armeniaca plant fruit food product.
 * DOID:0060505
 * aqueous misdirection
 * class of disease
 * glaucoma
 * Human disease
 * DOID:11149
 * arcus senilis
 * class of disease
 * corneal degeneration rare genetic eye disease genetic disease disease
 * Human disease
 * DOID:11342
 * C11.204.299.070
 * Arcus senilis
 * Four representative slides of corneal arcus.jpg
 * ariboflavinosis
 * class of disease
 * nutritional deficiency disease vitamin deficiency vitamin B deficiency disease
 * Human disease
 * DOID:8454
 * C18.654.521.500.133.699.713
 * Angular Cheilitis.JPG
 * arrhythmogenic right ventricular dysplasia 1
 * class of disease
 * arrhythmogenic right ventricular cardiomyopathy autosomal dominant disease
 * arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the TGFB3 gene on chromosome 14q24
 * DOID:0110070
 * arrhythmogenic right ventricular dysplasia 3
 * class of disease
 * arrhythmogenic right ventricular cardiomyopathy autosomal dominant disease
 * arrhythmogenic right ventricular dysplasia associated with variation in the region 14q12-q22
 * DOID:0110072
 * arrhythmogenic right ventricular dysplasia 4
 * class of disease
 * arrhythmogenic right ventricular cardiomyopathy autosomal dominant disease
 * An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.
 * DOID:0110073
 * arrhythmogenic right ventricular dysplasia 6
 * class of disease
 * arrhythmogenic right ventricular cardiomyopathy
 * arrhythmogenic right ventricular dysplasia associated with variation in the region 10p14-p12
 * DOID:0110075
 * arterial hypertension
 * class of disease symptom or sign
 * vascular disease artery disease clinical sign hypertension disease
 * long term medical condition with elevated arterial blood pressure
 * DOID:10763
 * C14.907.489
 * Hypertension
 * Grade 1 hypertension.jpg
 * arteriolosclerosis
 * class of disease
 * arteriosclerosis coronary artery disease
 * Human disease
 * DOID:5162
 * C14.907.137.126.056
 * Arteriolosclerosis
 * arteriosclerosis
 * class of disease
 * artery disease disease
 * thickening, hardening and loss of elasticity of the walls of arteries
 * DOID:2349
 * C14.907.137.126
 * Atherosclerosis
 * Atherosclerosis, aorta, gross pathology PHIL 846 lores.jpg
 * arteriosclerosis obliterans
 * class of disease
 * arteriosclerosis peripheral artery disease coronary artery disease
 * human disease
 * DOID:5160
 * C14.907.137.126.114
 * arteriosclerotic cardiovascular disease
 * class of disease
 * arteriosclerosis coronary artery disease
 * human disease
 * DOID:2348
 * arteritic anterior ischemic optic neuropathy
 * class of disease
 * anterior ischemic optic neuropathy
 * Human disease
 * DOID:0050863
 * artery disease
 * class of disease
 * vascular disease
 * type of vascular disease
 * DOID:0050828
 * arthrogryposis multiplex congenita-4
 * class of disease
 * autosomal recessive disease
 * human disease
 * DOID:0080980
 * arthrogryposis, renal dysfunction, and cholestasis 1
 * class of disease
 * arthrogryposis–renal dysfunction–cholestasis syndrome
 * human disease
 * DOID:0111353
 * arthrogryposis, renal dysfunction, and cholestasis 2
 * class of disease
 * arthrogryposis–renal dysfunction–cholestasis syndrome
 * human disease
 * DOID:0111354
 * arthropathy
 * class of disease
 * joint disorder bone disease disease
 * disease of a joint
 * DOID:381
 * C05.550
 * Arthropathies
 * arthus reaction
 * class of disease
 * type III hypersensitivity
 * Human disease
 * DOID:1556
 * C20.543.520.100
 * articulation disorder
 * class of disease
 * speech disorder language disorder
 * speech disorder that involves mispronouncing speech sounds by omitting, distorting, substituting, or adding sounds which can make speech difficult to understand
 * DOID:4186
 * C10.597.606.150.500.800.150 C23.888.592.604.150.500.800.150
 * asbestos-related lung carcinoma
 * class of disease
 * lung carcinoma
 * Human disease
 * DOID:7596
 * asbestosis
 * class of disease
 * pneumoconiosis asbestos-related disease disease
 * pneumoconiosis caused by inhalation and retention of asbestos fibers
 * DOID:10320
 * C08.381.483.581.125 C08.381.520.702.125 C24.800.127
 * Asbestosis
 * Early Asbestosis in a Retired Pipe Fitter.jpg
 * ascending cholangitis
 * class of disease symptom or sign
 * non-neoplastic bile duct disorder inflammatory disease bile duct disease disease
 * bile duct disease that is an inflammation of the bile duct
 * DOID:9446
 * C06.130.120.200
 * Ascending cholangitis
 * Cholangitis.jpg
 * ascending cholangitis
 * class of disease
 * ascending cholangitis
 * Human disease
 * DOID:14270
 * ascending colon cancer
 * class of disease
 * plump cancer
 * Human disease
 * DOID:218
 * aseptic meningitis
 * class of disease
 * meningitis non-infectious meningitis disease
 * meningitis caused by anything other than bacteria
 * DOID:12157
 * C10.586.625.220
 * aspergillosis
 * class of disease
 * opportunistic mycosis disease
 * infectious disease of humans, birds and other animals
 * DOID:13564
 * C01.150.703.080
 * Aspergillosis
 * Pulmonary aspergillosis (1) invasive type.jpg
 * asphyxia neonatorum
 * class of disease
 * respiratory disease perinatal respiratory disorder disease
 * Respiratory failure in the newborn. (Dorland, 27th ed)
 * DOID:11088
 * C16.614.092
 * asphyxiating thoracic dysplasia
 * class of disease
 * osteochondrodysplasia autosomal recessive disease bone development disease
 * human disease
 * DOID:0050592
 * Asphyxiating thoracic dysplasia
 * asphyxiating thoracic dystrophy 1
 * class of disease
 * asphyxiating thoracic dysplasia autosomal recessive disease
 * asphyxiating thoracic dystrophy associated with variation in the region 15q13
 * DOID:0110085
 * aspiration pneumonia
 * class of disease symptom or sign
 * bacterial pneumonia disease
 * bronchopneumonia that develops due to the entrance of foreign materials into the lungs
 * DOID:0050152
 * C08.381.677.529 C08.730.610.529
 * Aspiration pneumonia
 * Aspiration pneumonia (4861515094).jpg
 * aspiration pneumonitis
 * class of disease
 * pneumonia aspiration pneumonia disease
 * chemical pneumonitis or aspiration pneumonitis caused by aspiration during anaesthesia, especially during pregnancy
 * DOID:3240
 * aspirin-induced respiratory disease
 * class of disease
 * intrinsic asthma salicylate sensitivity
 * human disease
 * DOID:0080822
 * associative agnosia
 * class of disease
 * visual agnosia agnosia
 * agnosia that is a loss of the ability to recognize visual scenes or classes of objects but retain the abilty to describe them
 * DOID:0060136
 * astereognosia
 * class of disease
 * agnosia tactile agnosia
 * agnosia that is the loss of the ability to recognize objects by touch based on its texture, size and weight
 * DOID:0060150
 * asthma
 * class of disease
 * bronchospasm disease
 * long-term disease involving inflamed airways
 * DOID:2841
 * C08.127.108 C08.381.495.108 C08.674.095 C20.543.480.680.095
 * Asthma
 * Asthma.jpg
 * astigmatism
 * class of disease symptom or sign
 * refractive error disease astigmatism
 * refractive error characterized by the optics of the eye to focus a point object into a sharp focused image on the retina, has_symptom blurred vision.
 * DOID:11782
 * C11.744.212
 * Astigmatism (eye)
 * Astigmatism.jpg
 * astroblastoma
 * class of disease
 * astrocytoma
 * glial tumor derived from the astroblast, a type of cell that closely resembles spongioblastoma and astrocytes
 * DOID:7305
 * Astroblastoma
 * astrocytoma
 * class of disease
 * glioma cerebrum cancer central nervous system cancer disease
 * type of cancer of the brain originating in a particular kind of glial cells, star-shaped brain cells in the cerebrum called astrocytes
 * DOID:3069
 * C04.557.465.625.600.380.080 C04.557.470.670.380.080 C04.557.580.625.600.380.080
 * Astrocytic tumors
 * Astrocytoma.jpg
 * asymmetric motor neuropathy
 * class of disease
 * motor neuritis
 * Human disease
 * DOID:7559
 * asymptomatic dengue
 * class of disease
 * dengue fever asymptomatic disease
 * A dengue disease that results in infection, has material basis in Dengue virus [NCBITaxon:12637] with four serotypes (Dengue virus 1, 2, 3 and 4), which are transmitted by Aedes mosquito bite. The infection has no manifestations of symptoms.
 * DOID:0050143
 * asymptomatic neurosyphilis
 * class of disease
 * tertiary neurosyphilis
 * tertiary neurosyphilis that results in mild meningitis
 * DOID:10035
 * asynchronous multifocal osteogenic sarcoma
 * class of disease
 * multifocal osteogenic sarcoma
 * Human disease
 * DOID:6697
 * ataxia and polyneuropathy, adult-onset
 * class of disease
 * genetic disease mitochondrial disease
 * human disease
 * DOID:0111750
 * ataxia with oculomotor apraxia type 3
 * class of disease
 * autosomal recessive cerebellar ataxia oculomotor apraxia spinocerebellar ataxia with axonal neuropathy type 2
 * human disease
 * DOID:0060557
 * ataxic cerebral palsy
 * class of disease
 * cerebral palsy
 * A cerebral palsy that is caused by damage to the cerebellum, which affects muscle coordination, particularly in the limb. Some individuals suffer from hypotonia, tremors, difficulty with visual and/or auditory processing.
 * DOID:0050670
 * atheroembolism of kidney
 * class of disease
 * cholesterol embolism kidney disease
 * Human disease
 * DOID:1460
 * atherosclerosis
 * class of disease
 * arteriosclerotic cardiovascular disease arteriosclerosis disease
 * human disease
 * DOID:1936
 * C14.907.137.126.307
 * Atherosclerosis
 * Endothelial dysfunction Atherosclerosis.png
 * atopic dermatitis
 * class of disease symptom or sign
 * dermatitis allergic contact dermatitis disease
 * type of inflammation of the skin
 * DOID:3310
 * C16.320.850.210 C17.800.174.193 C17.800.815.193 C17.800.827.210 C20.543.480.343
 * Atopic dermatitis
 * Atopic dermatitis.png
 * atopic dermatitis 2
 * class of disease
 * atopic dermatitis
 * atopic dermatitis conferred by variation in the FLG gene on chromosome 1q21
 * DOID:0110098
 * atopic dermatitis 3
 * class of disease
 * atopic dermatitis
 * atopic dermatitis associated with variation in the region 20p
 * DOID:0110099
 * atopic dermatitis 4
 * class of disease
 * atopic dermatitis
 * An atopic dermatitis associated with variation in the region 17q25.3.
 * DOID:0110100
 * atopic dermatitis 5
 * class of disease
 * atopic dermatitis
 * atopic dermatitis associated with variation in the region 13q12-q14
 * DOID:0110101
 * atopic dermatitis 6
 * class of disease
 * atopic dermatitis
 * atopic dermatitis associated with variation in the region 5q31-q33
 * DOID:0110102
 * atopic dermatitis 7
 * class of disease
 * atopic dermatitis
 * An atopic dermatitis associated with variation in the region 11q13.5.
 * DOID:0110103
 * atopic dermatitis 8
 * class of disease
 * atopic dermatitis
 * An atopic dermatitis associated with variation in the region 4q22.1.
 * DOID:0110104
 * atopic dermatitis 9
 * class of disease
 * atopic dermatitis
 * atopic dermatitis associated with variation in the region 3p24
 * DOID:0110105
 * atrial heart septal defect 1
 * class of disease
 * atrial heart septal defect
 * atrial heart septal defect type 1 associated with variation in the region 5p
 * DOID:0110106
 * atrophic gastritis
 * class of disease
 * gastritis chronic gastritis
 * Human disease
 * DOID:8929
 * C06.405.205.697.394 C06.405.748.398.394
 * Atrophic gastritis
 * atrophic muscular disease
 * class of disease
 * neuromuscular disease muscle tissue disease muscular disease
 * neuromuscular disease characterized by an abnormal reduction in the muscle volume and atrophy
 * DOID:913
 * C05.651.534 C10.668.491.175
 * atrophic nonflaccid tympanic membrane
 * class of disease
 * tympanic membrane disease Tympanic membrane retraction
 * Human disease
 * DOID:12546
 * atrophic vaginitis
 * class of disease
 * vaginitis disease
 * inflammation of the vagina due to the thinning and shrinking of the tissues, as well as decreased lubrication
 * DOID:11968
 * C13.351.500.894.906.316
 * Atrophic vaginitis
 * atrophic vulva
 * class of disease
 * vulvar disease
 * Human disease
 * DOID:14275
 * atrophodermia vermiculata
 * class of disease
 * keratosis pilaris atropicans
 * Dermatological condition
 * DOID:0080756
 * atrophy of prostate
 * class of disease
 * prostate disease
 * Human disease
 * DOID:2301
 * atypical Gaucher's disease due to saposin c deficiency
 * class of disease
 * Gaucher's disease genetic disease
 * A Gaucher&#39;s disease that has material basis in an autosomal recessive mutation of PSAP on chromosome 10q22.1.
 * DOID:0110961
 * atypical autism
 * class of disease
 * autism spectrum disorder pervasive developmental disorder disease
 * autism spectrum disorder that involves some autistic symptoms occuring after age 3 with an abscence of all the traits necessary for a diagnosis of autism
 * DOID:0060042
 * atypical breast papilloma
 * class of disease
 * breast duct papilloma
 * Human disease
 * DOID:8227
 * atypical choroid plexus papilloma
 * class of disease
 * choroid plexus neoplasm papilloma cerebrovascular benign neoplasm
 * Human disease
 * DOID:3544
 * atypical chronic myeloid leukemia
 * class of disease
 * myelodysplastic/myeloproliferative neoplasm chronic myeloid leukemia
 * A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene.
 * DOID:0060597
 * C04.557.337.539.300 C15.378.190.615.500
 * atypical depressive disorder
 * class of disease
 * mood disorder disease
 * depression characterized by improved mood in response to positive events
 * DOID:12294
 * Atypical depression
 * atypical follicular adenoma
 * class of disease
 * follicular adenoma
 * Human disease
 * DOID:8292
 * atypical hereditary sensory neuropathy
 * class of disease
 * hereditary sensory and autonomic neuropathy
 * hereditary sensory neuropathy characterized by late onset of sensory ataxia without ulcerating acropathy or autonomic abnormalities
 * DOID:0070160
 * atypical lipomatous tumor
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5690
 * atypical neurofibroma
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:5153
 * atypical polypoid adenomyoma
 * class of disease
 * adenomyoma
 * Human disease
 * DOID:4993
 * auditory agnosia
 * class of disease
 * agnosia music-specific disorders
 * agnosia that is a loss of the ability to distinguishing environmental and non-verbal auditory cues including difficulty distinguishing speech from non-speech sounds even though hearing is usually normal
 * DOID:0060137
 * auricular cancer
 * class of disease
 * ear neoplasms
 * human disease
 * DOID:5101
 * autoimmune atherosclerosis
 * class of disease
 * autoimmune disease of cardiovascular system
 * autoimmune disease of cardiovascular system that is characterized by a build up of plaque in the arteries
 * DOID:0040096
 * autoimmune cardiomyopathy
 * class of disease
 * autoimmune disease of cardiovascular system heart disease immune disorder cardiomyopathy
 * autoimmune disease of cardiovascular system that is characterized by deterioration of the function of the heart muscle
 * DOID:0040095
 * autoimmune cholangitis
 * class of disease
 * autoimmune hepatitis ascending cholangitis
 * human disease
 * DOID:0080742
 * autoimmune disease
 * class of disease
 * hypersensitivity disease immune disorder primary immunodeficiency disease
 * type of human disease
 * DOID:417
 * C20.111
 * Autoimmune diseases and disorders
 * Warm autoimmune hemolytic anemia.jpg
 * autoimmune disease of blood
 * class of disease
 * autoimmune disease
 * hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the blood
 * DOID:0060050
 * autoimmune disease of cardiovascular system
 * class of disease
 * autoimmune disease cardiovascular disease
 * hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the cardiovascular system.
 * DOID:0060051
 * autoimmune disease of central nervous system
 * class of disease
 * autoimmune disease of the nervous system central nervous system disease
 * autoimmune disease of the central nervous system
 * DOID:0060004
 * autoimmune disease of endocrine system
 * class of disease
 * autoimmune disease endocrine system disease
 * hypersensitivity reaction type II disease that is the abnormal functioning of the immune system resulting in production of antibodies or T cells against cells and/or tissues in the endocrine system
 * DOID:0060005
 * autoimmune disease of exocrine system
 * class of disease
 * autoimmune disease
 * immune system disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the exocrine system
 * DOID:0060029
 * autoimmune disease of eyes, ear, nose and throat
 * class of disease
 * autoimmune disease of the nervous system sensory system disease
 * hypersensitivity reaction type II disease of the eyes, ears, nose and throat
 * DOID:0060030
 * autoimmune disease of gastrointestinal tract
 * class of disease
 * autoimmune disease gastrointestinal system disease
 * hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the gastrointestinal tract
 * DOID:0060031
 * autoimmune disease of musculoskeletal system
 * class of disease
 * autoimmune disease musculoskeletal disorder
 * autoimmune disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the musculoskeletal system
 * DOID:0060032
 * autoimmune disease of peripheral nervous system
 * class of disease
 * autoimmune disease of the nervous system peripheral neuropathy
 * autoimmune disease of the nervous system that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the peripheral nervous system
 * DOID:0060033
 * autoimmune disease of the nervous system
 * class of disease
 * autoimmune disease nervous system disease neurological disorder
 * A disorder characterized by the degeneration of the nervous system due to autoimmunity. Representative examples include multiple sclerosis, Guillain-Barre syndrome, and myasthenia gravis.
 * DOID:438
 * C10.114 C20.111.258
 * autoimmune disease of urogenital tract
 * class of disease
 * autoimmune disease reproductive system disease urinary system disease
 * hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the urogenital tract
 * DOID:0060049
 * autoimmune gastritis
 * class of disease
 * autoimmune disease of gastrointestinal tract stomach disease gastritis
 * autoimmune disease of gastrointestinal tract that is located in the stomach
 * DOID:0040090
 * autoimmune glomerulonephritis
 * class of disease
 * autoimmune disease of urogenital tract immune disorder rare urogenital disease glomerulonephritis
 * human disease
 * DOID:0040094
 * autoimmune myocarditis
 * class of disease
 * autoimmune cardiomyopathy myocarditis autoimmune disease of cardiovascular system
 * DOID:0080767
 * autoimmune neuropathy
 * class of disease
 * autoimmune disease of central nervous system
 * autoimmune disease of centreal nervous system caused by an autoimmune response
 * DOID:0060499
 * autoimmune optic neuritis
 * class of disease
 * autoimmune disease of peripheral nervous system optic neuritis
 * autoimmune disease of peripheral nervous system that is located in the neuron projection bundle connecting eye with brain
 * DOID:0040089
 * autoimmune pancreatitis
 * class of disease
 * chronic pancreatitis IgG4-related disease autoimmune disease of endocrine system pancreas disease
 * type of chronic pancreatitis
 * DOID:0040091
 * C06.689.750.830.500 C20.111.296 C23.550.291.500.750.500
 * autoimmune peripheral neuropathy
 * class of disease
 * autoimmune disease of peripheral nervous system
 * autoimmune disease of peripheral nervous system that results in peripheral neuropathy
 * DOID:0040087
 * autoimmune polyendocrine syndrome
 * class of disease
 * autoimmune disease of endocrine system polyglandular dysfunction disease
 * autoimmune disease of endocrine system with auto-reactivity against endocrine organs
 * DOID:14040
 * C19.787 C20.111.750
 * autoimmune polyendocrine syndrome type 2
 * class of disease
 * autoimmune polyendocrine syndrome
 * An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene.
 * DOID:0050168
 * autoimmune skin disease
 * class of disease
 * autoimmune disease skin disease rheumatic disease cellulitis rare skin disease immune disorder autoimmune disease of musculoskeletal system connective tissue disease
 * hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the skin and connective tissue
 * DOID:0060039
 * autoimmune thyroiditis
 * class of disease
 * autoimmune disease of endocrine system thyroiditis disease
 * autoimmune disease of endocrine system that involves inflammation located in thyroid gland caused by the immune system reacting against its own tissues
 * DOID:7188
 * C19.874.871.102 C20.111.809
 * autoimmune vasculitis
 * class of disease
 * autoimmune disease of cardiovascular system immune disorder vasculitis
 * autoimmune disease of cardiovascular system that is characterized by inflammation of the blood vessels
 * DOID:0040097
 * autonomic nervous system benign neoplasm
 * class of disease
 * peripheral nervous system benign neoplasm autonomic nervous system neoplasm
 * human disease
 * DOID:0080321
 * autonomic nervous system disease
 * class of disease
 * peripheral neuropathy
 * human disease
 * DOID:11465
 * Diseases and disorders of autonomic nervous system
 * autonomic nervous system neoplasm
 * class of disease
 * peripheral nervous system neoplasm autonomic nervous system disease
 * peripheral nervous system neoplasm that is located in the autonomic nervous system
 * DOID:2621
 * autonomic neuropathy
 * class of disease
 * autonomic nervous system disease polyneuropathy
 * human disease
 * DOID:11504
 * autonomic peripheral neuropathy
 * class of disease
 * peripheral neuropathy autonomic neuropathy
 * Human disease
 * DOID:0060054
 * autosomal dominant Aarskog syndrome
 * class of disease
 * Aarskog syndrome autosomal dominant disease
 * human disease
 * DOID:0111825
 * autosomal dominant Emery-Dreifuss muscular dystrophy 2
 * class of disease
 * Emery-Dreifuss muscular dystrophy autosomal dominant disease
 * Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of LMNA on chromosome 1q22
 * DOID:0070247
 * autosomal dominant Emery-Dreifuss muscular dystrophy 4
 * class of disease
 * Emery-Dreifuss muscular dystrophy autosomal dominant disease
 * An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of SYNE1 on chromosome 6q25.2.
 * DOID:0070249
 * autosomal dominant Emery-Dreifuss muscular dystrophy 5
 * class of disease
 * Emery-Dreifuss muscular dystrophy autosomal dominant disease
 * An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of SYNE2 on chromosome 14q23.2.
 * DOID:0070250
 * autosomal dominant Emery-Dreifuss muscular dystrophy 7
 * class of disease
 * Emery-Dreifuss muscular dystrophy autosomal dominant disease
 * An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of TMEM43 on chromosome 3p25.1.
 * DOID:0070252
 * autosomal dominant Kenny-Caffey syndrome
 * class of disease
 * Kenny-Caffey syndrome autosomal dominant disease
 * human disease
 * DOID:0080723
 * autosomal dominant Parkinson disease 1
 * class of disease
 * hereditary late onset Parkinson disease autosomal dominant disease
 * human disease
 * DOID:0060367
 * autosomal dominant Parkinson's disease 22
 * class of disease
 * autosomal dominant disease hereditary late onset Parkinson disease
 * A late onset Parkinson&#39;s disease that has material basis in heterozygous mutation in the CHCHD2 gene on chromosome 7p11.2
 * DOID:0080504
 * autosomal dominant Wolfram syndrome
 * class of disease
 * Wolfram syndrome autosomal dominant disease
 * Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has material basis in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16
 * DOID:0080584
 * autosomal dominant centronuclear myopathy
 * class of disease
 * centronuclear myopathy
 * centronuclear myopathy that has material basis in autosomal dominant inheritance
 * DOID:0111217
 * autosomal dominant chondrodysplasia punctata
 * class of disease
 * chondrodysplasia punctata autosomal dominant disease
 * Human disease
 * DOID:0060293
 * autosomal dominant craniodiaphyseal dysplasia
 * class of disease
 * autosomal dominant disease craniodiaphyseal dysplasia
 * human disease
 * DOID:0080807
 * autosomal dominant craniometaphyseal dysplasia
 * class of disease
 * autosomal dominant disease craniometaphyseal dysplasia
 * human disease
 * DOID:0080801
 * autosomal dominant cutis laxa
 * class of disease
 * cutis laxa autosomal dominant disease
 * cutis laxa characterized by autosomal dominant inheritance of skin that is loose, hanging, wrinkled and lacking in elasticity
 * DOID:0070142
 * autosomal dominant cutis laxa 1
 * class of disease
 * autosomal dominant cutis laxa
 * autosomal dominant cutis laxa that has material basis in heterozygous mutations in the ELN gene on chromosome 7q11
 * DOID:0070130
 * autosomal dominant cutis laxa 2
 * class of disease
 * autosomal dominant cutis laxa
 * autosomal dominant cutis laxa that has material basis in heterozygous mutation in the FBLN5 gene on chromosome 14q32
 * DOID:0070136
 * autosomal dominant disease
 * class of disease
 * autosomal genetic disease
 * genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease
 * DOID:0050736
 * autosomal dominant distal hereditary motor neuropathy
 * class of disease
 * Distal hereditary motor neuropathies spinal muscular atrophy autosomal dominant disease
 * Autosomal dominant form of distal hereditary motor neuropathy
 * DOID:0111198
 * autosomal dominant dyskeratosis congenita 1
 * class of disease
 * dyskeratosis congenita autosomal dominant disease
 * A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERC on chromosome 3q26.2.
 * DOID:0070014
 * autosomal dominant dyskeratosis congenita 2
 * class of disease
 * dyskeratosis congenita autosomal dominant disease
 * A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERT on chromosome 5p15.33.
 * DOID:0070016
 * autosomal dominant dyskeratosis congenita 3
 * class of disease
 * dyskeratosis congenita autosomal dominant disease
 * dyskeratosis congenita that has material basis in an autosomal dominant mutation of TINF2 on chromosome 14q12
 * DOID:0070018
 * autosomal dominant dyskeratosis congenita 4
 * class of disease
 * dyskeratosis congenita autosomal dominant disease
 * A dyskeratosis congenita that has material basis in an autosomal dominant mutation of RTEL1 on chromosome 20q13.33.
 * DOID:0070020
 * autosomal dominant dyskeratosis congenita 6
 * class of disease
 * dyskeratosis congenita autosomal dominant disease
 * A dyskeratosis congenita that has material basis in an autosomal dominant mutation of ACD on chromosome 16q22.1.
 * DOID:0070023
 * autosomal dominant hyaline body myopathy
 * class of disease
 * hyaline body myopathy autosomal dominant disease
 * A hyaline body myopathy that has material basis in heterozygous mutation in MYH7 on 14q11.2.
 * DOID:0111269
 * autosomal dominant hypocalcemia
 * class of disease
 * hypocalcaemia autosomal dominant disease metal metabolism disorder
 * calcium metabolism disease characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone
 * DOID:0090109
 * autosomal dominant keratitis-ichthyosis-deafness syndrome
 * class of disease
 * autosomal dominant disease keratitis–ichthyosis–deafness syndrome syndrome
 * autosomal dominant disease characterized by congenital deafness, keratopachydermia and constrictions of fingers and toes that has material basis in heterozygous mutation in the GJB2 gene on chromosome 13q
 * DOID:0060871
 * autosomal dominant limb-girdle muscular dystrophy type 1
 * class of disease
 * autosomal dominant limb-girdle muscular dystrophy
 * autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the DNAJB6 gene on chromosome 7q36
 * DOID:0110305
 * autosomal dominant limb-girdle muscular dystrophy type 1H
 * class of disease
 * autosomal dominant limb-girdle muscular dystrophy
 * An autosomal dominant limb-girdle muscular dystrophy that has material basis in with variation in the region 3p25.1-p23.
 * DOID:0110303
 * autosomal dominant mental retardation 45
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080236
 * autosomal dominant mental retardation 46
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080237
 * autosomal dominant mental retardation 47
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080238
 * autosomal dominant mental retardation 48
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080235
 * autosomal dominant mental retardation 49
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080234
 * autosomal dominant mental retardation 50
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080233
 * autosomal dominant mental retardation 51
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080232
 * autosomal dominant mental retardation 52
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080231
 * autosomal dominant mental retardation 53
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080228
 * autosomal dominant mental retardation 54
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * human disease
 * DOID:0080230
 * autosomal dominant mental retardation 55
 * class of disease
 * autosomal dominant disease syndromic intellectual disability
 * human disease
 * DOID:0080227
 * autosomal dominant mental retardation 56
 * class of disease
 * autosomal dominant disease syndromic intellectual disability
 * human disease
 * DOID:0080226
 * autosomal dominant microcephaly
 * class of disease
 * autosomal dominant disease microcephaly
 * human disease
 * DOID:14725
 * autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques
 * class of disease
 * autosomal dominant disease Olmsted syndrome
 * human disease
 * DOID:0112013
 * autosomal dominant nocturnal frontal lobe epilepsy 1
 * class of disease
 * autosomal dominant nocturnal frontal lobe epilepsy
 * autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the CHRNA4 gene on chromosome 20q13
 * DOID:0060682
 * autosomal dominant nocturnal frontal lobe epilepsy 2
 * class of disease
 * autosomal dominant nocturnal frontal lobe epilepsy
 * autosomal dominant nocturnal frontal lobe epilepsy that has material basis in variation in the chromosome region 15q24
 * DOID:0060683
 * autosomal dominant nocturnal frontal lobe epilepsy 5
 * class of disease
 * autosomal dominant nocturnal frontal lobe epilepsy
 * autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34
 * DOID:0060686
 * autosomal dominant non-syndromic intellectual disability 1
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MBD5 on chromosome 2q23.1.
 * DOID:0070031
 * autosomal dominant non-syndromic intellectual disability 2
 * class of disease
 * autosomal dominant non-syndromic intellectual disability
 * autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DOCK8 on chromosome 9p24
 * DOID:0070032
 * autosomal dominant nonsyndromic deafness 1
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has material basis in mutation in the DIAPH1 gene on chromosome 5q31
 * DOID:0110541
 * autosomal dominant nonsyndromic deafness 18
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22
 * DOID:0110549
 * autosomal dominant nonsyndromic deafness 30
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 15q25-q26
 * DOID:0110560
 * autosomal dominant nonsyndromic deafness 33
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 13q34
 * DOID:0110562
 * autosomal dominant nonsyndromic deafness 47
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 9p22-p21
 * DOID:0110570
 * autosomal dominant nonsyndromic deafness 52
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 5q31.1-q32.
 * DOID:0110578
 * autosomal dominant nonsyndromic deafness 71
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * human disease
 * DOID:0080267
 * autosomal dominant nonsyndromic deafness 72
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * human disease
 * DOID:0080268
 * autosomal dominant nonsyndromic deafness 77
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * human disease
 * DOID:0112168
 * autosomal dominant nonsyndromic deafness 79
 * class of disease
 * autosomal dominant nonsyndromic deafness
 * human disease
 * DOID:0112160
 * autosomal dominant optic atrophy and cataract
 * class of disease
 * autosomal dominant optic atrophy optic atrophy autosomal dominant disease
 * gene (19q13.32).
 * DOID:0111433
 * autosomal dominant optic atrophy plus syndrome
 * class of disease
 * autosomal dominant optic atrophy syndrome autosomal dominant disease
 * human disease
 * DOID:0111340
 * autosomal dominant osteopetrosis 1
 * class of disease
 * osteopetrosis autosomal dominant disease
 * human disease
 * DOID:0110937
 * autosomal dominant progressive external ophthalmoplegia 1
 * class of disease
 * autosomal dominant disease chronic progressive external ophthalmoplegia
 * human disease
 * DOID:0111521
 * autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6
 * class of disease
 * autosomal dominant disease chronic progressive external ophthalmoplegia
 * human disease
 * DOID:0111519
 * autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
 * class of disease
 * chronic progressive external ophthalmoplegia autosomal dominant disease
 * human disease
 * DOID:0111517
 * autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
 * class of disease
 * autosomal dominant disease chronic progressive external ophthalmoplegia
 * human disease
 * DOID:0111520
 * autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
 * class of disease
 * chronic progressive external ophthalmoplegia autosomal dominant disease
 * human disease
 * DOID:0111525
 * autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
 * class of disease
 * chronic progressive external ophthalmoplegia autosomal dominant disease
 * human disease
 * DOID:0111518
 * autosomal dominant sensory ataxia 1
 * class of disease
 * hereditary ataxia autosomal dominant disease
 * human disease
 * DOID:0111170
 * autosomal dominant severe congenital neutropenia
 * class of disease
 * severe congenital neutropenia autosomal dominant disease
 * human disease
 * DOID:0112130
 * autosomal dominant spondyloepiphyseal dysplasia tarda
 * class of disease
 * autosomal dominant disease spondyloepiphyseal dysplasia tarda
 * human disease
 * DOID:0112285
 * autosomal dominant thrombophilia due to protein C deficiency
 * class of disease
 * protein C deficiency
 * human disease
 * DOID:0111909
 * autosomal dominant woolly hair
 * class of disease
 * woolly hair autosomal dominant disease
 * human disease
 * DOID:0111573
 * autosomal genetic disease
 * class of disease
 * monogenic disease
 * monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes
 * DOID:0050739
 * Autosomal diseases
 * autosomal hemophilia A
 * class of disease
 * blood coagulation disease autosomal genetic disease hemophilia A
 * human disease
 * DOID:0111823
 * autosomal recessive Alport syndrome
 * class of disease
 * Alport syndrome autosomal recessive disease
 * Alport syndrome that has material -basis in homozygous or compound heterozygous mutation in the COL4A3 or the COL4A4 gene, both of which map to chromosome 2q
 * DOID:0110033
 * autosomal recessive Kenny-Caffey syndrome
 * class of disease
 * Kenny-Caffey syndrome autosomal recessive disease
 * human disease
 * DOID:0080722
 * autosomal recessive Robinow syndrome
 * class of disease
 * Robinow syndrome autosomal recessive disease
 * Human disease
 * DOID:0060764
 * autosomal recessive centronuclear myopathy
 * class of disease
 * centronuclear myopathy autosomal recessive disease
 * inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy
 * DOID:0111216
 * autosomal recessive chronic granulomatous disease cytochrome b-negative
 * class of disease
 * autosomal recessive disease chronic granulomatous disease
 * A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the CYBA gene on chromosome 16q24.2.
 * DOID:0070193
 * autosomal recessive chronic granulomatous disease cytochrome b-positive type I
 * class of disease
 * chronic granulomatous disease autosomal recessive disease
 * A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF1 gene on chromosome 7q11.23.
 * DOID:0070192
 * autosomal recessive chronic granulomatous disease cytochrome b-positive type II
 * class of disease
 * autosomal recessive disease chronic granulomatous disease
 * chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF2 gene on chromosome 1q25
 * DOID:0070191
 * autosomal recessive chronic granulomatous disease cytochrome b-positive type III
 * class of disease
 * autosomal recessive disease chronic granulomatous disease
 * chronic granulomatous disease characterized by that autosomal recessive inheritance has material basis in mutation in the NCF4 gene on chromosome 22q12
 * DOID:0070194
 * autosomal recessive congenital bilateral absence of vas deferens
 * class of disease
 * autosomal recessive disease congenital bilateral aplasia of the vas deferens
 * human disease
 * DOID:0111864
 * autosomal recessive congenital ichthyosis
 * class of disease
 * autosomal recessive disease congenital ichthyosis
 * skin disease that is characterized by autosomal recessive inheritance and abnormal skin scaling over the whole body due to a defect in keratinization
 * DOID:0060655
 * autosomal recessive congenital ichthyosis 1
 * class of disease
 * autosomal recessive congenital ichthyosis
 * An autosomal recessive congenital ichthyosis characterized by lamellar ichthyosis, ectropion, eclabium and hyperkeratosis that has material basis in homozygous or compound heterozygous mutation in the TGM1 gene on chromosome 14q11.2.
 * DOID:0060656
 * autosomal recessive congenital ichthyosis 13
 * class of disease
 * autosomal recessive congenital ichthyosis
 * human disease
 * DOID:0080257
 * autosomal recessive congenital ichthyosis 14
 * class of disease
 * autosomal recessive congenital ichthyosis
 * human disease
 * DOID:0080258
 * autosomal recessive congenital ichthyosis 7
 * class of disease
 * autosomal recessive congenital ichthyosis
 * Human disease
 * DOID:0060716
 * autosomal recessive craniometaphyseal dysplasia
 * class of disease
 * autosomal recessive disease craniometaphyseal dysplasia
 * human disease
 * DOID:0080802
 * autosomal recessive cutis laxa type 2, classic type
 * class of disease
 * cutis laxa autosomal recessive disease autosomal recessive cutis laxa type 2
 * cutis laxa characterized by generalized skin wrinkling, sparse subcutaneous fat, dysmorphic progeroid facial features and severe hypotonia
 * DOID:0070141
 * autosomal recessive cutis laxa type I
 * class of disease
 * cutis laxa autosomal recessive disease
 * cutis laxa characterized by wrinkled, redundant and sagging inelastic skin and severe systemic manifestations particulary in the lungs, vasculature, and gastrointestinal and genitourinary systems
 * DOID:0070144
 * autosomal recessive cutis laxa type IA
 * class of disease
 * autosomal recessive cutis laxa type I
 * autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the FBLN5 gene on chromosome 14q32
 * DOID:0070135
 * autosomal recessive cutis laxa type IB
 * class of disease
 * autosomal recessive cutis laxa type I
 * human disease
 * DOID:0070133
 * autosomal recessive cutis laxa type IC
 * class of disease
 * autosomal recessive cutis laxa type I
 * autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13
 * DOID:0070139
 * autosomal recessive cutis laxa type IIA
 * class of disease
 * autosomal recessive cutis laxa type 2, classic type
 * autosomal recessive cutis laxa type II classic type that has material basis in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24
 * DOID:0070134
 * autosomal recessive cutis laxa type IIB
 * class of disease
 * cutis laxa autosomal recessive disease autosomal recessive cutis laxa type 2
 * A cutis laxa characterized by progeroid features that has material basis in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25.3.
 * DOID:0070137
 * autosomal recessive cutis laxa type IIIA
 * class of disease
 * De Barsy syndrome
 * human disease
 * DOID:0070132
 * autosomal recessive cutis laxa type IIIB
 * class of disease
 * De Barsy syndrome
 * autosomal recessive cutis laxa type III that has material basis in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25
 * DOID:0070138
 * autosomal recessive disease
 * class of disease
 * autosomal genetic disease disease
 * genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop
 * DOID:0050737
 * Autosomal recessive diseases
 * autosomal recessive distal hereditary motor neuronopathy
 * class of disease
 * autosomal recessive disease spinal muscular atrophy
 * spinal muscular atrophy that has material basis in autosomal recessive inheritance
 * DOID:0111197
 * autosomal recessive dyskeratosis congenita 4
 * class of disease
 * dyskeratosis congenita autosomal recessive disease
 * A dyskeratosis congenita that has material basis in an autosomal recessive mutation of TERT on chromosome 5p15.33.
 * DOID:0070021
 * autosomal recessive dyskeratosis congenita 5
 * class of disease
 * dyskeratosis congenita autosomal recessive disease
 * A dyskeratosis congenita that has material basis in an autosomal recessive mutation of RTEL1 on chromosome 20q13.33.
 * DOID:0070022
 * autosomal recessive dyskeratosis congenita 6
 * class of disease
 * dyskeratosis congenita autosomal recessive disease
 * human disease
 * DOID:0070024
 * autosomal recessive early-onset Parkinson disease 23
 * class of disease
 * young-onset Parkinson disease autosomal recessive disease
 * early-onset Parkinson disease that has material basis in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22
 * DOID:0060896
 * autosomal recessive hyaline body myopathy
 * class of disease
 * hyaline body myopathy autosomal recessive disease
 * A hyaline body myopathy that has material basis in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.
 * DOID:0111268
 * autosomal recessive intellectual developmental disorder-72
 * class of disease
 * syndromic intellectual disability
 * human disease
 * DOID:0080765
 * autosomal recessive isolated ectopia lentis 2
 * class of disease
 * isolated ectopia lentis autosomal recessive disease
 * isolated ectopia lentis that has material basis in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21
 * DOID:0111149
 * autosomal recessive limb-girdle muscular dystrophy
 * class of disease
 * limb-girdle muscular dystrophy autosomal recessive disease
 * limb-girdle muscular dystrophy has material basis in autosomal recessive inheritance
 * DOID:0110274
 * autosomal recessive limb-girdle muscular dystrophy type 2B
 * class of disease
 * autosomal recessive limb-girdle muscular dystrophy
 * autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding the skeletal muscle protein dysferlin (DYSF) on chromosome 2p13
 * DOID:0110276
 * autosomal recessive limb-girdle muscular dystrophy type 2C
 * class of disease
 * autosomal recessive limb-girdle muscular dystrophy sarcoglycanopathy qualitative or quantitative defects of gamma-sarcoglycan neuromuscular disease with dilated cardiomyopathy
 * autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12
 * DOID:0110277
 * autosomal recessive limb-girdle muscular dystrophy type 2Z
 * class of disease
 * disorder of O-xylosylglycan synthesis autosomal recessive limb-girdle muscular dystrophy
 * An autosomal recessive condition caused by mutation(s) in the POGLUT1 gene, encoding protein O-glucosyltransferase 1. It is characterized by progressive muscular dystrophy, primarily affecting the proximal muscles, resulting in difficulty walking.
 * DOID:0080762
 * autosomal recessive nonsyndromic deafness 100
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111638
 * autosomal recessive nonsyndromic deafness 106
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0080261
 * autosomal recessive nonsyndromic deafness 107
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0080262
 * autosomal recessive nonsyndromic deafness 108
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0080263
 * autosomal recessive nonsyndromic deafness 109
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111639
 * autosomal recessive nonsyndromic deafness 110
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111644
 * autosomal recessive nonsyndromic deafness 111
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111640
 * autosomal recessive nonsyndromic deafness 112
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111637
 * autosomal recessive nonsyndromic deafness 113
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111636
 * autosomal recessive nonsyndromic deafness 114
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111642
 * autosomal recessive nonsyndromic deafness 115
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111643
 * autosomal recessive nonsyndromic deafness 1A
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has material basis in mutation in the GJB2 gene on chromosome 13q12
 * DOID:0110475
 * autosomal recessive nonsyndromic deafness 27
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 2q23-q31
 * DOID:0110485
 * autosomal recessive nonsyndromic deafness 4
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * autosomal recessive nonsyndromic deafness that has material basis in mutation in the SLC26A4 gene on chromosome 7q22
 * DOID:0110498
 * autosomal recessive nonsyndromic deafness 40
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 22q11.21-q12.1.
 * DOID:0110499
 * autosomal recessive nonsyndromic deafness 5
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12
 * DOID:0110507
 * autosomal recessive nonsyndromic deafness 57
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111635
 * autosomal recessive nonsyndromic deafness 94
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111641
 * autosomal recessive nonsyndromic deafness 99
 * class of disease
 * autosomal recessive nonsyndromic deafness
 * human disease
 * DOID:0111634
 * autosomal recessive osteopetrosis 1
 * class of disease
 * osteopetrosis autosomal recessive disease
 * An osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TCIRG1 gene on chromosome 11q13.2.
 * DOID:0110942
 * autosomal recessive osteopetrosis 3
 * class of disease
 * osteopetrosis autosomal recessive disease renal tubular acidosis
 * osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the CA2 gene on chromosome 8q21
 * DOID:0110941
 * autosomal recessive pericentral pigmentary retinopathy
 * class of disease
 * retinitis pigmentosa autosomal recessive disease
 * retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy
 * DOID:0110422
 * autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2
 * class of disease
 * autosomal recessive disease chronic progressive external ophthalmoplegia
 * human disease
 * DOID:0111515
 * autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
 * class of disease
 * chronic progressive external ophthalmoplegia autosomal recessive disease
 * human disease
 * DOID:0111523
 * autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4
 * class of disease
 * chronic progressive external ophthalmoplegia autosomal recessive disease
 * human disease
 * DOID:0111516
 * autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5
 * class of disease
 * autosomal recessive disease chronic progressive external ophthalmoplegia
 * human disease
 * DOID:0111524
 * autosomal recessive pseudohypoaldosteronism type 1
 * class of disease
 * pseudohypoaldosteronism autosomal recessive disease
 * human disease
 * DOID:0060854
 * autosomal recessive pyridoxine-refractory sideroblastic anemia 3
 * class of disease
 * pyridoxine-refractory autosomal recessive sideroblastic anemia autosomal recessive disease sideroblastic anaemia P
 * sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32
 * DOID:0080343
 * autosomal recessive spinocerebellar ataxia 23
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111613
 * autosomal recessive spinocerebellar ataxia 24
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111615
 * autosomal recessive spinocerebellar ataxia 27
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111616
 * autosomal recessive spinocerebellar ataxia 3
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111612
 * autosomal recessive spinocerebellar ataxia 4
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111611
 * autosomal recessive spinocerebellar ataxia 6
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111617
 * autosomal recessive spinocerebellar ataxia 8
 * class of disease
 * autosomal recessive cerebellar ataxia
 * human disease
 * DOID:0111618
 * autosomal recessive spondyloepiphyseal dysplasia tarda
 * class of disease
 * spondyloepiphyseal dysplasia tarda autosomal recessive disease
 * human disease
 * DOID:0112293
 * autosomal recessive type IV Ehlers-Danlos syndrome
 * class of disease
 * Ehlers-Danlos syndrome autosomal recessive disease
 * Human disease
 * DOID:14759
 * autosomal-mitochondrial sensorineural deafness
 * class of disease
 * digenic disease sensorineural hearing loss
 * human disease
 * DOID:0111752
 * autotopagnosia
 * class of disease
 * agnosia
 * form of agnosia
 * DOID:0060138
 * avoidant personality disorder
 * class of disease
 * personality disorder disease
 * severe form of social anxiety
 * DOID:1509
 * Avoidant personality disorder
 * axial osteomalacia
 * class of disease
 * osteosclerosis osteomalacia genetic disease
 * osteosclerosis that results in coarsening located in trabecular bone
 * DOID:0080039
 * axillary adentis
 * class of disease
 * lymphadenitis
 * Human disease
 * DOID:4640
 * axonal neuropathy
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:7319
 * azoospermia
 * class of disease
 * male infertility oligospermia disease
 * male infertility disease characterized by the absence of any measurable level of sperm in semen
 * DOID:14227
 * C12.200.294.430.380 C12.100.500.430.380 C12.100.750.700.380
 * Azoospermia
 * Semen analysis.JPG
 * aztreonam allergy
 * class of disease
 * beta-lactam allergy
 * beta-lactam allergy that has allergic trigger aztreonam
 * DOID:0040037
 * bacillary angiomatosis
 * class of disease
 * bartonellosis angiomatosis disease
 * human disease
 * DOID:0060345
 * C01.150.252.400.126.100.075 C01.150.252.819.150 C01.800.720.150 C14.907.077.060 C17.800.838.765.150 C17.800.862.060
 * background diabetic retinopathy
 * class of disease
 * diabetic retinopathy
 * Human disease
 * DOID:13208
 * bacterial esophagitis
 * class of disease
 * esophagitis bacterial infectious disease
 * An acute bacterial infection that affects the esophagus. Symptoms include severe pain on swallowing and retrosternal pain. Endoscopic examination reveals esophageal mucosal ulcerations and pseudomembranous formations.
 * DOID:13921
 * bacterial gastritis
 * class of disease
 * gastritis bacterial infectious disease chronic gastritis
 * Gastritis resulting from bacteria
 * DOID:4033
 * bacterial sepsis
 * class of disease
 * bacterial infectious disease sepsis
 * bacterial infectious disease has material basis in Bacteria
 * DOID:0040085
 * bacteriuria
 * class of disease
 * urinary system disease disease
 * medical term denoting the presence of bacteria in urine
 * DOID:1412
 * C01.915.219 C12.200.777.892.219 C12.050.351.968.892.219 C12.950.892.219
 * Bacteriuria pyuria 4.jpg
 * bagassosis
 * class of disease
 * extrinsic allergic alveolitis
 * silicosis
 * DOID:12522
 * balanitis
 * class of disease symptom or sign
 * penile disease inflammatory disease disease
 * infectious or non-infectious inflammation of the glans penis
 * DOID:13033
 * C12.294.494.136
 * Balanitis
 * Inflammation of the glans penis and the preputial mucosa.jpg
 * balanitis xerotica obliterans
 * class of disease
 * balanitis
 * Human disease
 * DOID:13477
 * C12.294.494.136.500
 * Balanitis xerotica obliterans
 * Balanitis xerotica obliterans.jpg
 * balanoposthitis
 * class of disease
 * penile disease balanitis posthitis
 * human disease
 * DOID:13031
 * Balanoposthitis
 * baldness
 * class of disease
 * hair diseases hairstyle hair anomaly absence disease
 * state where most or all of hair from the head has been lost or intentionally removed
 * DOID:987
 * Baldness
 * PatrickStewart2004-08-03.jpg
 * balloon cell malignant melanoma
 * class of disease
 * skin melanoma
 * Human disease
 * DOID:10044
 * band keratopathy
 * class of disease
 * corneal degeneration
 * Human disease
 * DOID:11164
 * Band keratopathy
 * barbiturate abuse
 * class of disease
 * substance abuse
 * substance abuse that involves the recurring use of barbiturate drugs despite negative consequences
 * DOID:8519
 * barbiturate dependence
 * class of disease
 * barbiturate abuse substance dependence
 * drug dependence that involves the continued use of barbiturates despite problems related to use of the substance
 * DOID:2575
 * basal ganglia cerebrovascular disease
 * class of disease
 * basal ganglia disease cerebrovascular disease
 * Human disease
 * DOID:10991
 * C10.228.140.079.127 C10.228.140.300.100 C14.907.253.061
 * basal ganglia disease
 * class of disease
 * encephalopathy
 * brain disease that is characterized by dysfunction of the basal ganglia which help start and control movement
 * DOID:679
 * C10.228.140.079
 * basal-cell carcinoma
 * class of disease
 * skin cancer skin carcinoma basal-cell neoplasm disease
 * subtype of basal-cell carcinoma most commonly occurring on the sun-exposed areas of the head and neck
 * DOID:2513
 * C04.557.470.200.165 C04.557.470.565.165
 * Basal-cell carcinoma
 * Basaliom1.jpg
 * basaloid large cell carcinoma of the lung
 * class of disease
 * large-cell lung carcinoma squamous cell carcinoma of the lung basaloid carcinoma
 * human disease
 * DOID:7045
 * basaloid squamous cell carcinoma
 * class of disease
 * squamous cell carcinoma basaloid carcinoma basal-cell carcinoma
 * Human disease
 * DOID:5522
 * basaloid squamous cell skin carcinoma
 * class of disease
 * basaloid squamous cell carcinoma keratinizing squamous cell carcinoma skin cancer squamous cell carcinoma
 * Human disease
 * DOID:7049
 * basidiobolomycosis
 * class of disease
 * subcutaneous mycosis zygomycosis
 * Human disease
 * DOID:0050278
 * basilar artery insufficiency
 * class of disease
 * transient cerebral isolation vertebrobasilar insufficiency syndrome artery disease
 * human disease
 * DOID:223
 * basilar artery occlusion
 * class of disease
 * occlusion precerebral artery artery disease
 * Human disease
 * DOID:13446
 * basosquamous carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:5063
 * C04.557.470.200.170 C04.557.470.565.170
 * baylisascariasis
 * class of disease
 * parasitic helminthiasis infectious disease spinal cord disease eye disease intestinal disease encephalopathy
 * Human disease
 * DOID:0050259
 * benign adult familial myoclonic epilepsy
 * class of disease
 * myoclonic epilepsy adolescence-adult electroclinical syndrome
 * human disease
 * DOID:0111689
 * benign blood vessel neoplasm
 * class of disease
 * vascular neoplasm cardiovascular organ benign neoplasm
 * benign neoplasm arising from arteries or veins
 * DOID:60006
 * Benign vascular neoplasms
 * benign breast adenomyoepithelioma
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:1641
 * benign breast phyllodes tumor
 * class of disease
 * breast benign neoplasm phyllodes tumor
 * Human disease
 * DOID:1631
 * benign deep fibrous histiocytoma
 * class of disease
 * immune system organ benign neoplasm sclerosing hemangioma
 * Human disease
 * DOID:4419
 * benign dermal neurilemmoma
 * class of disease
 * skin benign neoplasm
 * Human disease
 * DOID:7181
 * benign eccrine breast spiradenoma
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:1616
 * benign ependymoma
 * class of disease
 * benign glioma ependymoma
 * human disease
 * DOID:4844
 * benign epilepsy with centrotemporal spikes
 * class of disease
 * childhood electroclinical syndrome epilepsy syndrome
 * the most common epilepsy syndrome in childhood which usually subsides with age
 * DOID:3329
 * C10.228.140.490.360.280 C10.228.140.490.493.250
 * benign essential hypertension
 * class of disease
 * essential hypertension
 * Human disease
 * DOID:10913
 * benign fibrous mesothelioma
 * class of disease
 * benign mesothelioma solitary fibrous tumor of the pleura
 * human disease
 * DOID:2653
 * C04.557.450.565.590.797.750 C04.588.894.797.640.800
 * benign hypertensive renal disease
 * class of disease
 * renal hypertension
 * Human disease
 * DOID:11520
 * benign intermediate mesothelioma
 * class of disease
 * benign mesothelioma
 * human disease
 * DOID:5884
 * benign lymphoepithelial lesion of salivary gland
 * class of disease
 * salivary gland disease disease
 * Human disease
 * DOID:12899
 * benign mammary dysplasia
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:9504
 * Benign mammary dysplasias
 * benign mastocytoma
 * class of disease
 * benign neoplasms by histologic type
 * human disease
 * DOID:4658
 * benign mediastinal neurilemmoma
 * class of disease
 * benign neurilemmoma mediastinal neurilemmoma benign neoplasm of mediastinum
 * Human disease
 * DOID:7922
 * benign mediastinal psammomatous neurilemmoma
 * class of disease
 * benign mediastinal neurilemmoma
 * Human disease
 * DOID:7921
 * benign meningioma
 * class of disease
 * meningioma benign neoplasm of meninges central nervous system organ benign neoplasm
 * Human disease
 * DOID:4587
 * benign mesothelioma
 * class of disease
 * angiomyolipoma
 * cell type benign neoplasm that has material basis in mesothelium
 * DOID:2645
 * benign neonatal seizures
 * class of disease
 * neonatal period electroclinical syndrome
 * Human disease
 * DOID:14264
 * C10.228.140.490.370 C16.614.258
 * benign neoplasm
 * class of disease
 * disease of cellular proliferation neoplasm disease
 * disease of cellular proliferation that results in abnormal growths in the body which lack the ability to metastasize
 * DOID:0060072
 * Benign neoplasms
 * benign neoplasm of exocrine pancreas
 * class of disease
 * pancreatic exocrine neoplasm benign neoplasm of pancreas endocrine organ benign neoplasm
 * benign neoplasm that involves the exocrine pancreas
 * DOID:0080781
 * benign neoplasm of lymph node
 * class of disease
 * lymph node neoplasm immune system organ benign neoplasm
 * benign neoplasm that involves the lymph node
 * DOID:0080617
 * Benign neoplasms of lymph nodes
 * benign neoplasms by histologic type
 * class of disease
 * benign neoplasm neoplasms by histologic type
 * benign neoplasm that is classified by the type of cell or tissue from which it is derived
 * DOID:0060084
 * benign neurilemmoma
 * class of disease
 * neurilemmoma
 * Human disease
 * DOID:955
 * benign ovarian sex cord-stromal tumor
 * class of disease
 * ovarian sex cord-stromal tumor sex cord-stromal benign neoplasm
 * sex cord-stromal tumor arising from the ovary, without metastatic potential
 * DOID:0080370
 * benign parathyroid gland neoplasm
 * class of disease
 * parathyroid neoplasm endocrine organ benign neoplasm parathyroid gland disease
 * benign neoplasm that involves the parathyroid gland
 * DOID:60008
 * Benign neoplasms of parathyroid gland
 * benign paroxysmal positional nystagmus
 * class of disease
 * peripheral vertigo disease
 * human disease
 * DOID:13941
 * C09.218.568.900.883.500 C10.597.951.500 C23.888.592.958.500
 * Balance Disorder Illustration A.png
 * benign pericardial teratoma
 * class of disease
 * mature teratoma benign neoplasm of pericardium rare circulatory system disease cardiovascular organ benign neoplasm pericardium disease
 * Human disease
 * DOID:8012
 * benign peritoneal mesothelioma
 * class of disease
 * peritoneal benign neoplasm
 * human disease
 * DOID:1789
 * benign perivascular tumor
 * class of disease
 * cardiovascular organ benign neoplasm perivascular tumor
 * Human disease
 * DOID:5238
 * benign pleural mesothelioma
 * class of disease
 * pleural cancer respiratory system benign neoplasm pleural disease benign neoplasms by histologic type
 * human disease
 * DOID:5157
 * benign prostate phyllodes tumor
 * class of disease
 * male reproductive organ benign neoplasm prostate phyllodes tumor
 * Human disease
 * DOID:2885
 * benign recurrent intrahepatic cholestasis 1
 * class of disease
 * benign recurrent intrahepatic cholestasis autosomal recessive disease
 * benign recurrent intrahepatic cholestasis characterized by typically autosomal recessive inheritance that has material basis in mutation in the ATP8B1 gene on chromosome 18q
 * DOID:0070231
 * benign recurrent intrahepatic cholestasis 2
 * class of disease
 * benign recurrent intrahepatic cholestasis autosomal recessive disease
 * benign recurrent intrahepatic cholestasis characterized by autosomal recessive inheritance that has material basis in mutation in the ABCB11 gene on chromosome 2q31
 * DOID:0070232
 * benign renovascular hypertension
 * class of disease
 * benign secondary hypertension renal hypertension renovascular hypertension
 * Human disease
 * DOID:13145
 * benign secondary hypertension
 * class of disease
 * secondary hypertension
 * Human disease
 * DOID:13143
 * benign shuddering attacks
 * class of disease
 * movement disorders myoclonus
 * Human disease
 * DOID:1713
 * benign struma ovarii
 * class of disease
 * struma ovarii ovarian benign neoplasm
 * Human disease
 * DOID:5209
 * benign teratoma
 * class of disease
 * germ cell benign neoplasm
 * human disease
 * DOID:0080602
 * benign vaginal carcinosarcoma
 * class of disease
 * vaginal benign neoplasm
 * Human disease
 * DOID:135
 * benzo[d]isothiazol-3-one allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger benzo[d]isothiazol-3-one
 * DOID:0040075
 * benzoic acid allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger benzoic acid
 * DOID:0040057
 * benzylpenicillin allergy
 * class of disease
 * beta-lactam allergy
 * beta-lactam allergy that has allergic trigger benzylpenicillin
 * DOID:0040003
 * beriberi
 * class of disease
 * nutritional deficiency disease thiamine deficiency disease
 * nutritional thiamine deficiency disease in humans
 * DOID:13725
 * C18.654.521.500.133.699.827.223
 * Beriberi
 * Late stage of paralysis with atrophy in dry beriberi.jpg
 * berylliosis
 * class of disease
 * pneumoconiosis occupational lung disease Beryllium poisoning respiratory allergy disease
 * pneumoconiosis that involves allergic response located in lungs caused by inhalation of beryllium compounds
 * DOID:10322
 * C08.381.483.581.225 C08.381.520.702.225 C24.800.225
 * Berylliosis
 * Chronic beryllioisis - Case 293 (15342093149).jpg
 * beta-lactam allergy
 * class of disease
 * drug allergy
 * drug allergy triggered by a beta-lactam
 * DOID:0060519
 * beta-thalassemia intermedia
 * class of disease
 * beta thalassemia
 * Beta-thalassemia (BT) intermedia is a form of BT (see this term) characterized by mild to moderate anemia which does not or only occasionally requires transfusion
 * DOID:0080772
 * beta-thalassemia major
 * class of disease
 * beta thalassemia
 * Beta-thalassemia (BT) major is a severe early-onset form of BT (see this term) characterized by severe anemia requiring regular red blood cell transfusions
 * DOID:0080771
 * bicipital tenosynovitis
 * class of disease
 * tenosynovitis
 * Human disease
 * DOID:14192
 * bilateral breast cancer
 * class of disease
 * breast carcinoma
 * breast carcinoma that is characterized by an individual having breast cancer in both breasts, either simultaneously or at different times
 * DOID:6741
 * bilateral frontoparietal polymicrogyria
 * class of disease
 * autosomal recessive disease
 * human disease
 * DOID:0080922
 * bilateral hyperactive labyrinth
 * class of disease
 * labyrinthine dysfunction
 * Human disease
 * DOID:14165
 * bilateral optic nerve hypoplasia
 * class of disease
 * autosomal dominant disease optic nerve disease optic nerve hypoplasia
 * human disease
 * DOID:0111531
 * bilateral renal aplasia
 * class of disease
 * renal agenesis
 * renal agenesis that is characterized by the absence of both kidneys at birth
 * DOID:0080200
 * bile duct adenocarcinoma
 * class of disease
 * bile duct carcinoma adenocarcinoma of liver and intrahepatic biliary tract adenocarcinoma
 * bile duct carcinoma that derives from epithelial cells of glandular origin
 * DOID:4896
 * bile duct adenoma
 * class of disease
 * liver neoplasm biliary tract neoplasm bile duct disease gastrointestinal adenoma benign neoplasms by histologic type adenoma
 * adenoma and biliary tract cancer that results in a small firm white nodule with multiple bile ducts that are located in a fibrous stroma
 * DOID:5381
 * C04.557.470.035.085
 * bile duct cancer
 * class of disease
 * biliary tract cancer bile duct neoplasm bile duct disease
 * biliary tract cancer that is located in the bile duct
 * DOID:4606
 * bile duct carcinoma
 * class of disease
 * bile duct cancer carcinoma
 * bile duct cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:4897
 * bile duct carcinoma in situ
 * class of disease
 * in situ carcinoma biliary tract neoplasm bile duct disease
 * Human disease
 * DOID:0050613
 * bile duct clear cell adenocarcinoma
 * class of disease
 * bile duct adenocarcinoma clear cell adenocarcinoma extrahepatic bile duct adenocarcinoma
 * Human disease
 * DOID:7032
 * bile duct cystadenocarcinoma
 * class of disease
 * bile duct adenocarcinoma bile duct cystadenoma
 * Human disease
 * DOID:4075
 * bile duct cystadenoma
 * class of disease
 * bile duct adenoma bile duct disease biliary tract neoplasm benign neoplasms by histologic type
 * Human disease
 * DOID:5384
 * bile duct disease
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:4138
 * C06.130.120
 * bile duct mucinous adenocarcinoma
 * class of disease
 * bile duct adenocarcinoma extrahepatic bile duct adenocarcinoma mucinous adenocarcinoma
 * Human disease
 * DOID:3698
 * bile duct mucoepidermoid carcinoma
 * class of disease
 * mucoepidermoid carcinoma bile duct mucinous adenocarcinoma bile duct cancer
 * Human disease
 * DOID:4681
 * bile duct rhabdomyosarcoma
 * class of disease
 * bile duct sarcoma rhabdomyosarcoma bile duct cancer
 * rhabdomyosarcoma and sarcoma of bile duct that is located in the bile duct
 * DOID:3254
 * bile duct sarcoma
 * class of disease
 * bile duct cancer sarcoma
 * sarcoma and malignant tumor of extrahepatic bile duct that is located in the bile duct
 * DOID:4064
 * bile duct signet ring cell carcinoma
 * class of disease
 * signet ring cell adenocarcinoma bile duct carcinoma extrahepatic bile duct adenocarcinoma
 * Human disease
 * DOID:3494
 * bile reflux
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:12237
 * C06.130.140 C06.405.748.240.140
 * biliary dyskinesia
 * class of disease
 * gallbladder disease common bile duct disease
 * gallbladder disease characterized by altered tonus of the sphincter of Oddi, disturbance in the coordination of contraction of the biliary ducts, and/or reduction in the speed of emptying of the biliary tree
 * DOID:4140
 * C06.130.120.250.098
 * biliary papillomatosis
 * class of disease
 * biliary tract neoplasm papilloma
 * biliary tract neoplasm characterized by multiple papillary tumors in the intrahepatic and/or extrahepatic biliary tree
 * DOID:5468
 * Intraductal papillary neoplasm of the bile duct
 * BileDuct IntraductalPapillaryNeoplasm MP CTR.jpg
 * biliary reflux
 * class of disease
 * duodenal disease stomach disease gastroesophageal reflux disease
 * human disease
 * DOID:4071
 * C06.405.469.275.700 C06.405.748.240
 * Biliary reflux
 * biliary tract cancer
 * class of disease
 * hepatobiliary system cancer biliary tract neoplasm
 * gastrointestinal system cancer that results in malignant growth located in the gallbladder or located in the bile duct
 * DOID:4607
 * Biliary tract cancers
 * biliary tract disease
 * class of disease
 * biliary disease hepatobiliary disease
 * disease involving the biliary tree
 * DOID:9741
 * C06.130
 * biliary tract intraductal papillary mucinous neoplasm
 * class of disease
 * biliary tract neoplasm
 * human disease
 * DOID:5469
 * biliary tract neoplasm
 * class of disease
 * hepatobiliary neoplasm biliary tract disease
 * hepatobiliary neoplasm located in the biliary tract
 * DOID:0050625
 * C04.588.274.120 C06.130.320 C06.301.120
 * Biliary tract neoplasms
 * bilirubin metabolic disorder
 * class of disease
 * inherited metabolic disorder hyperbilirubinemia
 * inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism
 * DOID:2741
 * C16.320.565.300 C18.452.648.300
 * binocular vision disease
 * class of disease
 * strabismus vision disorder
 * human disease
 * DOID:12667
 * biotin deficiency
 * class of disease
 * nutritional deficiency disease vitamin deficiency disease
 * nutritional deficiency disease that is characterized by thinning of the hair (often with loss of hair color), and red scaly rash around the eyes, nose, and mouth
 * DOID:0050810
 * biotinidase deficiency
 * class of disease
 * multiple carboxylase deficiency disorder of other vitamins and cofactors metabolism and transport rare genetic epilepsy rare hereditary metabolic disease with peripheral neuropathy
 * multiple carboxylase deficiency that involves a deficiency in biotinidase
 * DOID:856
 * C16.320.565.100.620.100 C16.320.565.202.720.100 C18.452.648.100.620.100 C18.452.648.202.720.100
 * Biotin structure.svg
 * biphasic synovial sarcoma
 * class of disease
 * synovial sarcoma
 * Human disease
 * DOID:5492
 * bipolar I disorder
 * class of disease
 * bipolar disorder disease
 * bipolar disorder that is characterized by at least one manic or mixed episode
 * DOID:14042
 * bipolar II disorder
 * class of disease
 * bipolar disorder disease
 * bipolar disorder that is characterized by at least one hypomanic episode and at least one major depressive episode; with this disorder, depressive episodes are more frequent and more intense than manic episodes
 * DOID:0060166
 * bipolar disorder
 * class of disease
 * mood disorder
 * human mental illness characterized by mood changes
 * DOID:3312
 * F03.084.500
 * Bipolar disorder
 * Comedy and tragedy masks without background.svg
 * bird fancier's lung
 * class of disease
 * extrinsic allergic alveolitis rare allergic respiratory disease
 * extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta, symptoms are abrupt onset of dyspnea, cough, malaise, and fever after exposure to antigen
 * DOID:13891
 * C08.381.483.125.125 C08.674.055.125 C20.543.480.680.075.125 C24.125
 * birdshot chorioretinopathy
 * class of disease
 * uveitis white dot syndrome posterior uveitis non-infectious posterior uveitis
 * human disease
 * DOID:0111079
 * C11.768.773.348.500 C11.941.160.478.400.500 C11.941.879.780.900.300.318.500 C11.941.879.780.900.650.250 C20.111.303
 * Birdshot chorioretinopathy
 * bizarre leiomyoma
 * class of disease
 * leiomyoma
 * Human disease
 * DOID:5127
 * black piedra
 * class of disease
 * superficial mycosis disease
 * superficial mycosis that is a superficial fungal infection of the hair shaft caused by Piedraia hortae
 * DOID:12711
 * Black piedra
 * bladder adenocarcinoma
 * class of disease
 * bladder carcinoma adenocarcinoma
 * bladder carcinoma that derives from epithelial cells of glandular origin
 * DOID:3711
 * Adenocarcinomas of the urinary bladder
 * bladder benign neoplasm
 * class of disease
 * urinary system benign neoplasm bladder disease
 * human disease
 * DOID:0050623
 * bladder calculus
 * class of disease
 * urolithiasis bladder disease
 * stone found in the urinary bladder
 * DOID:11355
 * C12.777.829.720 C12.777.967.500.925 C13.351.968.829.521 C13.351.968.967.500.925 C23.300.175.850.875
 * Urinary bladder stones
 * Bladder Stone 08783.jpg
 * bladder cancer
 * class of disease
 * urinary system cancer bladder disease bladder neoplasm disease
 * urinary system cancer that results in malignant growth located in the urinary bladder
 * DOID:11054
 * Urinary bladder cancer
 * Bladder urothelial carcinoma histopathology (2) at trigone.jpg
 * bladder carcinoma
 * class of disease
 * bladder cancer carcinoma
 * urinary bladder cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:4007
 * bladder carcinoma in situ
 * class of disease
 * non-invasive bladder urothelial carcinoma bladder flat intraepithelial lesion carcinoma in situ of breast and genitourinary system bladder disease in situ carcinoma
 * Human disease
 * DOID:9053
 * bladder clear cell adenocarcinoma
 * class of disease
 * bladder adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5306
 * bladder colloid adenocarcinoma
 * class of disease
 * bladder adenocarcinoma
 * Human disease
 * DOID:3710
 * bladder colonic type adenocarcinoma
 * class of disease
 * bladder adenocarcinoma
 * Human disease
 * DOID:6594
 * bladder diffuse clear cell adenocarcinoma
 * class of disease
 * bladder clear cell adenocarcinoma
 * Human disease
 * DOID:6210
 * bladder disease
 * class of disease
 * urinary system disease
 * urinary system disease that is located in the bladder
 * DOID:365
 * C12.777.829 C13.351.968.829
 * Diseases and disorders of the urinary bladder
 * bladder diverticulum
 * class of disease
 * bladder disease diverticulum genetic disease
 * Human disease
 * DOID:11353
 * Bladder diverticulum
 * bladder dome cancer
 * class of disease
 * bladder cancer
 * human disease
 * DOID:11820
 * bladder exstrophy
 * class of disease
 * bladder disease bladder exstrophy-epispadias-cloacal exstrophy complex disease
 * congenital disorder of urinary system
 * DOID:0080174
 * C12.706.132 C12.777.829.132 C13.351.875.132 C13.351.968.829.132 C16.131.939.132
 * Bladder exstrophy
 * Classical bladder exstrophy.jpg
 * bladder exstrophy-epispadias-cloacal exstrophy complex
 * class of disease
 * congenital disorder urinary system disease
 * physical disorder that is characterized as a spectrum of anomalies involving the urinary tract, genital tract, musculoskeletal system and sometimes the intestinal tract
 * DOID:0080173
 * bladder flat intraepithelial lesion
 * class of disease
 * bladder benign neoplasm bladder cancer
 * Human disease
 * DOID:5429
 * bladder hepatoid adenocarcinoma
 * class of disease
 * bladder adenocarcinoma hepatoid adenocarcinoma
 * Human disease
 * DOID:8097
 * bladder lateral wall cancer
 * class of disease
 * bladder cancer
 * Human disease
 * DOID:11593
 * bladder leiomyoma
 * class of disease
 * bladder benign neoplasm leiomyoma
 * Human disease
 * DOID:13109
 * bladder lymphoma
 * class of disease
 * bladder cancer primary organ-specific lymphoma lymphoma
 * human disease
 * DOID:11821
 * bladder mixed adenocarcinoma
 * class of disease
 * bladder adenocarcinoma
 * Human disease
 * DOID:8096
 * bladder neck cancer
 * class of disease
 * bladder cancer
 * human disease
 * DOID:11809
 * bladder neck obstruction
 * class of disease
 * urinary tract obstruction bladder disease bladder outlet obstruction
 * Human disease
 * DOID:13948
 * C12.777.767.700.962 C12.777.829.760 C13.351.968.767.700.850 C13.351.968.829.601
 * bladder papillary clear cell adenocarcinoma
 * class of disease
 * bladder clear cell adenocarcinoma
 * Human disease
 * DOID:8051
 * bladder papillary transitional cell neoplasm
 * class of disease
 * urinary tract papillary transitional cell benign neoplasm bladder cancer
 * Human disease
 * DOID:5432
 * bladder sarcoma
 * class of disease
 * bladder cancer sarcoma
 * sarcoma and malignant neoplasm of urinary bladder that is located in the bladder
 * DOID:11812
 * bladder signet ring cell adenocarcinoma
 * class of disease
 * bladder adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:6481
 * bladder squamous cell carcinoma
 * class of disease
 * bladder carcinoma squamous cell carcinoma
 * carcinoma of bladder that is manifested in squamous cells of the bladder
 * DOID:3742
 * bladder squamous papilloma
 * class of disease
 * bladder benign neoplasm
 * Human disease
 * DOID:13110
 * bladder transitional cell papilloma
 * class of disease
 * bladder papillary transitional cell neoplasm transitional papilloma urinary tract non-invasive transitional cell neoplasm urinary system benign neoplasm
 * Human disease
 * DOID:6933
 * bladder trigone cancer
 * class of disease
 * bladder cancer bladder dome cancer
 * Human disease
 * DOID:11813
 * bladder tubulo-cystic clear cell adenocarcinoma
 * class of disease
 * bladder clear cell adenocarcinoma
 * Human disease
 * DOID:8050
 * bladder urachal adenocarcinoma
 * class of disease
 * bladder urachal carcinoma bladder adenocarcinoma urachal cancer
 * Human disease
 * DOID:7694
 * bladder urachal carcinoma
 * class of disease
 * bladder carcinoma urachal cancer
 * Human disease
 * DOID:5958
 * bladder urachal squamous cell carcinoma
 * class of disease
 * bladder urachal carcinoma bladder squamous cell carcinoma squamous cell carcinoma
 * Human disease
 * DOID:5957
 * bladder urachal urothelial carcinoma
 * class of disease
 * bladder urachal carcinoma bladder urothelial carcinoma
 * Human disease
 * DOID:7244
 * bladder urothelial carcinoma
 * class of disease
 * bladder carcinoma transitional cell carcinoma
 * bladder carcinoma that has material basis in transitional cells located in the lining of the bladder
 * DOID:4006
 * bladder urothelial papillary carcinoma
 * class of disease
 * bladder urothelial carcinoma bladder papillary transitional cell neoplasm papillary transitional carcinoma
 * Human disease
 * DOID:6975
 * bladder verrucous squamous cell carcinoma
 * class of disease
 * bladder squamous cell carcinoma verrucous carcinoma
 * Human disease
 * DOID:3741
 * blastema predominant kidney Wilms' tumor
 * class of disease
 * nephroblastoma
 * Human disease
 * DOID:5182
 * blastoma
 * class of disease
 * cell type cancer disease
 * A cell type cancer that has material basis in abnormally proliferating cells derived from precursor cells called blast cells.
 * DOID:0070003
 * Blastomas
 * blepharitis
 * class of disease symptom or sign
 * eyelid disease eye inflammation inflammatory disease disease
 * eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow
 * DOID:9423
 * C11.338.133
 * Blepharitis
 * Infant with blepharitis on the right side.jpg
 * blepharochalasis
 * class of disease
 * eyelid disease
 * eyelid disease that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over the lid margins
 * DOID:348
 * blepharocheilodontic syndrome 1
 * class of disease
 * Blepharo-cheilo-odontic syndrome
 * blepharocheilodontic syndrome that has material basis in heterozygous mutation in the CDH1 gene on chromosome 16q22
 * DOID:0080345
 * blepharocheilodontic syndrome 2
 * class of disease
 * Blepharo-cheilo-odontic syndrome
 * blepharocheilodontic syndrome that has material basis in heterozygous mutation in the CTNND1 gene on chromosome 11q12
 * DOID:0080346
 * blepharoconjunctivitis
 * class of disease
 * blepharitis conjunctivitis
 * blepharitis that is characterized by the dual combination of conjunctivitis with blepharitis
 * DOID:2456
 * blepharophimosis
 * class of disease
 * eyelid disease congenital physical abnormality disease
 * Human disease
 * DOID:10348
 * C11.250.090 C11.338.190 C16.131.384.190
 * Blepharophimosis
 * Blepharophimosis.png
 * blepharospasm
 * class of disease
 * focal dystonia cranio-facial dystonia disease
 * focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks
 * DOID:529
 * C11.338.250
 * Gray379.png
 * blind hypertensive eye
 * class of disease
 * eye degenerative disease glaucoma
 * human disease
 * DOID:11776
 * blind loop syndrome
 * class of disease
 * intestinal disease small intestinal bacterial overgrowth
 * intestinal disease characterized by a dysbalance of the bacterial flora of the small intestine, causing derangement to the normal physiological processes of digestion and absorption
 * DOID:10606
 * C06.405.469.637.145 C18.452.603.145
 * blindness
 * class of disease symptom or sign
 * visual impairment eye disease vision symptom sensory disability
 * complete or nearly complete lack of vision; visual acuity worse than 3/60
 * DOID:1432
 * C10.597.751.941.162 C11.966.075 C23.888.592.763.941.162
 * Visual impairment
 * Watch for the blind.jpg
 * blood coagulation disease
 * class of disease symptom or sign
 * hematopoietic system disease hemic system symptom disease
 * condition in which the blood’s ability to coagulate (form clots) is impaired
 * DOID:1247
 * C15.378.100
 * blood group incompatibility
 * class of disease
 * hematopoietic system disease transfusion incident
 * Human disease
 * DOID:4176
 * G09.188.114 G12.186
 * blood platelet disease
 * class of disease
 * hematopoietic system disease blood coagulation disease
 * disorder of platelet function
 * DOID:2218
 * C15.378.140
 * blood protein disease
 * class of disease
 * hematopoietic system disease
 * human disease
 * DOID:620
 * C15.378.147
 * blue toe syndrome
 * class of disease
 * foot diseases cyanosis cholesterol embolism
 * Human disease
 * DOID:14121
 * C14.907.355.350.454.500.200 C14.907.617.249
 * blunt duct adenosis of breast
 * class of disease
 * microglandular adenosis non-proliferative fibrocystic change of the breast
 * Human disease
 * DOID:5996
 * body dysmorphic disorder
 * class of disease
 * somatoform disorder hypochondriasis disease
 * mental disorder
 * DOID:0060163
 * F03.875.149
 * Body dysmorphic disorder
 * bone Ewing's sarcoma
 * class of disease
 * Ewing sarcoma
 * peripheral primitive neuroectodermal tumor that is located in bone
 * DOID:3368
 * bone ameloblastoma
 * class of disease
 * bone benign neoplasm ameloblastoma
 * bone benign neoplasm that has material basis in odontogenic epithelium and is located in bone
 * DOID:0050895
 * bone angioendothelial sarcoma
 * class of disease
 * osteosarcoma vascular bone neoplasm bone sarcoma
 * Human disease
 * DOID:3351
 * bone benign neoplasm
 * class of disease
 * connective tissue benign neoplasm bone disease bone neoplasm musculoskeletal system benign neoplasm
 * connective tissue benign neoplasm that is located in bone
 * DOID:0060094 DOID:0060120
 * bone cancer
 * class of disease
 * connective tissue neoplasm bone disease rare tumor rare bone disease musculoskeletal system cancer bone neoplasm
 * connective tissue cancer that is located in bone and is characterized by uncontrolled cellular proliferation that destroys normal bone tissue
 * DOID:184
 * Cancers of bone and articular cartilage
 * bone carcinoma
 * class of disease
 * bone cancer carcinoma
 * bone cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:2762
 * bone chondrosarcoma
 * class of disease
 * chondrosarcoma
 * chondrosarcoma that is located in bone
 * DOID:0050897
 * bone deterioration disease
 * class of disease
 * bone structure disease
 * bone structure disease that results in change or damage of structure located in bone
 * DOID:0080007
 * bone development disease
 * class of disease
 * bone disease
 * bone disease that results in abnormal growth and development located in bone or located in cartilage
 * DOID:0080006
 * C05.116.099
 * bone disease
 * class of disease
 * connective tissue disease
 * medical condition which affects the bone
 * DOID:0080001
 * C05.116
 * Osteopathies
 * bone epithelioid hemangioma
 * class of disease
 * bone benign neoplasm histiocytoid hemangioma
 * Human disease
 * DOID:6610
 * bone giant cell sarcoma
 * class of disease
 * malignant giant cell tumor bone sarcoma
 * malignant giant cell tumor that is composed of multinucleated giant cells
 * DOID:4719
 * bone inflammation disease
 * class of disease
 * bone disease inflammation disease
 * inflammation of bone
 * DOID:3342
 * C05.116.680
 * bone leiomyosarcoma
 * class of disease
 * osteosarcoma leiomyosarcoma
 * Human disease
 * DOID:3367
 * bone lymphoma
 * class of disease
 * bone cancer primary organ-specific lymphoma lymphoma
 * bone cancer and lymphoma by site that results in lymphoma starting in the bone
 * DOID:6759
 * bone marrow disease
 * class of disease
 * hematopoietic system disease bone disease
 * human disease
 * DOID:4961
 * C15.378.190
 * bone osteosarcoma
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3376
 * bone peripheral neuroepithelioma
 * class of disease
 * bone Ewing's sarcoma
 * Human disease
 * DOID:4388
 * bone remodeling disease
 * class of disease
 * bone disease
 * bone disease that results in formation or resorption abnormalities located in bone
 * DOID:0080005
 * bone resorption disease
 * class of disease
 * bone remodeling disease
 * human disease
 * DOID:0080011
 * bone sarcoma
 * class of disease
 * sarcoma bone cancer bone neoplasm
 * a sarcoma that arises from the bone, for example osteosarcoma and chondrosarcoma
 * DOID:0080639
 * bone squamous cell carcinoma
 * class of disease
 * bone carcinoma squamous cell carcinoma
 * bone carcinoma that derives from squamous epithelial cells
 * DOID:0050896
 * bone structure disease
 * class of disease
 * bone disease spinal disease
 * bone disease that has material basis in an abnormality in the location or function of the skeletal structure
 * DOID:0080010
 * borderline glaucoma
 * class of disease
 * glaucoma
 * Human disease
 * DOID:9283
 * borderline personality disorder
 * class of disease
 * personality disorder disease
 * personality disorder characterized by variability of moods and unstable relationships
 * DOID:10930
 * F03.675.100
 * Borderline personality disorder
 * BPD 1.png
 * botryoid embryo rhabdomyosarcoma
 * class of disease
 * embryonal rhabdomyosarcoma
 * Human disease
 * DOID:3255
 * bowel dysfunction
 * class of disease
 * intestinal disease
 * Human disease
 * DOID:9779
 * bowel obstruction
 * class of disease
 * intestinal disease disease
 * Human disease
 * DOID:8437
 * C06.405.469.531
 * Intestinal obstruction
 * Upright abdominal X-ray demonstrating a bowel obstruction.jpg
 * brachial plexus lesion
 * class of disease
 * brachial plexus neuropathy nerve injury neck injury disease
 * brachial plexus neuropathy characterized by an abnormality, usually caused by disease or trauma, located in the brachial plexus
 * DOID:8443
 * Brachial plexus injury
 * brachial plexus neoplasm
 * class of disease
 * nerve plexus neoplasm brachial plexus neuropathy central nervous system cancer
 * neoplasm (disease) that involves the brachial nerve plexus
 * DOID:5913
 * brachial plexus neuritis
 * class of disease
 * neuritis brachial plexus neuropathy
 * An inflammatory process affecting the brachial plexus. It results in severe pain in the upper extremity and shoulder, upper arm weakness and loss of sensation in the upper arm.
 * DOID:3689
 * C10.668.829.100.500 C10.668.829.650.250
 * brachial plexus neuropathy
 * class of disease
 * plexopathy peripheral neuropathy
 * brachial plexus disorder characterized by regional paresthesia, pain and muscle weakness, and limited movement in the arm or hand
 * DOID:3690
 * C10.668.829.100
 * Brachial plexus neuropathies
 * brachydactyly
 * class of disease
 * dysostosis hand congenital deformity disease
 * bone development disease characterized by short fingers and toes
 * DOID:0050581
 * C05.660.585.262 C16.131.621.585.262
 * Brachydactyly
 * Brachydaktylia.svg
 * brachydactyly type A1B
 * class of disease
 * brachydactyly type A1
 * A brachydactyly type A1 characterized by shortened middle phalanges of all the digits and shortened proximal phalanges of the thumbs and big toes but normal stature that has material basis in variation in the chromosome region 5p13.3-p13.2.
 * DOID:0110974
 * bradyopsia
 * class of disease
 * retinal disease genetic vitreous-retinal disease
 * retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes
 * DOID:0050335
 * brain angioma
 * class of disease
 * hemangioma central nervous system organ benign neoplasm encephalopathy cerebrovascular disease
 * Human disease
 * DOID:5393
 * brain cancer
 * class of disease
 * central nervous system cancer brain tumor encephalopathy cancer
 * central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain
 * DOID:1319
 * brain compression
 * class of disease
 * encephalopathy
 * Human disease
 * DOID:11457
 * brain ependymoma
 * class of disease
 * brain glioma ependymal tumor bone cancer spinal disease
 * Human disease
 * DOID:7497
 * brain germinoma
 * class of disease
 * brain cancer central nervous system germinoma germ cell cancer
 * Human disease
 * DOID:2127
 * brain glioblastoma multiforme
 * class of disease
 * brain glioma
 * Human disease
 * DOID:3073
 * brain glioma
 * class of disease
 * brain cancer glioma
 * brain cancer that has material basis in glial cells
 * DOID:0060108
 * Brain gliomas
 * brain infarction
 * class of disease
 * cerebrovascular disease brain ischemia
 * Human disease
 * DOID:3454
 * C10.228.140.300.150.477 C10.228.140.300.775.200 C14.907.253.092.477 C14.907.253.855.200 C23.550.513.355.250 C23.550.717.489.250
 * brain ischemia
 * class of disease
 * ischemia cerebrovascular disease stroke disease
 * insufficient blood flow to the brain
 * DOID:2316
 * C10.228.140.300.150 C14.907.253.092
 * Brain ischemia
 * brain meningioma
 * class of disease
 * brain cancer meningioma
 * Human disease
 * DOID:0060106
 * brain oligodendroglioma
 * class of disease
 * brain glioma oligodendroglioma
 * brain glioma that has material basis in oligodendrocytes
 * DOID:3187
 * brain sarcoma
 * class of disease
 * brain cancer central nervous system sarcoma
 * Human disease
 * DOID:2132
 * brain small vessel disease
 * class of disease
 * encephalopathy
 * human disease
 * DOID:0112313
 * brain small vessel disease 3
 * class of disease
 * brain small vessel disease autosomal recessive disease
 * human disease
 * DOID:0112315
 * brain stem angioblastoma
 * class of disease
 * brain stem cancer hemangioblastoma benign neoplasm of brain stem carcinoma
 * Human disease
 * DOID:6501
 * brain stem astrocytic neoplasm
 * class of disease
 * Brainstem glioma brain astrocytoma
 * Human disease
 * DOID:4860
 * brain stem cancer
 * class of disease
 * infratentorial cancer brain stem neoplasm
 * Human disease
 * DOID:4203
 * brain stem ependymoma
 * class of disease
 * Brainstem glioma brain ependymoma ependymal tumor
 * Human disease
 * DOID:5508
 * brain stem infarction
 * class of disease
 * brain infarction brain stem stroke syndrome
 * human disease
 * DOID:3523
 * C10.228.140.300.150.477.100 C10.228.140.300.775.200.100 C14.907.253.092.477.100 C14.907.253.855.200.100
 * brain stem medulloblastoma
 * class of disease
 * brain stem cancer medulloblastoma
 * brain stem cancer that begins in the lower part of the brain on the floor of the skull
 * DOID:0050899
 * brainstem intraparenchymal clear cell meningioma
 * class of disease
 * clear cell meningioma
 * Human disease
 * DOID:4209
 * branch retinal artery occlusion
 * class of disease
 * retinal artery occlusion
 * Human disease
 * DOID:13094
 * branchiootorenal syndrome 1
 * class of disease
 * branchiootorenal syndrome
 * human disease
 * DOID:0111423
 * branchiootorenal syndrome 2
 * class of disease
 * branchiootorenal syndrome
 * human disease
 * DOID:0111424
 * brawny scleritis
 * class of disease
 * anterior scleritis
 * Human disease
 * DOID:14287
 * breast adenocarcinoma
 * class of disease
 * breast carcinoma adenocarcinoma
 * breast carcinoma that originates in the milk ducts and/or lobules (glandular tissue) of the breast
 * DOID:3458
 * breast adenoid cystic carcinoma
 * class of disease
 * breast carcinoma breast adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:4877
 * breast adenoma
 * class of disease
 * breast benign neoplasm benign neoplasms by histologic type adenoma
 * Human disease
 * DOID:1625
 * breast adenomyoepithelial adenosis
 * class of disease
 * microglandular adenosis
 * Human disease
 * DOID:7312
 * breast adenomyoepithelioma
 * class of disease
 * breast myoepithelial neoplasm
 * breast myoepithelial neoplasm that affects the breast and is characterized by biphasic proliferation of both epithelial and myoepithelial cells
 * DOID:1642
 * breast angiomatosis
 * class of disease
 * angiomatosis capillary disease breast disease
 * Human disease
 * DOID:1637
 * breast angiosarcoma
 * class of disease
 * breast sarcoma inherited soft tissue tumor inherited gynecological tumor rare genetic vascular tumor angiosarcoma
 * angiosarcoma and sarcoma of breast and vascular neoplasm of breast that is located in the cells that line the blood vessels within the breast or underarm area
 * DOID:4511
 * breast apocrine adenoma
 * class of disease
 * breast adenoma hidradenoma benign neoplasm of sweat gland apocrine adenoma benign epithelial skin neoplasm
 * Human disease
 * DOID:7540
 * breast apocrine carcinoma
 * class of disease
 * breast adenocarcinoma apocrine adenocarcinoma
 * Human disease
 * DOID:6581
 * breast apocrine carcinoma in situ
 * class of disease
 * breast carcinoma in situ
 * Human disease
 * DOID:8428
 * breast benign neoplasm
 * class of disease symptom or sign
 * thoracic benign neoplasm breast disease breast neoplasm
 * non-metastasizing neoplasm arising from the breast parenchyma
 * DOID:0060082
 * breast cancer
 * class of disease symptom or sign
 * thoracic cancer breast disease breast neoplasm disease
 * cancer that originates in the mammary gland
 * DOID:1612
 * Breast cancer
 * Breast DCIS histopathology (1).jpg
 * breast capillary hemangioma
 * class of disease
 * breast hemangioma
 * Human disease
 * DOID:6491
 * breast carcinoma
 * class of disease
 * breast cancer
 * A breast cancer that has material basis in abnormally proliferating cells derives from epithelial cells.
 * DOID:3459
 * Breast carcinomas
 * breast carcinoma in situ
 * class of disease
 * in situ carcinoma carcinoma in situ of breast and genitourinary system breast disease
 * Human disease
 * DOID:8791
 * C04.557.470.200.240.187 C04.588.180.130 C17.800.090.500.130
 * breast columnar cell mucinous carcinoma
 * class of disease
 * breast mucinous carcinoma
 * Human disease
 * DOID:8130
 * breast cystic hypersecretory carcinoma
 * class of disease
 * breast secretory carcinoma
 * Human disease
 * DOID:7537
 * breast disease
 * class of disease
 * thoracic disease disease
 * thoracic disease that is located in the breast
 * DOID:3463
 * C17.800.090
 * Diseases and disorders of the breast
 * breast duct papilloma
 * class of disease
 * intraductal papillary breast neoplasm papilloma
 * Human disease
 * DOID:1626
 * breast ductal adenoma
 * class of disease
 * breast adenoma
 * Human disease
 * DOID:7538 DOID:5397
 * breast ductal carcinoma
 * class of disease
 * breast carcinoma ductal carcinoma
 * breast carcinoma that derives from the lining of milk ducts
 * DOID:3007
 * C04.557.470.200.025.232.500 C04.557.470.615.132.500 C04.588.180.390 C17.800.090.500.390
 * Breast ductal carcinomas
 * breast epithelioid hemangioma
 * class of disease
 * breast hemangioma histiocytoid hemangioma
 * Human disease
 * DOID:6492
 * breast fibroadenoma
 * class of disease
 * breast benign neoplasm adenoma disease
 * breast benign neoplasm comprised of fibrous and glandular tissues
 * DOID:1618
 * C04.557.450.565.590.595.350 C04.557.470.625.350
 * Breast fibroadenomas
 * Breast fibradenoma (1).jpg
 * breast fibrocystic disease
 * class of disease symptom or sign
 * breast benign neoplasm benign mammary dysplasia
 * Human disease
 * DOID:10354
 * C17.800.090.750
 * Fibrocystic breast changes
 * breast fibrosarcoma
 * class of disease
 * breast sarcoma fibrosarcoma
 * Human disease
 * DOID:6001
 * breast giant fibroadenoma
 * class of disease
 * breast fibroadenoma
 * Human disease
 * DOID:7223
 * breast granular cell tumor
 * class of disease
 * breast cancer
 * Human disease
 * DOID:3011
 * breast hemangioma
 * class of disease
 * breast benign neoplasm hemangioma
 * Human disease
 * DOID:476
 * breast hemangiopericytoma
 * class of disease
 * breast sarcoma hemangiopericytoma
 * hemangiopericytoma that is manifested in the breast
 * DOID:5370
 * breast implant-associated anaplastic large cell lymphoma
 * class of disease
 * peripheral T-cell lymphoma
 * human disease
 * DOID:0070333
 * breast intracanalicular fibroadenoma
 * class of disease
 * breast fibroadenoma
 * Human disease
 * DOID:2656
 * breast intraductal papillomatosis
 * class of disease
 * breast papillomatosis intraductal papillomatosis intraductal breast papilloma
 * Human disease
 * DOID:7511
 * breast intraductal proliferative lesion
 * class of disease
 * intraductal breast neoplasm
 * Human disease
 * DOID:6839
 * breast juvenile papillomatosis
 * class of disease
 * breast papillomatosis
 * Human disease
 * DOID:6641
 * breast large cell neuroendocrine carcinoma
 * class of disease
 * inherited gynecological tumor rare genetic respiratory disease inherited neuroendocrine tumor invasive breast carcinoma breast carcinoma
 * Human disease
 * DOID:6657
 * breast leiomyoma
 * class of disease
 * breast benign neoplasm leiomyoma
 * Human disease
 * DOID:1623
 * breast leiomyosarcoma
 * class of disease
 * breast sarcoma inherited gynecological tumor inherited soft tissue tumor
 * Human disease
 * DOID:5285
 * breast liposarcoma
 * class of disease
 * breast sarcoma
 * Human disease
 * DOID:5701
 * breast lobular carcinoma
 * class of disease
 * breast carcinoma Lobular carcinoma
 * breast carcinoma that derives from breast lobules (milk glands)
 * DOID:0050938
 * C04.557.470.200.025.305 C04.557.470.615.305 C04.588.180.437 C17.800.090.500.437
 * breast lymphoma
 * class of disease
 * breast cancer inherited gynecological tumor genetic hematologic disease lymphoma
 * Human disease
 * DOID:5826
 * breast malignant eccrine spiradenoma
 * class of disease
 * breast cancer inherited gynecological tumor inherited skin tumor genetic epidermal disorder malignant spiradenoma breast adenocarcinoma
 * Human disease
 * DOID:7983
 * breast malignant phyllodes tumor
 * class of disease
 * breast cancer breast fibroepithelial neoplasm phyllodes tumor malignant phyllodes tumor
 * Human disease
 * DOID:3016
 * breast medullary carcinoma
 * class of disease
 * breast adenocarcinoma invasive ductal carcinoma
 * Human disease
 * DOID:5605
 * breast metaplastic carcinoma
 * class of disease
 * breast carcinoma Metaplastic carcinoma invasive breast carcinoma
 * Human disease
 * DOID:4680
 * breast mucinous carcinoma
 * class of disease
 * breast adenocarcinoma invasive ductal carcinoma
 * Human disease
 * DOID:3610
 * Mucinous breast carcinoma
 * breast mucinous cystadenocarcinoma
 * class of disease
 * breast mucinous carcinoma mucinous cystadenocarcinoma
 * Human disease
 * DOID:3609
 * breast mucoepidermoid carcinoma
 * class of disease
 * breast metaplastic carcinoma breast adenocarcinoma mucoepidermoid carcinoma
 * Human disease
 * DOID:4679
 * breast myoepithelial carcinoma
 * class of disease
 * breast carcinoma invasive breast carcinoma myoepithelial carcinoma
 * Human disease
 * DOID:6776
 * breast myoepithelial neoplasm
 * class of disease
 * breast cancer
 * Human disease
 * DOID:3004
 * breast myoepitheliosis
 * class of disease
 * breast myoepithelial neoplasm
 * Human disease
 * DOID:7521
 * breast neuroendocrine neoplasm
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:3009
 * breast osteosarcoma
 * class of disease
 * breast sarcoma extraosseous osteosarcoma
 * Human disease
 * DOID:7787
 * breast papillary carcinoma
 * class of disease
 * breast carcinoma breast papillary neoplasm
 * Human disease
 * DOID:5592
 * breast papillomatosis
 * class of disease
 * breast benign neoplasm papillomatosis
 * Human disease
 * DOID:1634
 * breast pericanalicular fibroadenoma
 * class of disease
 * breast fibroadenoma
 * Human disease
 * DOID:2639
 * breast rhabdomyosarcoma
 * class of disease
 * breast sarcoma
 * Human disease
 * DOID:4060
 * breast sarcoma
 * class of disease
 * breast cancer
 * breast cancer that has material basis in abnormally proliferating cells derives from mesenchymal cells
 * DOID:3017
 * breast scirrhous carcinoma
 * class of disease
 * breast carcinoma invasive ductal carcinoma
 * Human disease
 * DOID:7578
 * breast secretory carcinoma
 * class of disease
 * breast adenocarcinoma invasive ductal carcinoma secretory carcinoma
 * Human disease
 * DOID:4922
 * breast signet ring cell adenocarcinoma
 * class of disease
 * breast adenocarcinoma signet ring cell adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:3503
 * breast squamous cell carcinoma
 * class of disease
 * breast metaplastic carcinoma squamous cell carcinoma
 * Human disease
 * DOID:5514
 * brittle cornea syndrome 2
 * class of disease
 * autosomal recessive disease corneal disease Ehlers-Danlos syndrome
 * human disease
 * DOID:0080729
 * broad ligament malignant neoplasm
 * class of disease
 * uterine adnexa cancer
 * Human disease
 * DOID:10744
 * bronchial mucus gland adenoma
 * class of disease
 * bronchus adenoma
 * Human disease
 * DOID:7030
 * bronchial neoplasm
 * class of disease
 * respiratory system benign neoplasm bronchospasm
 * human disease
 * DOID:3906
 * C04.588.894.797.520.109 C08.127.265 C08.785.520.100
 * bronchiectasis 1
 * class of disease
 * bronchiectasis autosomal dominant disease
 * bronchiectasis that has material basis in mutation in the gene encoding the beta subunit of the epithelial sodium channel on chromosome 16p12
 * DOID:0080526
 * bronchiectasis 2
 * class of disease
 * autosomal dominant disease bronchiectasis
 * bronchiectasis that has material basis in mutation in the gene encoding the alpha subunit of the epithelial sodium channel
 * DOID:0080527
 * bronchiectasis 3
 * class of disease
 * autosomal dominant disease bronchiectasis
 * bronchiectasis that has material basis in mutation in the gene encoding the gamma subunit of the epithelial sodium channel
 * DOID:0080528
 * bronchiolitis
 * class of disease symptom or sign
 * lung disease bronchospasm respiratory syncytial virus infectious disease respiratory signs and symptoms disease
 * blockage of the small airways in the lungs due to a viral infection
 * DOID:2942
 * C08.127.446.135 C08.381.495.146.135 C08.730.099.135 C01.748.099.135
 * Bronchiolitis
 * Bronchiolitis chest X-ray.jpg
 * bronchiolo-alveolar adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * lung adenocarcinoma characterized by a predominantly lepidic pattern and 5 mm or less invasion in greatest dimension
 * DOID:4926
 * C04.557.470.200.025.022.500 C04.588.894.797.520.055.500
 * Bronchiolo-alveolar carcinoma
 * bronchitis
 * class of disease symptom or sign
 * bronchospasm chronic obstructive pulmonary disease respiratory signs and symptoms disease
 * inflammation of the large airways in the lungs
 * DOID:6132
 * C08.127.446 C08.381.495.146 C08.730.099
 * Bronchitis
 * Acute-bronchitis.jpg
 * bronchospasm
 * class of disease
 * lower respiratory tract disease bronchial disease disease
 * lower respiratory tract disease that affects the airways leading into the lungs
 * DOID:1176
 * C08.127.321
 * bronchus adenoma
 * class of disease
 * lung adenoma bronchial neoplasm respiratory tract papilloma benign neoplasms by histologic type adenoma
 * Human disease
 * DOID:5391
 * bronchus cancer
 * class of disease
 * respiratory system cancer lung cancer bronchospasm
 * respiratory system cancer that is located in the bronchus
 * DOID:1325
 * bronchus carcinoma
 * class of disease
 * bronchus cancer carcinoma
 * bronchus cancer that has material basis in epithelial cells
 * DOID:3904
 * C04.588.894.797.520.109.220 C08.381.540.140 C08.785.520.100.220
 * brown shrimp allergy
 * class of disease
 * shrimp allergy crustacean allergy
 * crustacean allergy triggered by Farfantepenaeus aztecus
 * DOID:0060525
 * bruxism
 * class of disease symptom or sign
 * sleep disorder parafunctional habit disease
 * disorder that involves involuntarily grinding or clenching of the teeth
 * DOID:2846
 * C07.793.099
 * Bruxism
 * Deviated midline 2.JPG
 * bubonic plague
 * class of disease
 * plague lymph node disease disease
 * human and animal disease
 * DOID:10773
 * Bubonic plague
 * Yersinia pestis.jpg
 * bulbomembranous urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8259
 * bulbospinal polio
 * class of disease
 * paralytic poliomyelitis spinal cord disease
 * Human disease
 * DOID:0050514
 * bullous keratopathy
 * class of disease
 * corneal edema keratopathy cornea blistering
 * Human disease
 * DOID:11031
 * bullous pemphigoid
 * class of disease
 * autoimmune skin disease pemphigoid bullous skin disease disease
 * autoimmune disease of skin and connective tissue characterized by large blisters
 * DOID:8506
 * C17.800.865.690 C20.111.730
 * Bullous pemphigoid
 * Bullous pemphgoid in a 72 year old bedridden female2.JPG
 * bullous retinoschisis
 * class of disease
 * retinoschisis
 * Human disease
 * DOID:12108
 * bullous skin disease
 * class of disease
 * dermatitis cellulitis autoimmune skin disease connective tissue disease
 * An autoimmune disease of skin and connective tissue that is characterized by blisters filled with a watery fluid, located in skin. The disease is associated with the amount of gluten ingested.
 * DOID:8502
 * buphthalmos
 * class of disease
 * hydrophthalmos disease
 * Human disease
 * DOID:11211
 * Buphthalmos
 * burning mouth syndrome
 * class of disease symptom or sign
 * mouth disease dysesthesia glossalgia rare headache disorder burning sensation disease
 * Human disease
 * DOID:4331
 * C07.465.114
 * Burning mouth syndrome
 * bursitis
 * class of disease symptom or sign
 * arthropathy synovial, tendon or bursa disorder inflammation disease
 * human disease
 * DOID:2965
 * C05.550.251
 * Bursitis
 * Bursitis Elbow WC.JPG
 * byssinosis
 * class of disease
 * pneumoconiosis disease
 * human disease of the respiratory system
 * DOID:10323
 * C08.381.483.581.275 C24.800.323 C08.381.520.702.275
 * calcaneal spur
 * class of disease
 * osteophyte foot diseases exostosis
 * exostosis that results in an abnomal growth located in calcaneus
 * DOID:210
 * C05.116.540.310.600 C05.360.400
 * Calcaneal spur
 * 2023 Ostroga piętowa.jpg
 * calcaneonavicular coalition
 * class of disease
 * synostosis tarsal-carpal coalition syndrome
 * synostosis characterized by the fusion of carpal and tarsal bones, which causes stiffness and immobility of the hands and the feet
 * DOID:14762
 * calcific tendinitis
 * class of disease
 * tendinitis calcium deposits in tendon and bursa
 * disorder characterized by deposits of hydroxyapatite (a crystalline calcium phosphate) in any tendon of the body
 * DOID:14181
 * Calcific tendinitis
 * calcinosis
 * class of disease
 * calcium metabolism disease ectopic calcification disease
 * calcium metabolism disease that is the result of the formation of calcium deposits in any soft tissue
 * DOID:182
 * C18.452.174.130
 * Calcinosis
 * calciphylaxis
 * class of disease
 * calcinosis systemic disease vascular disease
 * Human disease
 * DOID:4734
 * C18.452.174.130.186
 * Calciphylaxis
 * Calciphylaxis.png
 * calcium metabolism disease
 * class of disease
 * mineral metabolism disease
 * Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization
 * DOID:10575
 * C18.452.174
 * Ca-TableImage.svg
 * calcium oxalate nephrolithiasis
 * class of disease
 * nephrolithiasis
 * human disease
 * DOID:0080652
 * cancer
 * class of disease
 * disease of cellular proliferation neoplasm tumor disease
 * group of diseases involving abnormal cell growth and spread
 * DOID:162
 * Breast cancer cell (2).jpg
 * cancer of exocrine pancreas
 * class of disease
 * pancreatic cancer pancreatic exocrine neoplasm
 * Human disease
 * DOID:1795
 * cancerophobia
 * class of disease
 * nosophobia
 * overwhelming, irrational, and persistent fear of being diagnosed with cancer
 * DOID:602
 * candidal paronychia
 * class of disease
 * candidiasis paronychia nail disease
 * Human disease
 * DOID:14512
 * cannabis abuse
 * class of disease
 * substance abuse effects of cannabis cannabis consumption
 * substance abuse that involves the recurring use of cannabis despite negative consequences
 * DOID:9505
 * C25.775.635 F03.900.635
 * cannabis dependence
 * class of disease
 * hallucinogen dependence effects of cannabis
 * drug dependence that involves the continued use of cannabis despite problems related to use of the substance
 * DOID:1849
 * capillariasis
 * class of disease
 * parasitic helminthiasis infectious disease intestinal disease liver disease lung disease disease
 * disease caused by nematodes of the genus Capillaria
 * DOID:12474
 * capillary disease
 * class of disease
 * vascular disease microangiopathy
 * vascular disease that is located in the capillaries
 * DOID:1271
 * capillary hemangioma
 * class of disease symptom or sign
 * capillary disease skin hemangioma
 * most common variant of hemangioma, dull red, firm, dome-shaped hemangioma, usually located on the head and neck, which grows rapidly caused by proliferation of immature capillary vessels
 * DOID:2725
 * C04.557.645.375.380
 * Cutaneous capillary hemangioma
 * Capillary haemangioma.jpg
 * capillary leak syndrome
 * class of disease
 * capillary disease urticarial syndrome disease
 * human disease
 * DOID:14400
 * C14.907.218
 * capillary lymphangioma
 * class of disease
 * capillary disease lymphangioma
 * Human disease
 * DOID:2286
 * carbamazepine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger carbamazepine
 * DOID:0040006
 * carbapenem allergy
 * class of disease
 * drug allergy beta-lactam allergy
 * drug allergy that has allergic trigger carbapenems
 * DOID:0040032
 * carbohydrate metabolic disorder
 * class of disease
 * inherited metabolic disorder carbohydrate metabolism disease
 * inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates
 * DOID:2978
 * C16.320.565.202 C18.452.648.202
 * Disorders of carbohydrate metabolism
 * carbohydrate metabolism disease
 * class of disease
 * acquired metabolic disease
 * acquired metabolic disease that is characterized by abnormal carbohydrate metabolism
 * DOID:0050013
 * carbuncle
 * class of disease гнійне захворювання
 * pyoderma
 * human disease
 * DOID:2176
 * C01.150.252.410.868.951.270.200 C01.150.252.819.770.270.200 C01.800.720.770.270.200 C17.800.838.765.770.270.200
 * Carbuncles
 * Carbuncle on buttok.JPG
 * carcinoma of supraglottis
 * class of disease
 * supraglottis cancer
 * Human disease
 * DOID:7763
 * carcinosarcoma
 * class of disease
 * malignant mixed tumor disease
 * mixed cell type cancer that has material basis in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components
 * DOID:4236
 * C04.557.435.290 C04.557.450.795.290
 * Carcinosarcoma
 * cardia cancer
 * class of disease
 * stomach cancer
 * human disease
 * DOID:10548
 * cardiac granular cell neoplasm
 * class of disease
 * cardiovascular organ benign neoplasm benign neoplasm of epicardium
 * Human disease
 * DOID:5044
 * cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
 * class of disease
 * genetic disease genetic syndromic intellectual disability rare syndrome with cardiac malformations syndrome autosomal dominant disease
 * human disease
 * DOID:0111697
 * cardiac sarcoidosis
 * class of disease
 * sarcoidosis heart disease
 * Human disease
 * DOID:13405
 * cardiac tuberculosis
 * class of disease
 * cardiovascular tuberculosis heart disease
 * human disease
 * DOID:0060570
 * cardiac valvular defect, developmental
 * class of disease
 * genetic disease congenital disorder Heart valve dysplasia
 * human disease
 * DOID:0080633
 * cardiofaciocutaneous syndrome 1
 * class of disease
 * autosomal dominant disease cardiofaciocutaneous syndrome
 * human disease
 * DOID:0111460
 * cardiofaciocutaneous syndrome 2
 * class of disease
 * autosomal dominant disease cardiofaciocutaneous syndrome
 * human disease
 * DOID:0111461
 * cardiofaciocutaneous syndrome 3
 * class of disease
 * cardiofaciocutaneous syndrome autosomal dominant disease
 * human disease
 * DOID:0111462
 * cardiofaciocutaneous syndrome 4
 * class of disease
 * cardiofaciocutaneous syndrome autosomal dominant disease
 * human disease
 * DOID:0111463
 * cardiomyopathy, infantile hypertrophic
 * class of disease
 * genetic disease hypertrophic cardiomyopathy
 * human disease
 * DOID:0111753
 * cardiovascular organ benign neoplasm
 * class of disease
 * organ system benign neoplasm cardiovascular neoplasm cardiovascular disease
 * organ system benign neoplasm disease located in the blood, heart, blood vessels or the lymphatic system
 * DOID:0060091
 * carotenemia
 * class of disease
 * acquired metabolic disease
 * Human disease
 * DOID:9969
 * carotid artery disease
 * class of disease
 * cerebrovascular disease artery disease
 * human disease
 * DOID:3407
 * C10.228.140.300.200 C14.907.253.123
 * carotid artery dissection
 * class of disease
 * carotid artery disease dissection disease
 * Human disease
 * DOID:9348
 * Gray513.png
 * carotid artery occlusion
 * class of disease
 * occlusion precerebral artery carotid artery stenosis carotid artery disease Vascular occlusion
 * human disease
 * DOID:807
 * carotid artery stenosis
 * class of disease
 * carotid artery disease peripheral artery disease
 * narrowing or constriction of the inner surface (lumen) of the carotid artery, usually caused by atherosclerosis
 * DOID:13001
 * C10.228.140.300.200.360 C14.907.137.230 C14.907.253.123.360
 * Carotid artery stenosis
 * Gray513.png
 * carotid artery thrombosis
 * class of disease
 * carotid artery disease intracranial thrombosis
 * Human disease
 * DOID:3410
 * C10.228.140.300.200.355 C14.907.253.123.355 C14.907.253.566.206 C14.907.355.590.213.206
 * carp allergy
 * class of disease
 * fish allergy
 * fish allergy triggered by Cyprinus carpio
 * DOID:0060516
 * cartilage cancer
 * class of disease
 * connective tissue neoplasm chondropathy cartilage tumor
 * Human disease
 * DOID:0060102
 * carvone allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger (-)-carvone
 * DOID:0040064
 * cascade stomach
 * class of disease
 * stomach disease
 * Human disease
 * DOID:12234
 * cataract 1 multiple types
 * class of disease
 * cataract autosomal dominant disease
 * cataract that has material basis in heterozygous mutation in the gene encoding the alpha-8 subunit of the gap junction protein (GJA8) on chromosome 1q21
 * DOID:0110231
 * cataract 24
 * class of disease
 * cataract autosomal dominant disease
 * cataract that has material basis in variation in the region 17p13
 * DOID:0110257
 * cataract 26 multiple types
 * class of disease
 * cataract
 * cataract that has material basis in variation in the region 9q13-q22
 * DOID:0110246
 * cataract 27
 * class of disease
 * cataract
 * cataract that has material basis in mutation in the region 2p12
 * DOID:0110233
 * cataract 28
 * class of disease
 * cataract
 * human disease
 * DOID:0110244
 * cataract 29
 * class of disease
 * cataract autosomal dominant disease
 * cataract that has material basis in variation in the region 2pter-p24
 * DOID:0110232
 * cataract 3 multiple types
 * class of disease
 * cataract autosomal dominant disease
 * cataract that has material basis in heterozygous mutation in the beta-B2-crystallin gene (CRYBB2) on chromosome 22q11
 * DOID:0110269
 * cataract 37
 * class of disease
 * cataract autosomal dominant disease
 * A cataract that has material basis in variation in the region 12q24.2-q24.3.
 * DOID:0110252
 * cataract 4 multiple types
 * class of disease
 * cataract autosomal dominant disease
 * cataract that has material basis in heterozygous mutation in the gamma-D-crystallin gene (CRYGD) on chromosome 2q33
 * DOID:0110234
 * cataract 47
 * class of disease
 * autosomal dominant disease cataract
 * human disease
 * DOID:0070353
 * cataract 48
 * class of disease
 * cataract autosomal recessive disease
 * human disease
 * DOID:0070354
 * cataract 9 multiple types
 * class of disease
 * cataract autosomal recessive disease autosomal dominant disease
 * cataract that has material basis in heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22
 * DOID:0110266
 * catecholaminergic polymorphic ventricular tachycardia 1
 * class of disease
 * catecholaminergic polymorphic ventricular tachycardia
 * catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has material basis in heterozygous mutation in the RYR2 gene on chromosome 1q43
 * DOID:0060675
 * cauda equina intradural extramedullary astrocytoma
 * class of disease
 * cauda equina neoplasm
 * Human disease
 * DOID:4846
 * cauda equina neoplasm
 * class of disease
 * spinal cord neoplasm nerve root neoplasm
 * Human disease
 * DOID:4847
 * cauda equina syndrome
 * class of disease
 * peripheral neuropathy syndrome disease
 * nerve damage at the end of the spinal cord
 * DOID:11577
 * C10.668.829.550.350 C10.668.829.800.750.150
 * Cauda equina syndrome
 * [[File:MRI of the lumbar spine with abscess in the posterior epidural space, causing cauda equina syndrome.jpg|center|64px]]
 * causalgia
 * class of disease
 * complex regional pain syndrome
 * human disease
 * DOID:3222
 * C10.177.195.200 C10.668.829.250.200 C10.668.829.600.200
 * cavernous hemangioma
 * class of disease symptom or sign
 * vascular hemostatic disease disease
 * human disease
 * DOID:483
 * C04.557.645.375.385 C14.907.454.385 C15.378.463.515.385
 * Cavernous hemangiomas
 * cavernous hemangioma of orbit
 * class of disease
 * cavernous hemangioma hemangioma of orbit
 * Human disease
 * DOID:14463
 * cavernous sinus thrombosis
 * class of disease
 * cerebral venous sinus thrombosis disease
 * Human disease
 * DOID:3575
 * C10.228.140.300.525.425.500.375 C14.907.253.566.350.500.375 C14.907.355.590.213.350.500.375
 * Gray571.png
 * cecal disease
 * class of disease
 * intestinal disease
 * intestinal disease located in the cecum
 * DOID:1518
 * C06.405.469.110
 * cecum adenoma
 * class of disease
 * cecal benign neoplasm benign neoplasms by histologic type adenoma
 * cecal benign neoplasm that has material basis in epithelial tissue with glandular origin
 * DOID:0050910
 * cecum cancer
 * class of disease
 * large intestine cancer cecal neoplasm cecal disease
 * large intestine cancer that is located in the cecum
 * DOID:1521
 * cecum lymphoma
 * class of disease
 * cecum cancer lymphoma
 * human disease
 * DOID:1522
 * cefaclor allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger cefaclor
 * DOID:0040023
 * cefixime allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger cefixime
 * DOID:0040030
 * cefotaxime allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger cefotaxime
 * DOID:0040020
 * cefotiam allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger cefotiam
 * DOID:0040103
 * ceftazidime allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger ceftazidime
 * DOID:0040024
 * ceftriaxone allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger ceftriaxone
 * DOID:0040005
 * cefuroxime allergy
 * class of disease
 * cephalosporin allergy
 * cephalosporin allergy that has allergic trigger cefuroxime
 * DOID:0040025
 * celery allergy
 * class of disease
 * vegetable allergy
 * human disease
 * DOID:0070335
 * celiac disease
 * class of disease symptom or sign
 * autoimmune disease of gastrointestinal tract gluten-related disorder disease
 * long term autoimmune disorder caused by a reaction to gluten
 * DOID:10608
 * C06.405.469.637.250 C18.452.603.250
 * Coeliac disease
 * Coeliac path.jpg
 * cell type cancer
 * class of disease
 * cancer
 * cancer that is classified by the type of cell from which it is derived
 * DOID:0050687
 * Cancers by histological type
 * cellular congenital mesoblastic nephroma
 * class of disease
 * congenital mesoblastic nephroma
 * Human disease
 * DOID:8082
 * cellular ependymoma
 * class of disease
 * benign ependymoma
 * An ependymoma which shows conspicuous cellularity without a significant increase in mitotic rate. (Adapted from WHO)
 * DOID:5500
 * cellular leiomyoma
 * class of disease
 * leiomyoma
 * Human disease
 * DOID:5139
 * cellular myxoid liposarcoma
 * class of disease
 * liposarcoma myxoid liposarcoma
 * Human disease
 * DOID:5692
 * cellular neurofibroma
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:5152
 * cellular phase chronic idiopathic myelofibrosis
 * class of disease
 * myelofibrosis chronic idiopathic myelofibrosis
 * Human disease
 * DOID:8106
 * cellular schwannoma
 * class of disease
 * neurilemmoma
 * neurilemmoma with a predominantly cellular growth but no Verocay bodies
 * DOID:3196
 * central breast papilloma
 * class of disease
 * breast duct papilloma
 * Human disease
 * DOID:8224
 * central conducting lymphatic anomaly
 * class of disease
 * lymphatic system disease autosomal dominant disease
 * human disease
 * DOID:0081030
 * central corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:9910
 * central epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma
 * Human disease
 * DOID:7492
 * central gyrate choroidal dystrophy
 * class of disease
 * partial central choroid dystrophy
 * human disease
 * DOID:9820
 * central nervous system adult germ cell tumor
 * class of disease
 * central nervous system germ cell tumor
 * Human disease
 * DOID:5349
 * central nervous system angiosarcoma
 * class of disease
 * central nervous system sarcoma
 * central nervous system sarcoma that is located in the inner lining of blood vessels
 * DOID:4504
 * central nervous system cancer
 * class of disease
 * nervous system cancer central nervous system neoplasm central nervous system disease
 * nervous system cancer that is located in the central nervous system
 * DOID:3620
 * central nervous system childhood germ cell tumor
 * class of disease
 * central nervous system germ cell tumor germ cell cancer pediatric germ cell tumor
 * Human disease
 * DOID:6052
 * central nervous system chondroma
 * class of disease
 * chondroma central nervous system organ benign neoplasm soft tissue chondroma
 * Human disease
 * DOID:3813
 * central nervous system disease
 * class of disease
 * neurological disorder nervous system disease
 * nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system
 * DOID:331
 * C10.228
 * Diseases and disorders of the central nervous system
 * central nervous system embryonal carcinoma
 * class of disease
 * central nervous system germ cell tumor embryonal carcinoma primary germ cell tumor of central nervous system
 * Human disease
 * DOID:7232
 * central nervous system endodermal sinus tumor
 * class of disease
 * central nervous system germ cell tumor malignant mixed tumor sarcoma germ cell cancer primary germ cell tumor of central nervous system
 * Human disease
 * DOID:5343
 * central nervous system fibrosarcoma
 * class of disease
 * central nervous system sarcoma fibrosarcoma
 * Human disease
 * DOID:6451
 * central nervous system germ cell tumor
 * class of disease
 * central nervous system cancer extragonadal germ cell tumor germ cell cancer
 * Human disease
 * DOID:4439
 * central nervous system germinoma
 * class of disease
 * central nervous system germ cell tumor germinoma germ cell cancer
 * Human disease
 * DOID:4438
 * central nervous system hemangioma
 * class of disease
 * hemangioma central nervous system organ benign neoplasm
 * hemangioma arising from the brain and spinal cord
 * DOID:501
 * central nervous system hematologic cancer
 * class of disease
 * central nervous system cancer hematologic cancer
 * hematologic cancer and central nervous system neoplasm that is located in the central nervous system
 * DOID:5772
 * central nervous system immature teratoma
 * class of disease
 * central nervous system teratoma
 * Human disease
 * DOID:6019
 * central nervous system leiomyoma
 * class of disease
 * central nervous system organ benign neoplasm leiomyoma
 * Human disease
 * DOID:5126
 * central nervous system leiomyosarcoma
 * class of disease
 * central nervous system mesenchymal non-meningothelial tumor leiomyosarcoma malignant central nervous system mesenchymal, non-meningothelial neoplasm
 * Human disease
 * DOID:5254
 * central nervous system leukemia
 * class of disease
 * leukemia central nervous system hematologic cancer central nervous system cancer
 * hematologic cancer located in the central nervous system
 * DOID:12969
 * central nervous system lipoma
 * class of disease
 * central nervous system organ benign neoplasm lipoma
 * human disease
 * DOID:6293
 * central nervous system lymphoma
 * class of disease
 * lymphoma central nervous system hematologic cancer
 * hematologic cancer that has material basis in lymphoma located in central nervous system
 * DOID:3234
 * central nervous system mature teratoma
 * class of disease
 * central nervous system teratoma mature teratoma
 * Human disease
 * DOID:6017
 * central nervous system melanocytic neoplasm
 * class of disease
 * central nervous system neoplasm melanocytic tumor central nervous system cancer
 * Human disease
 * DOID:4955
 * central nervous system organ benign neoplasm
 * class of disease
 * nervous system benign neoplasm central nervous system neoplasm central nervous system disease
 * Human disease
 * DOID:0060090
 * central nervous system origin vertigo
 * class of disease
 * central nervous system disease encephalopathy vertigo
 * Human disease
 * DOID:2479
 * central nervous system osteosarcoma
 * class of disease
 * central nervous system mesenchymal non-meningothelial tumor extraosseous osteosarcoma malignant central nervous system mesenchymal, non-meningothelial neoplasm
 * Human disease
 * DOID:7994
 * central nervous system primitive neuroectodermal neoplasm
 * class of disease
 * central nervous system cancer neuroectodermal tumor Embryonal tumors of the central nervous system primitive neuroectodermal tumor
 * Human disease
 * DOID:0060103
 * Primitive neuroectodermal tumor
 * central nervous system rhabdomyosarcoma
 * class of disease
 * central nervous system sarcoma rhabdomyosarcoma nervous system cancer central nervous system disease
 * Human disease
 * DOID:4048
 * central nervous system sarcoma
 * class of disease
 * central nervous system cancer sarcoma
 * human disease
 * DOID:2133
 * central nervous system teratoma
 * class of disease
 * central nervous system germ cell tumor primary germ cell tumor of central nervous system sarcoma germ cell cancer
 * Human disease
 * DOID:3640
 * central nervous system vasculitis
 * class of disease
 * vasculitis central nervous system disease disease
 * Human disease
 * DOID:525
 * C10.114.875 C10.228.140.300.850 C14.907.253.946 C14.907.940.907 C20.111.258.962
 * central neurocytoma
 * class of disease
 * neurocytoma cerebral ventricle cancer
 * Human disease
 * DOID:14174
 * Central neurocytoma
 * central pontine myelinolysis
 * class of disease
 * demyelinating disease demyelinating disease of central nervous system
 * demyelination disease that is characterized by severe damage to the myelin sheath of the pons&#39; nerve cells and has symptom acute paralysis, has symptom dysphagia, and has symptom dysarthria
 * DOID:636
 * C10.228.140.163.560 C10.314.500 C18.452.132.560
 * Central pontine myelinolysis
 * Illu pituitary pineal glands.jpg
 * central precocious puberty
 * class of disease
 * endocrine system disease
 * human disease
 * DOID:0112308
 * central precocious puberty 1
 * class of disease
 * autosomal dominant disease
 * human disease
 * DOID:0112310
 * central pterygium
 * class of disease
 * progressive peripheral pterygium
 * Human disease
 * DOID:13473
 * central retinal artery occlusion
 * class of disease
 * retinal artery occlusion
 * retinal artery occlusion characterized by blockage of blood flow through the central retinal artery
 * DOID:13098
 * Central retinal artery occlusion
 * central retinal vein occlusion
 * class of disease
 * retinal vein occlusion
 * Human disease
 * DOID:2450
 * central sleep apnea
 * class of disease
 * sleep apnea
 * sleep apnea that is characterized by a malfunction of the basic neurological controls for breathing rate and the failure to give the signal to inhale, causing the individual to miss one or more cycles of breathing
 * DOID:9220
 * C08.618.085.852.800 C10.886.425.800.750.800
 * centronuclear myopathy 1
 * class of disease
 * An autosomal dominant centronuclear myopathy characterized by slowly progressive muscle wasting and weakness involving mainly the limb girdle, trunk, and neck muscles that has material basis in heterozygous mutation in DNM2 on 19p13.2.
 * DOID:0111223
 * centronuclear myopathy 2
 * class of disease
 * centronuclear myopathy autosomal recessive centronuclear myopathy
 * An autosomal recessive centronuclear myopathy that has material basis in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.
 * DOID:0111220
 * centronuclear myopathy 4
 * class of disease
 * autosomal dominant centronuclear myopathy
 * An autosomal dominant centronuclear myopathy that has material basis in heterozygous mutation in CCDC78 on 16p13.3.
 * DOID:0111224
 * centronuclear myopathy 5
 * class of disease
 * autosomal recessive centronuclear myopathy
 * autosomal recessive centronuclear myopathy characterized by severe neonatal hypotonia, respiratory insufficiency, and difficulty feeding that has material basis in homozygous or compound heterozygous mutation in SPEG on 2q35
 * DOID:0111222
 * centronuclear myopathy 6 with fiber-type disproportion
 * class of disease
 * congenital fiber-type disproportion
 * A congenital fiber-type disproportion characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that has material basis in homozygous or compound heterozygous mutation in ZAK on 2q31.1.
 * DOID:0111221
 * centronuclear myopathy X-linked
 * class of disease
 * centronuclear myopathy
 * centronuclear myopathy that has material basis in X-linked inheritance of mutations in MTM1 on Xq28
 * DOID:0111225
 * cephalosporin allergy
 * class of disease
 * drug allergy beta-lactam allergy
 * drug allergy that has allergic trigger cephalosporin
 * DOID:0040021
 * cercarial dermatitis
 * class of disease
 * schistosomiasis skin disease
 * human disease
 * DOID:11302
 * Schistosome cercarial dermatitis
 * Cercarial dermatitis lower legs.jpg
 * cerebellar angioblastoma
 * class of disease
 * cerebellum cancer hemangioblastoma benign neoplasm of cerebellum carcinoma
 * Human disease
 * DOID:6500
 * Cerebellar hemangioblastoma
 * cerebellar astrocytoma
 * class of disease
 * cerebellum cancer brain astrocytoma glioma
 * Human disease
 * DOID:4848
 * cerebellar ataxia
 * class of disease
 * cerebellar disease hereditary ataxia
 * cerebellar disease characterized by ataxia originating in the cerebellum.
 * DOID:0050753
 * C10.228.140.252.190 C10.597.350.090.500 C23.888.592.350.090.200
 * Cerebellar ataxia
 * cerebellar ataxia type 48
 * class of disease
 * spinocerebellar ataxia
 * human disease
 * DOID:0111746
 * cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
 * class of disease
 * syndrome neurodevelopmental disorder
 * human disease
 * DOID:0070339
 * cerebellar hypoplasia
 * class of disease
 * neurological disorder
 * rare disorder in which the cerebellum is either missing entirely or is smaller than usual
 * DOID:0070338
 * Cerebellar hypoplasia
 * cerebellar liponeurocytoma
 * class of disease
 * cerebellum cancer neuronal tumor
 * Human disease
 * DOID:6458
 * Cerebellar liponeurocytoma.jpg
 * cerebellar medulloblastoma
 * class of disease
 * cerebellum cancer medulloblastoma
 * cerebellum cancer that begins in the lower part of the brain on the floor of the skull
 * DOID:0060104
 * Cerebellar medulloblastoma (1) in adult.JPG
 * cerebellar vermis medulloblastoma
 * class of disease
 * cerebellar medulloblastoma medulloblastoma
 * Human disease
 * DOID:3860
 * cerebellopontine angle meningioma
 * class of disease
 * cerebellopontine angle tumor meningioma brain meningioma
 * Human disease
 * DOID:6337
 * cerebellopontine angle primitive neuroectodermal
 * class of disease
 * cerebellopontine angle tumor
 * Human disease
 * DOID:4787
 * cerebellopontine angle tumor
 * class of disease
 * brain stem neoplasm brain stem cancer
 * Human disease
 * DOID:3200
 * cerebellum cancer
 * class of disease
 * infratentorial cancer cerebellar disease infratentorial neoplasm
 * Human disease
 * DOID:4205
 * C04.588.614.250.195.411.211 C10.228.140.211.500.200 C10.228.140.252.200 C10.551.240.250.400.300
 * cerebral amyloid angiopathy
 * class of disease
 * amyloidosis
 * amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes
 * DOID:9246
 * C10.228.140.300.510.200.200 C14.907.253.560.200.200 C18.452.845.500.100
 * Cerebral amyloid angiopathy
 * Cerebral amyloid angiopathy - very high mag.jpg
 * cerebral angioma
 * class of disease
 * brain angioma benign neoplasm of cerebrum
 * Human disease
 * DOID:6621
 * cerebral arterial disease
 * class of disease
 * intracranial arterial disease artery disease
 * Human disease
 * DOID:3527
 * C10.228.140.300.510.200 C14.907.253.560.200
 * cerebral arteriovenous malformation
 * class of disease
 * rare genetic vascular tumor rare nervous system tumor central nervous system vascular malformation rare genetic epilepsy genetic central nervous system and retinal vascular disease central nervous system organ benign neoplasm hemangioma encephalopathy cerebrovascular disease
 * arteriovenous malformation that is located in the brain
 * DOID:0060688
 * C10.228.140.300.520 C10.500.190.500 C14.240.850.750.295 C14.240.850.875.500 C14.907.150.295 C14.907.253.560.400 C16.131.240.850.750.295 C16.131.240.850.875.500 C16.131.666.190.500
 * Cerebral arteriovenous malformation
 * cerebral arteritis
 * class of disease
 * central nervous system vasculitis cerebrovascular disease arteritis
 * Human disease
 * DOID:11390
 * cerebral artery occlusion
 * class of disease
 * cerebral infarction cerebrovascular disease
 * human disease
 * DOID:10127
 * cerebral atherosclerosis
 * class of disease
 * atherosclerosis intracranial arteriosclerosis
 * type of atherosclerosis where build-up of plaque in the blood vessels of the brain occurs
 * DOID:12720
 * cerebral cavernous angioma
 * class of disease
 * central nervous system cavernous hemangioma cerebrovascular disease
 * vascular anomaly of the central nervous system characterized by dilated blood-filled capillaries lacking structural support
 * DOID:0060669
 * cerebral cavernous malformation 1
 * class of disease
 * cerebral cavernous angioma
 * cerebral cavernous malformation that has material basis in heterozygous mutation in the KRIT1 gene on chromosome 7q21
 * DOID:0080491
 * cerebral convexity meningioma
 * class of disease
 * cerebral meningioma
 * Human disease
 * DOID:6114
 * cerebral creatine deficiency syndrome
 * class of disease
 * amino acid metabolic disorder
 * Human disease
 * DOID:0050798
 * cerebral degeneration
 * class of disease disease
 * encephalopathy neurodegeneration
 * human disease
 * DOID:1443
 * Cerebral atrophy
 * cerebral edema
 * class of disease
 * encephalopathy disease
 * human disease
 * DOID:4724
 * C10.228.140.187
 * Cerebral edema
 * Tumor Meningioma3.JPG
 * cerebral hemisphere lipoma
 * class of disease
 * central nervous system lipoma benign neoplasm of cerebrum intracranial lipoma
 * Human disease
 * DOID:6291
 * cerebral infarction
 * class of disease
 * brain infarction disease
 * type of ischemic stroke resulting from a blockage in the blood vessels supplying blood to the brain
 * DOID:3526
 * C10.228.140.300.150.477.200 C10.228.140.300.775.200.200 C14.907.253.092.477.200 C14.907.253.855.200.200 C23.550.513.355.250.200 C23.550.717.489.250.200
 * Cerebral infarction
 * Infarction.svg
 * cerebral lipidosis
 * class of disease
 * cerebral degeneration lipid storage disease encephalopathy metabolic disease with dementia
 * Human disease
 * DOID:10742
 * cerebral lymphoma
 * class of disease
 * cerebrum cancer central nervous system lymphoma lymphoma central nervous system hematologic cancer
 * cerebrum cancer that affects the lymph cells and derives from the brain
 * DOID:5815
 * cerebral malaria
 * class of disease
 * malaria
 * malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species
 * DOID:14069
 * C01.207.205.300.500 C01.610.105.300.500 C01.610.752.530.620 C01.920.875.620 C10.228.228.205.300.500
 * Cerebral malaria
 * cerebral meningioma
 * class of disease
 * cerebrum cancer meningioma
 * Human disease
 * DOID:6112
 * cerebral neuroblastoma
 * class of disease
 * brain cancer cerebrum cancer intracranial primitive neuroectodermal tumor
 * Human disease
 * DOID:4164
 * cerebral palsy
 * class of disease
 * encephalopathy cerebral degeneration palsy disease
 * group of permanent movement disorders that appear in early childhood
 * DOID:1969
 * C10.228.140.140.254
 * Cerebral palsy
 * Gray764.png
 * cerebral primitive neuroectodermal tumor
 * class of disease
 * cerebrum cancer primitive neuroectodermal tumor
 * Human disease
 * DOID:7398
 * cerebral sarcoidosis
 * class of disease
 * sarcoidosis neurosarcoidosis
 * Human disease
 * DOID:13403
 * cerebral venous sinus thrombosis
 * class of disease
 * venous thrombosis intracranial thrombosis stroke disease
 * presence of acute thrombosis (a blood clot) in the dural venous sinuses, which drain blood from the brain.
 * DOID:3572
 * C10.228.140.300.525.425.500 C14.907.253.566.350.500 C14.907.355.590.213.350.500
 * Cerebral venous sinus thrombosis
 * MBq sinusvenenthrombose.jpg
 * cerebral ventricle cancer
 * class of disease
 * cerebrum cancer cerebral ventricle neoplasm
 * cerebrum cancer that is located in the cerebral ventricles
 * DOID:3541
 * cerebritis
 * class of disease
 * encephalopathy brain inflammatory disease
 * Human disease
 * DOID:3431
 * cerebrooculofacioskeletal syndrome
 * class of disease
 * Cockayne syndrome
 * human disease
 * DOID:0080910
 * cerebrooculofacioskeletal syndrome 1
 * class of disease
 * human disease
 * DOID:0080911
 * cerebrovascular benign neoplasm
 * class of disease
 * cardiovascular organ benign neoplasm cerebrovascular disease
 * cardiovascular organ benign neoplasm that is located in the cerebrovascular system
 * DOID:60007
 * cerebrovascular disease
 * class of disease
 * central nervous system disease vascular disease encephalopathy central nervous system and retinal vascular disease disease
 * artery disease that is characterized by dysfunction of the blood vessels supplying the brain
 * DOID:6713
 * C10.228.140.300 C14.907.253
 * Cerebrovascular diseases
 * 1471-2415-12-28-1Cerebral angiogram.jpg
 * cerebrum cancer
 * class of disease
 * supratentorial cancer neoplasm of cerebral hemisphere
 * supratentorial cancer that is located in the cerebrum
 * DOID:368
 * ceruminoma
 * class of disease
 * apocrine sweat gland neoplasm ceruminous tumor apocrine adenoma
 * Human disease
 * DOID:7549
 * cervical Mullerian papilloma
 * class of disease
 * cervical benign neoplasm
 * Human disease
 * DOID:9442
 * cervical Wilms' tumor
 * class of disease
 * cervical carcinosarcoma
 * cervical carcinosarcoma is located in the cervix with morphological features resembling Wilms tumor of the kidney
 * DOID:5190
 * cervical adenocarcinoma
 * class of disease
 * cervix carcinoma adenocarcinoma
 * cervix carcinoma that derives from epithelial cells of glandular origin
 * DOID:3702
 * Adenocarcinoma of the cervix
 * cervical adenofibroma
 * class of disease
 * cervical benign neoplasm
 * Human disease
 * DOID:5476
 * cervical adenoid basal carcinoma
 * class of disease
 * cervix carcinoma
 * Human disease
 * DOID:6428
 * cervical adenoid cystic carcinoma
 * class of disease
 * cervix carcinoma adenoid cystic carcinoma of the cervix uteri
 * Human disease
 * DOID:4867
 * cervical adenoma malignum
 * class of disease
 * cervical mucinous adenocarcinoma
 * Human disease
 * DOID:6627
 * cervical adenomyoma
 * class of disease
 * adenomyoma cervical uterine cancer cervical benign neoplasm
 * Human disease
 * DOID:4995
 * cervical adenosarcoma
 * class of disease
 * cervical carcinosarcoma malignant mixed epithelial and mesenchymal tumor of cervix uteri adenosarcoma
 * cervical carcinosarcoma that is located in the cervix
 * DOID:4111
 * cervical adenosquamous carcinoma
 * class of disease
 * adenosquamous carcinoma cervical squamous cell carcinoma squamous cell carcinoma cervical uterine cancer
 * cervical carcinoma that derives from squamous cells and gland-like cells
 * DOID:5636
 * cervical alveolar soft part sarcoma
 * class of disease
 * cervical uterine cancer
 * alveolar soft part sarcoma and cervical soft tissue tumor and malignant neoplasm of cervix uteri that is located in the cervix
 * DOID:4442
 * cervical atypical polypoid adenomyoma
 * class of disease
 * cervical adenomyoma
 * Human disease
 * DOID:8179
 * cervical basaloid squamous cell carcinoma
 * class of disease
 * cervical squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7046
 * cervical benign neoplasm
 * class of disease
 * uterine benign neoplasm cervix disease uterine cervix neoplasm
 * Human disease
 * DOID:0060110
 * cervical carcinosarcoma
 * class of disease
 * cervical uterine cancer malignant mixed epithelial and mesenchymal tumor of cervix uteri
 * Human disease
 * DOID:4112
 * cervical clear cell adenocarcinoma
 * class of disease
 * cervical adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5303
 * cervical dystonia
 * class of disease
 * focal dystonia
 * human disease
 * DOID:0050840
 * cervical endometrial stromal sarcoma
 * class of disease
 * cervix endometrial stromal tumor
 * Human disease
 * DOID:4520
 * cervical endometrioid adenocarcinoma
 * class of disease
 * cervical adenocarcinoma endometrial carcinoma
 * Human disease
 * DOID:5830
 * cervical incompetence
 * class of disease
 * abnormality of organs and soft tissues of pelvis complicating pregnancy, childbirth, or the puerperium cervix disease disease
 * cervix disease that is characterized by the beginning of dilation and effacement of a pregnant woman&#39;s cervix before her pregnancy has reached term
 * DOID:9681 DOID:9678
 * C12.050.351.500.852.593.120 C12.050.703.039.089.339 C12.100.250.852.593.120
 * cervical keratinizing squamous cell carcinoma
 * class of disease
 * cervical squamous cell carcinoma keratinizing squamous cell carcinoma
 * Human disease
 * DOID:7483
 * cervical large cell neuroendocrine carcinoma
 * class of disease
 * cervix carcinoma
 * Human disease
 * DOID:6659
 * cervical lymphoepithelioma-like carcinoma
 * class of disease
 * cervical squamous cell carcinoma
 * Human disease
 * DOID:7598
 * cervical mucinous adenocarcinoma
 * class of disease
 * cervical adenocarcinoma mucinous adenocarcinoma
 * Human disease
 * DOID:3701
 * cervical neuroblastoma
 * class of disease
 * extracranial neuroblastoma
 * extracranial neuroblastoma that has material basis in immature nerve cells
 * DOID:0050935
 * cervical non-keratinizing squamous cell carcinoma
 * class of disease
 * cervical squamous cell carcinoma
 * Human disease
 * DOID:7961
 * cervical polyp
 * class of disease
 * cervix disease Uterine polyp
 * cervix disease characterized by a benign polyp on the surface of the cervical canal
 * DOID:0060325
 * Cervical polyp
 * cervical serous adenocarcinoma
 * class of disease
 * cervical adenocarcinoma serous cystadenocarcinoma
 * Human disease
 * DOID:5752
 * cervical spinal canal and spinal cord meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:7915
 * cervical squamous cell carcinoma
 * class of disease
 * cervix carcinoma squamous cell carcinoma
 * cervix carcinoma that has material basis in squamous cells of the cervix
 * DOID:3744
 * cervical uterine cancer
 * class of disease
 * uterine cancer cervix disease uterine cervix neoplasm disease
 * cancer arising from the cervix
 * DOID:4362
 * Cervical cancer
 * Ca in situ, cervix 2.jpg
 * cervical verrucous carcinoma
 * class of disease
 * cervical squamous cell carcinoma papillary carcinoma of the cervix uteri verrucous carcinoma
 * Human disease
 * DOID:3743
 * cervicitis
 * class of disease
 * cervix disease disease
 * inflammation of the uterine cervix
 * DOID:2568
 * C13.351.500.852.593.150
 * Cervicitis
 * Herpetic Cervicitis (8539801948).jpg
 * cervicomedullary junction neoplasm
 * class of disease
 * infratentorial cancer Spinal cord cancer
 * Human disease
 * DOID:4707
 * cervix carcinoma
 * class of disease
 * cervical uterine cancer carcinoma
 * cervical cancer that is located in the cervix uteri or located in the cervical area and that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:2893
 * cervix disease
 * class of disease
 * uterine disease
 * human disease
 * DOID:2253
 * C13.351.500.852.593
 * Diseases and disorders of cervix uteri
 * cervix endometrial stromal tumor
 * class of disease
 * cervical uterine cancer
 * Human disease
 * DOID:4521
 * cervix endometriosis
 * class of disease
 * cervix disease endometriosis
 * Human disease
 * DOID:361
 * cervix erosion
 * class of disease
 * cervix disease disease
 * ectropion
 * DOID:3456
 * C13.351.500.852.593.112
 * Cervical ectropion
 * cervix melanoma
 * class of disease
 * cervical uterine cancer mucosal melanoma
 * Human disease
 * DOID:4413
 * cervix small cell carcinoma
 * class of disease
 * cervix carcinoma small cell carcinoma
 * Human disease
 * DOID:6740
 * cervix squamous papilloma
 * class of disease
 * cervical benign neoplasm papilloma
 * Human disease
 * DOID:9445
 * cervix uteri carcinoma in situ
 * class of disease
 * cervical intraepithelial neoplasia cervix disease uterus carcinoma in situ
 * Human disease
 * DOID:8991
 * cheilitis
 * class of disease
 * lip disease inflammation
 * inflammation of the lips
 * DOID:1762
 * C07.465.409.215
 * Cheilitis
 * chemical colitis
 * class of disease
 * colitis
 * colitis caused by introduction of various chemicals
 * DOID:0060186
 * cherry allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus avium plant fruit food product.
 * DOID:0060506
 * chest wall bone cancer
 * class of disease
 * bone cancer chest wall lymphoma
 * bone cancer and malignant neoplasm of chest wall that is located in the chest wall
 * DOID:6579
 * chest wall lymphoma
 * class of disease
 * malignant neoplasm of chest wall thoracic cancer lymphoma
 * thoracic cancer that is located in the chest wall
 * DOID:6758
 * chest wall parachordoma
 * class of disease
 * parachordoma chest wall lymphoma neoplasm of chest wall mesenchymal cell neoplasm
 * Human disease
 * DOID:8043
 * chiasmal syndrome
 * class of disease
 * optic nerve disease encephalopathy
 * optic nerve disease that is characterized by lesions of the optic chiasm, manifesting as various impairments of the sufferer&#39;s visual field according to the location of the lesion along the optic nerve
 * DOID:5655
 * chicken egg allergy
 * class of disease
 * egg allergy
 * egg allergy triggered by Gallus gallus eggs
 * DOID:0060492
 * chief cell adenoma
 * class of disease
 * parathyroid adenoma
 * Human disease
 * DOID:7607
 * childhood absence epilepsy
 * class of disease symptom or sign
 * absence seizure childhood electroclinical syndrome Idiopathic generalized epilepsy generalized seizure
 * childhood electroclinical syndrome characterized by the occurrence of typical absence seizures, starting between the age of four and ten years
 * DOID:1825
 * childhood acute lymphocytic leukemia
 * class of disease
 * acute lymphocytic leukemia childhood leukemia
 * acute lymphocytic leukemia occuring during childhood
 * DOID:0080144
 * childhood acute megakaryoblastic leukemia
 * class of disease
 * acute megakaryoblastic leukemia
 * disease
 * DOID:0080794
 * childhood acute myeloid leukemia
 * class of disease
 * childhood leukemia bilineal acute myeloid leukemia acute myeloid leukemia
 * Acute myeloid leukemia occurring in childhood
 * DOID:0070323
 * childhood asthma
 * class of disease
 * asthma chronic asthma
 * human disease
 * DOID:0080815
 * childhood botryoid rhabdomyosarcoma
 * class of disease
 * botryoid embryo rhabdomyosarcoma Childhood Rhabdomyosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:6786
 * childhood brain germinoma
 * class of disease
 * brain germinoma childhood central nervous system germinoma
 * Human disease
 * DOID:7429
 * childhood brain meningioma
 * class of disease
 * brain meningioma rare childhood malignant neoplasm pediatric meningioma
 * Human disease
 * DOID:6939
 * childhood brain stem glioma
 * class of disease
 * childhood brain stem neoplasm Brainstem glioma rare childhood malignant neoplasm
 * Human disease
 * DOID:6383
 * childhood brain stem neoplasm
 * class of disease
 * brain stem neoplasm childhood cancer childhood infratentorial neoplasm brain stem cancer
 * Human disease
 * DOID:4206
 * childhood brainstem astrocytoma
 * class of disease
 * childhood brain stem glioma brain stem astrocytic neoplasm
 * human disease
 * DOID:6386
 * childhood central nervous system germinoma
 * class of disease
 * central nervous system germinoma malignant childhood germ cell neoplasm
 * Human disease
 * DOID:8078
 * childhood central nervous system immature teratoma
 * class of disease
 * central nervous system immature teratoma
 * Human disease
 * DOID:6654
 * childhood central nervous system mature teratoma
 * class of disease
 * central nervous system mature teratoma pediatric central nervous system tumor
 * Human disease
 * DOID:6423
 * childhood central nervous system mixed germ cell tumor
 * class of disease
 * central nervous system childhood germ cell tumor malignant childhood germ cell neoplasm mixed germ cell tumor of central nervous system rare childhood malignant neoplasm brain cancer
 * Human disease
 * DOID:7516
 * childhood central nervous system primitive neuroectodermal neoplasm
 * class of disease
 * central nervous system primitive neuroectodermal neoplasm childhood cancer
 * Human disease
 * DOID:3870
 * childhood cerebellar astrocytic neoplasm
 * class of disease
 * cerebellar astrocytoma childhood cerebellar neoplasm juvenile astrocytoma
 * Human disease
 * DOID:6286
 * childhood cerebellar neoplasm
 * class of disease
 * cerebellum cancer childhood infratentorial neoplasm
 * Human disease
 * DOID:5059
 * childhood cerebral astrocytoma
 * class of disease
 * cerebrum cancer juvenile astrocytoma
 * Human disease
 * DOID:7007
 * childhood choriocarcinoma of the ovary
 * class of disease
 * choriocarcinoma of ovary rare childhood malignant neoplasm non-gestational ovarian choriocarcinoma malignant childhood germ cell neoplasm pediatric ovarian germ cell tumor
 * Human disease
 * DOID:8336
 * childhood choriocarcinoma of the testis
 * class of disease
 * choriocarcinoma of the testis rare childhood malignant neoplasm malignant childhood germ cell neoplasm pediatric testicular germ cell tumor
 * Human disease
 * DOID:6160
 * childhood choroid plexus cancer
 * class of disease
 * childhood cancer childhood choroid plexus neoplasm choroid plexus neoplasm
 * Human disease
 * DOID:3545
 * childhood disintegrative disease
 * class of disease
 * pervasive developmental disorder disease
 * neurodevelopmental condition
 * DOID:13487
 * childhood electroclinical syndrome
 * class of disease
 * electroclinical syndrome Epilepsy in children absence seizure
 * electroclinical syndrome with onset in childhood between one and 12 years of age
 * DOID:0050704
 * childhood embryonal testis carcinoma
 * class of disease
 * embryonal testis carcinoma rare childhood malignant neoplasm malignant childhood germ cell neoplasm pediatric testicular germ cell tumor
 * embryonal testis carcinoma that occurs in children
 * DOID:6162
 * childhood endodermal sinus tumor
 * class of disease
 * endodermal sinus tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm
 * endodermal sinus tumor that occurs in children
 * DOID:5342
 * childhood extraosseous osteosarcoma
 * class of disease
 * extraosseous osteosarcoma pediatric osteosarcoma
 * Human disease
 * DOID:7297
 * childhood germ cell brain tumor
 * class of disease
 * central nervous system childhood germ cell tumor brain cancer
 * Human disease
 * DOID:7430
 * childhood hypophosphatasia
 * class of disease
 * hypophosphatasia
 * A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.
 * DOID:0110915
 * childhood immature teratoma of ovary
 * class of disease
 * immature teratoma of ovary rare childhood malignant neoplasm malignant childhood germ cell neoplasm childhood teratoma of the ovary
 * Human disease
 * DOID:7037
 * childhood infratentorial neoplasm
 * class of disease
 * brain stem cancer infratentorial cancer childhood neoplasm childhood brain tumor
 * Human disease
 * DOID:4207
 * childhood intracortical osteosarcoma
 * class of disease
 * pediatric osteosarcoma intracortical osteogenic sarcoma
 * human disease
 * DOID:7612
 * childhood kidney angiomyolipoma
 * class of disease
 * childhood kidney neoplasm kidney angiomyolipoma
 * Human disease
 * DOID:8410
 * childhood kidney cell carcinoma
 * class of disease
 * renal cell carcinoma rare childhood malignant neoplasm childhood malignant kidney neoplasm
 * Human disease
 * DOID:4454
 * childhood kidney neoplasm
 * class of disease
 * kidney neoplasm childhood neoplasm kidney cancer
 * Human disease
 * DOID:3675
 * childhood leukemia
 * class of disease
 * leukemia childhood cancer rare childhood malignant neoplasm bone marrow cancer
 * leukemia that occurs in children
 * DOID:7757
 * childhood malignant hemangiopericytoma
 * class of disease
 * hemangiopericytoma hemangiopericytoma, malignant
 * Human disease
 * DOID:7731
 * childhood malignant mesenchymoma
 * class of disease
 * malignant mesenchymoma childhood cancer
 * Human disease
 * DOID:5893
 * childhood malignant schwannoma
 * class of disease
 * malignant peripheral nerve sheath tumor neurilemmoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7732
 * childhood mature teratoma of the ovary
 * class of disease
 * childhood teratoma of the ovary mature teratoma of the ovary
 * Human disease
 * DOID:6229
 * childhood mediastinal neurogenic tumor
 * class of disease
 * malignant mediastinal neurogenic neoplasm childhood neoplasm
 * Human disease
 * DOID:4690
 * childhood medulloblastoma
 * class of disease
 * medulloblastoma childhood infratentorial neoplasm
 * Human disease
 * DOID:3869
 * childhood multilocular cystic kidney neoplasm
 * class of disease
 * kidney benign neoplasm childhood kidney neoplasm multiloculated renal cyst
 * A childhood renal Wilms cancer that occurs in children. It encompasses two histologically distinct but grossly indistinguishable lesions: cystic nephroma and cystic partially differentiated nephroblastoma (CPDN).
 * DOID:7762
 * childhood oligodendroglioma
 * class of disease
 * oligodendroglioma
 * Human disease
 * DOID:3183
 * childhood onset epileptic encephalopathy
 * class of disease
 * generalized epilepsy Epilepsy in children
 * An idiopathic generalized epilepsy characterized by onset of multiple seizure types in the first few years of life and associated with poor prognosis. Affected individuals have cognitive regression and intellectual disability.
 * DOID:0060475
 * childhood optic nerve glioma
 * class of disease
 * optic nerve glioma
 * human disease
 * DOID:6576
 * childhood ovarian embryonal carcinoma
 * class of disease
 * ovarian embryonal carcinoma pediatric ovarian germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm
 * ovarian embryonal carcinoma that occurs in childhood
 * DOID:8036
 * childhood ovarian endodermal sinus tumor
 * class of disease
 * ovarian endodermal sinus tumor pediatric ovarian germ cell tumor childhood endodermal sinus tumor
 * Human disease
 * DOID:6083
 * childhood parosteal osteogenic sarcoma
 * class of disease
 * juxtacortical osteosarcoma pediatric osteosarcoma
 * Human disease
 * DOID:5809
 * childhood pilocytic astrocytoma
 * class of disease
 * pilocytic astrocytoma
 * Human disease
 * DOID:6812
 * childhood pleomorphic rhabdomyosarcoma
 * class of disease
 * pleomorphic rhabdomyosarcoma Childhood Rhabdomyosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7463
 * childhood spinal cord tumor
 * class of disease
 * Spinal cord cancer childhood cancer
 * Human disease
 * DOID:3637
 * childhood teratocarcinoma of the testis
 * class of disease
 * childhood testicular mixed germ cell tumor
 * Human disease
 * DOID:6474
 * childhood teratoma of the ovary
 * class of disease
 * ovarian germ cell teratoma pediatric ovarian germ cell tumor
 * Human disease
 * DOID:6230
 * childhood testicular mixed germ cell tumor
 * class of disease
 * mixed testicular germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm pediatric testicular germ cell tumor
 * Human disease
 * DOID:6161
 * childhood type dermatomyositis
 * class of disease
 * dermatomyositis
 * Human disease
 * DOID:14203
 * childhood vagina botryoid rhabdomyosarcoma
 * class of disease
 * vagina botryoid rhabdomyosarcoma childhood botryoid rhabdomyosarcoma
 * Human disease
 * DOID:6787
 * chloramine T respiratory allergy
 * class of disease
 * metal allergy respiratory allergy
 * respiratory allergy that has allergic trigger chloramine T
 * DOID:0040062
 * chlorhexidine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger chlorhexidine
 * DOID:0040026
 * cholangiocarcinoma
 * class of disease
 * bile duct adenocarcinoma disease
 * bile duct adenocarcinoma that has material basis in bile duct epithelial cells.
 * DOID:4947
 * C04.557.470.200.025.450
 * Cholangiocarcinoma
 * ERCP cholangioca.jpg
 * cholangiolocellular carcinoma
 * class of disease
 * intrahepatic cholangiocarcinoma rare parenchymal liver disease
 * Human disease
 * DOID:7642
 * cholecystitis
 * class of disease symptom or sign
 * ascending cholangitis disease
 * cholangitis that is characterized by an inflammation that is located in the gallbladder
 * DOID:1949
 * C06.130.564.263
 * Cholecystitis
 * cholecystolithiasis
 * class of disease
 * gallbladder disease gallstone
 * Human disease
 * DOID:11151
 * C06.130.409.178 C06.130.564.332
 * choledochal cyst
 * class of disease
 * bile duct disease disease
 * congenital disorder of digestive system
 * DOID:899
 * C04.182.198 C06.130.120.127 C06.198.184 C16.131.314.184
 * Choledochal cysts
 * choledocholithiasis
 * class of disease
 * gallbladder disease common bile duct disease endocrine system disease disease
 * Human disease
 * DOID:11755
 * C06.130.120.250.174 C06.130.409.267
 * Choledocholithiasis
 * MRCP Choledocholithiasis.jpg
 * cholelithiasis
 * class of disease
 * gallbladder disease disease
 * Human disease
 * DOID:10211
 * C06.130.409
 * Cholelithiasis
 * Gallstones.jpg
 * cholestasis
 * class of disease
 * bile duct disease disease
 * Human disease
 * DOID:13580
 * C06.130.120.135
 * Cholestasis
 * Bilirubin pigment in cholestatic liver 40X.jpg
 * cholesteatoma
 * class of disease
 * keratosis disease
 * keratosis characterized by keratinizing squamous epithelium located in middle ear and/or mastoid, subepithelial connective tissue and by the progressive accumulation of keratin debris with or without surrounding inflammatory reaction
 * DOID:869
 * C17.800.428.260
 * Cholesteatoma
 * Cholesteatom kuppelraum 1a.jpg
 * cholesterol embolism
 * class of disease
 * vascular disease embolism
 * vascular disease with blood vessel obstruction resulting from the release of cholesterol
 * DOID:1461
 * C14.907.355.350.454.500
 * Cholesterol embolism
 * choline deficiency disease
 * class of disease
 * nutritional deficiency disease
 * Human disease
 * DOID:8456
 * C18.654.521.500.133.699.160
 * cholinergic urticaria
 * class of disease
 * physical urticaria disease
 * urticaria induced by sweating
 * DOID:14443
 * chondroblastic osteosarcoma
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3372
 * chondroblastoma
 * class of disease
 * connective tissue neoplasm connective tissue benign neoplasm benign neoplasms by histologic type disease
 * Human disease
 * DOID:2649
 * C04.557.450.565.250
 * Chondroblastoma
 * Chondroblastoma - very high mag.jpg
 * chondrodysplasia with joint dislocations gPAPP type
 * class of disease
 * autosomal recessive disease osteochondrodysplasia
 * human disease
 * DOID:0112224
 * chondroid chordoma
 * class of disease
 * chordoma
 * chordoma that histologically derives from chordoma, derives from chondroma, and derives from chondrosarcoma
 * DOID:4152
 * chondroid lipoma
 * class of disease
 * lipoma
 * lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women
 * DOID:10208
 * chondroid syringoma of the vulva
 * class of disease
 * eccrine mixed tumor of skin vulvar benign neoplasm
 * Human disease
 * DOID:2078
 * chondroma
 * class of disease
 * benign neoplasms by histologic type cartilage tumor disease
 * cell type benign neoplasm that is a cartilaginous tumor encapsulated with a lobular growing pattern
 * DOID:2602
 * C04.557.450.565.265
 * Chondroma
 * chondromalacia
 * class of disease
 * articular cartilage disease
 * DOID:2557
 * chondropathy
 * class of disease
 * osteochondropathy connective tissue disease disease
 * human disease
 * DOID:1222
 * C05.182 C17.300.182
 * Chondropathies
 * chordoid meningioma
 * class of disease
 * clear cell meningioma
 * Human disease
 * DOID:8368
 * chordoma
 * class of disease
 * notochordal cancer disease
 * notochordal cancer that derives from cellular remnants of the notochord
 * DOID:3302
 * C04.557.465.220
 * Chordoma
 * Chordoma.JPG
 * chorea gravidarum
 * class of disease
 * choreatic disease complications of pregnancy disease
 * Human disease
 * DOID:14483
 * C10.228.140.079.294 C10.228.662.262.249.500 C13.703.141
 * chorioamnionitis
 * class of disease
 * placenta disease disease
 * placenta disease that is an inflammation of the fetal membranes (amnion and chorion) due to a bacterial infection
 * DOID:0050697
 * C13.703.277.030 C13.703.420.339.260 C13.703.590.268 C16.300.030
 * Chorioamnionitis
 * Chorioamnionitis - high mag.jpg
 * chorioangioma
 * class of disease
 * placenta disease uterine benign neoplasm hemangioma
 * Human disease
 * DOID:277
 * Chorangioma
 * Chorangioma - low mag.jpg
 * choriocarcinoma
 * class of disease
 * placenta cancer trophoblastic neoplasm disease
 * Human disease
 * DOID:3594
 * C04.557.465.955.207 C04.557.470.200.025.455 C04.850.908.208 C13.703.720.949.208
 * Choriocarcinoma
 * Metastatic choriocarcinoma Case 140 (4858357750).jpg
 * choriocarcinoma of ovary
 * class of disease
 * malignant ovarian germ cell neoplasm non-gestational choriocarcinoma choriocarcinoma
 * Human disease
 * DOID:5550
 * choriocarcinoma of the testis
 * class of disease
 * non-gestational choriocarcinoma testicular non-seminomatous germ cell cancer choriocarcinoma
 * Human disease
 * DOID:5551
 * chorioretinal scar
 * class of disease
 * retinal disease scar
 * Human disease
 * DOID:11086
 * chorioretinitis
 * class of disease symptom or sign
 * eye disease uveitis disease
 * inflammation of the choroid
 * DOID:8886
 * C11.768.773.348 C11.941.160.478.400 C11.941.879.780.900.300.318
 * Chorioretinitis
 * Chorioretinitis AIDS nci-vol-2169-300.jpg
 * choroid cancer
 * class of disease
 * uveal cancer choroid neoplasm choroid disease
 * Human disease
 * DOID:12759
 * choroid disease
 * class of disease
 * uveal disease
 * human disease
 * DOID:1417
 * C11.941.160
 * choroid plexus carcinoma
 * class of disease
 * choroid plexus neoplasm carcinoma
 * choroid plexus cancer that has material basis in epithelial cells of the choroid plexus
 * DOID:5648
 * Choroid plexus carcinoma
 * Choroidplexuscarcinoma.png
 * choroid plexus meningioma
 * class of disease
 * choroid plexus neoplasm meningioma cerebral meningioma
 * Human disease
 * DOID:4584
 * choroid plexus neoplasm
 * class of disease
 * cerebral ventricle neoplasm cerebral ventricle cancer
 * cerebral ventricle neoplasm that is located in the plexus located in the ventricles of the brain
 * DOID:3540
 * C04.588.614.250.195.205.200 C10.228.140.211.280.300 C10.551.240.250.200.200
 * Choroid plexus cancers
 * choroid plexus papilloma
 * class of disease
 * papilloma choroid plexus neoplasm cerebrovascular benign neoplasm
 * Benign brain tumor
 * DOID:2626
 * C04.588.614.250.195.205.200.500 C10.228.140.211.280.300.500 C10.551.240.250.200.200.500
 * Choroid plexus papilloma
 * Plexuspapillom Makroskopie.png
 * choroidal sclerosis
 * class of disease
 * eye degenerative disease choroid disease
 * neurodegenerative disease that involves the optic choroid
 * DOID:980
 * choroiditis
 * class of disease
 * choroid disease uveitis
 * inflammation of the choroid
 * DOID:11406
 * C11.941.160.478 C11.941.879.780.900.300
 * chromium allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis metal allergy
 * allergic contact dermatitis that has allergic trigger chromium atom
 * DOID:0040056
 * chromophobe renal cell carcinoma
 * class of disease
 * renal cell carcinoma
 * renal cell carcinoma that has material basis in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells
 * DOID:4471
 * Chromophobe renal cell carcinoma
 * chromosomal deletion syndrome
 * class of disease
 * chromosomal disease
 * Human disease
 * DOID:0060388
 * C23.550.210.050.500.500 G05.365.590.029.530.175 G05.365.590.175.050.500.500 G05.365.590.762.180 G05.558.800.180 G05.700.131.500.500
 * Chromosome deletion
 * chromosomal duplication syndrome
 * class of disease
 * chromosomal disease
 * Human disease
 * DOID:0060429
 * C23.550.210.182
 * chromosome 10q23 deletion syndrome
 * class of disease
 * chromosomal deletion syndrome partial monosomy of the long arm of chromosome 10
 * Human disease
 * DOID:0060389
 * chromosome 13q14 deletion syndrome
 * class of disease
 * chromosomal deletion syndrome autosomal dominant disease
 * Human disease
 * DOID:0060391
 * chromosome 17p13.1 deletion syndrome
 * class of disease
 * chromosomal deletion syndrome classical lissencephalies and subcortical band heterotopias autosomal dominant disease partial monosomy of the short arm of chromosome 17
 * Human disease
 * DOID:0060402
 * chromosome 18p deletion syndrome
 * class of disease
 * chromosomal deletion syndrome autosomal dominant disease
 * human disease
 * DOID:0060406
 * chromosome 18q deletion syndrome
 * class of disease
 * chromosomal deletion syndrome partial deletion of the long arm of chromosome 18 autosomal dominant disease
 * human disease
 * DOID:0060407
 * Distal 18q-
 * chromosome 19p13.13 deletion syndrome
 * class of disease
 * chromosomal deletion syndrome autosomal dominant disease partial deletion of the short arm of chromosome 19
 * Human disease
 * DOID:0060426
 * chromosome 1q41-q42 deletion syndrome
 * class of disease
 * chromosomal deletion syndrome
 * Human disease
 * DOID:0060412
 * chromosome 3-linked frontotemporal dementia
 * class of disease
 * frontotemporal dementia
 * A frontotemporal dementia that has material basis in heterozygous mutation in CHMP2B on 3p11.2.
 * DOID:0111227
 * chromosome Xp11.22 duplication syndrome
 * class of disease
 * partial duplication of the short arm of chromosome X non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112037
 * chronic NK-cell lymphocytosis
 * class of disease
 * type IV hypersensitivity mature T-cell neoplasm
 * Human disease
 * DOID:7465
 * chronic apical periodontitis
 * class of disease
 * periapical periodontitis
 * Human disease
 * DOID:11269
 * chronic asthma
 * class of disease
 * asthma
 * human disease
 * DOID:0080809
 * chronic atticoantral disease
 * class of disease
 * chronic purulent otitis media
 * Human disease
 * DOID:14248
 * chronic cervicitis
 * class of disease
 * cervicitis
 * Human disease
 * DOID:1513
 * chronic cholangitis
 * class of disease
 * ascending cholangitis
 * Human disease
 * DOID:9439
 * chronic closed-angle glaucoma
 * class of disease
 * primary angle-closure glaucoma
 * Human disease
 * DOID:14445
 * chronic conjunctivitis
 * class of disease
 * conjunctivitis
 * Human disease
 * DOID:2475
 * chronic cystitis
 * class of disease
 * cystitis chronic condition
 * Recurrent infections of the urinary bladder
 * DOID:1680
 * Chronic cystitis
 * chronic dacryoadenitis
 * class of disease
 * dacryoadenitis
 * Human disease
 * DOID:949
 * chronic dacryocystitis
 * class of disease
 * chronic inflammation of lacrimal passage dacryocystitis
 * Human disease
 * DOID:9937
 * chronic duodenal ileus
 * class of disease
 * duodenal obstruction
 * Human disease
 * DOID:13687
 * chronic eosinophilic leukemia
 * class of disease
 * chronic leukemia eosinophilic leukemia
 * human disease
 * DOID:0080367
 * chronic ethmoiditis
 * class of disease
 * ethmoid sinusitis chronic rhinosinusitis
 * ethmoid sinusitis which lasts for 12 weeks or more
 * DOID:9312
 * chronic eustachian salpingitis
 * class of disease
 * otosalpingitis
 * otosalpingitis which is persistent and long-lasting
 * DOID:1999
 * chronic fatigue syndrome
 * class of disease symptom or sign
 * syndrome primary immunodeficiency disease disease
 * medical condition involving extreme fatigue and a wide range of other symptoms
 * DOID:8544
 * C02.330 C05.651.310 C10.228.440.600 C10.668.364
 * [[File:Statistical parametric maps of BPND of 11C-(R)-PK11195 in CFS.ME patients and healthy controls.gif|center|64px]]
 * chronic follicular conjunctivitis
 * class of disease
 * chronic conjunctivitis
 * Human disease
 * DOID:13326
 * chronic frontal sinusitis
 * class of disease
 * frontal sinusitis chronic condition
 * frontal sinusitis which lasts for 12 weeks or more. This causes steady headache, localized tenderness and intermittent, purulent nasal and postnasal drainage.
 * DOID:10790
 * chronic fungal otitis externa
 * class of disease
 * otomycosis fungal infectious disease
 * otomycosis which is persistent and long-lasting or recurrent
 * DOID:10519
 * chronic gastritis
 * class of disease
 * gastritis stomach disease
 * Inflammation of the stomach that is chronic in nature
 * DOID:4029
 * chronic gonococcal salpingitis
 * class of disease
 * chronic salpingitis gonococcal infectious diseases
 * Human disease
 * DOID:12718
 * chronic gonorrhea of cervix
 * class of disease
 * chronic cervicitis gonococcal infectious diseases
 * Human disease
 * DOID:1512
 * chronic inducible urticaria
 * class of disease
 * chronic urticaria
 * human disease
 * DOID:0080748
 * C17.800.862.945.533.500 C20.543.480.904.533.500 C23.550.291.500.360.500
 * chronic inflammation of lacrimal passage
 * class of disease
 * chronic inflammatory response lacrimal apparatus disease
 * Human disease
 * DOID:9935
 * chronic inflammatory demyelinating polyneuritis
 * class of disease
 * inflammatory and toxic neuropathy chronic inflammatory demyelinating polyradiculoneuropathy demyelinating polyneuropathy
 * An immunologic inflammatory disorder characterized by loss of myelin in the peripheral nerves. Patients present with progressive weakness and loss of sensory function in the legs and arms.
 * DOID:2536
 * chronic interstitial cystitis
 * class of disease
 * interstitial cystitis chronic cystitis
 * human disease
 * DOID:1678
 * chronic intestinal vascular insufficiency
 * class of disease
 * intestinal disease
 * Human disease
 * DOID:8633
 * chronic lacrimal gland enlargement
 * class of disease
 * dacryoadenitis
 * Human disease
 * DOID:12809
 * chronic laryngitis
 * class of disease
 * laryngitis
 * A laryngitis in which symptoms last longer than three weeks. Gastroesophageal reflux, and lingering bronchitis can cause the disease.
 * DOID:11797
 * chronic leukemia
 * class of disease
 * leukemia
 * broad type of leukemia; disjoint with acute leukemia
 * DOID:1036
 * Chronic leukemias
 * chronic lymphocytic leukemia
 * class of disease symptom or sign
 * lymphoblastic leukemia chronic leukemia small lymphocytic lymphoma lymphoma leukemia disease
 * lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood
 * DOID:1040
 * C04.557.337.428.080.125 C15.604.515.560.080.125 C20.683.515.528.080.125 C15.378.508.428.080.125 C23.550.291.500.483
 * Chronic lymphocytic leukemia
 * Chronic lymphocytic leukemia.jpg
 * chronic lymphocytic leukemia and small lymphocytic lymphoma
 * class of disease
 * chronic lymphocytic leukemia
 * chronic lymphocytic leukemia that is characterized by the presence of immature lymphocytes in the blood and bone marrow and/or in the lymph nodes
 * DOID:6354
 * chronic maxillary sinusitis
 * class of disease
 * maxillary sinusitis chronic condition
 * maxillary sinusitis which lasts for 12 weeks or more
 * DOID:10792
 * chronic meningitis
 * class of disease
 * meningitis
 * Human disease
 * DOID:10341
 * chronic metabolic polyneuropathy
 * class of disease
 * chronic polyneuropathy
 * Human disease
 * DOID:7441
 * chronic monocytic leukemia
 * class of disease
 * monocytic leukemia chronic myelomonocytic leukemia
 * human disease
 * DOID:8593
 * chronic myeloid leukemia
 * class of disease
 * myeloid leukemia chronic leukemia disease
 * myeloid leukemia that is characterized by over production of white blood cells
 * DOID:8552
 * C04.557.337.539.250 C15.378.190.636.370
 * Chronic myeloid leukemia
 * Bcrablmet.jpg
 * chronic myelomonocytic leukemia
 * class of disease
 * monocytic leukemia chronic myeloid leukemia chronic leukemia
 * chronic leukemia characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood
 * DOID:0080188
 * C04.557.337.539.522 C15.378.190.615.510 C15.378.508.539.522 C23.550.291.500.495
 * Chronic myelomonocytic leukemia
 * chronic neutrophilic leukemia
 * class of disease
 * myeloproliferative disorders chronic leukemia
 * chronic leukemia characterized by neutrophilic leukocytosis with no detectable Philadelphia chromosome or BCR/ABL fusion gene
 * DOID:0080187
 * C15.378.190.636.380
 * chronic obstructive pulmonary disease
 * class of disease
 * obstructive lung disease disease
 * lung disease involving long-term poor airflow
 * DOID:3083
 * C08.381.495.389 C23.550.291.500.875
 * Chronic obstructive pulmonary disease
 * Centrilobular emphysema 865 lores.jpg
 * chronic orbital inflammation
 * class of disease
 * orbital disease chronic inflammatory response
 * Human disease
 * DOID:1397
 * chronic perichondritis of pinna
 * class of disease
 * perichondritis of auricle pinna disease
 * perichondritis of auricle which is persistent and long-lasting
 * DOID:14243
 * chronic polyneuropathy
 * class of disease
 * polyneuropathy
 * Human disease
 * DOID:5221
 * chronic pulmonary eosinophilia
 * class of disease
 * eosinophilic pneumonia
 * An eosinophilic pneumonia which slowly progresses over weeks to months. Life-threatening shortness of breath can develop if the condition is not treated. Individuals are often diagnosed with asthma before the advent of this disease.
 * DOID:9502
 * chronic pulmonary heart disease
 * class of disease
 * cor pulmonale
 * Human disease
 * DOID:12326
 * chronic purulent otitis media
 * class of disease
 * suppurative otitis media chronic otitis media
 * suppurative otitis media which is persistent and long-lasting
 * DOID:14247
 * chronic pyelonephritis
 * class of disease
 * pyelonephritis
 * Human disease
 * DOID:1076
 * Chronic pyelonephritis
 * chronic rapidly progressive glomerulonephritis
 * class of disease
 * glomerulonephritis rapidly progressive glomerulonephritis
 * Human disease
 * DOID:11036
 * chronic rheumatic pericarditis
 * class of disease
 * pericarditis rheumatic heart disease
 * human disease
 * DOID:1869 DOID:14044
 * chronic salpingitis
 * class of disease
 * salpingitis
 * Human disease
 * DOID:5731
 * chronic salpingo-oophoritis
 * class of disease
 * salpingo-oophoritis
 * Human disease
 * DOID:12265
 * chronic sphenoidal sinusitis
 * class of disease
 * sphenoid sinusitis chronic condition
 * sphenoid sinusitis which lasts for 12 weeks or more
 * DOID:10793
 * chronic spontaneous urticaria
 * class of disease
 * chronic urticaria idiopathic urticaria
 * human disease
 * DOID:0080749
 * Chronic spontaneous urticaria
 * Chronic spontaneous urticaria.jpg
 * chronic subinvolution of uterus
 * class of disease
 * uterine disease
 * Human disease
 * DOID:13811
 * chronic toxic polyneuropathy
 * class of disease
 * chronic polyneuropathy
 * Human disease
 * DOID:7825
 * chronic tubotympanic suppurative otitis media
 * class of disease
 * chronic purulent otitis media suppurative otitis media
 * Human disease
 * DOID:14435
 * chronic tympanitis
 * class of disease
 * tympanic membrane disease myringitis
 * Human disease
 * DOID:11217
 * chronic ulcer of skin
 * class of disease symptom or sign
 * skin disease ulcer
 * human disease
 * DOID:8549
 * chronic urticaria
 * class of disease
 * urticaria
 * urticaria with symptoms lasting for more than 6 weeks
 * DOID:0080747
 * C17.800.862.945.533 C20.543.480.904.533
 * chronic venous insufficiency
 * class of disease
 * venous insufficiency disease
 * Human disease
 * DOID:0050853
 * Chronic venous insufficiency
 * chronic wasting disease
 * class of disease
 * animal disease transmissible spongiform encephalopathy
 * animal disease
 * DOID:3530
 * C10.228.228.800.858 C10.574.843.925 C22.955 C01.207.800.858
 * Chronic wasting disease
 * Deer1 tkreeger.jpg
 * chylocele of tunica vaginalis
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:10835
 * cicatricial ectropion
 * class of disease
 * ectropion
 * Human disease
 * DOID:12782
 * cicatricial entropion
 * class of disease
 * entropion
 * Human disease
 * DOID:13113
 * cicatricial lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:13038
 * cicatricial pemphigoid
 * class of disease
 * bullous skin disease pemphigoid eye inflammation autoimmune disease of musculoskeletal system
 * autoimmune blistering disease
 * DOID:11656
 * C11.187.482 C17.800.865.670
 * ciliary body cancer
 * class of disease
 * iris cancer ciliary body neoplasm ciliary body disease
 * Human disease
 * DOID:4352
 * ciliary body disease
 * class of disease
 * iris disease
 * Human disease
 * DOID:4353
 * citrullinemia type I
 * class of disease
 * citrullinemia
 * medical condition
 * DOID:0070340
 * classic congenital mesoblastic nephroma
 * class of disease
 * congenital mesoblastic nephroma
 * Human disease
 * DOID:8083
 * classic pulmonary blastoma
 * class of disease
 * pulmonary blastoma
 * Human disease
 * DOID:4767
 * classic type lipoma
 * class of disease
 * lipoma
 * Human disease
 * DOID:10193
 * classic variant of chromophobe renal cell carcinoma
 * class of disease
 * chromophobe renal cell carcinoma
 * Human disease
 * DOID:6605
 * clear cell acanthoma
 * class of disease
 * skin benign neoplasm acanthoma
 * Human disease
 * DOID:172
 * clear cell adenocarcinoma
 * class of disease
 * adenocarcinoma clear cell carcinoma
 * adenocarcinoma that derives from epithelial cells which have clear cytoplasm
 * DOID:4468
 * C04.557.470.200.025.045
 * clear cell adenofibroma
 * class of disease
 * adenofibroma
 * benign neoplasm characterized by the presence of glandular structures which contain clear cells and a fibrotic stroma
 * DOID:5477
 * clear cell adenoma
 * class of disease
 * adenoma
 * adenoma that is composed of cells with a clear cytoplasm located in ovary
 * DOID:5390
 * clear cell basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4293
 * clear cell carcinoma
 * class of disease
 * carcinoma connective tissue benign neoplasm clear-cell tumor sarcoma
 * carcinoma (i.e. not a sarcoma) showing clear cells
 * DOID:4233
 * clear cell chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5867
 * C04.557.450.565.280.140 C04.557.450.795.300.140
 * clear cell cystadenofibroma
 * class of disease
 * cystadenofibroma clear cell adenofibroma
 * benign neoplasm characterized by the presence of cystic glandular and fibrous tissues and clear cells
 * DOID:5895
 * clear cell ependymoma
 * class of disease
 * benign ependymoma
 * ependymoma, often supratentorial in location, characterized by the presence of ependymal cells with a perinuclear halo
 * DOID:5507
 * clear cell hidradenoma
 * class of disease
 * hidradenoma clear cell adenoma
 * Human disease
 * DOID:5443
 * clear cell meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:4210
 * clear cell squamous cell skin carcinoma
 * class of disease
 * cutaneous squamous-cell carcinoma clear cell carcinoma keratinizing squamous cell carcinoma
 * Human disease
 * DOID:8288
 * clear cell variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:6476
 * clear-cell ovarian carcinoma
 * class of disease
 * ovarian carcinoma clear cell carcinoma ovarian clear cell tumor
 * ovarian carcinoma that has material basis in cells with clear cytoplasm and glycogen secreting hob nail cells
 * DOID:0050934 DOID:5305
 * Clear-cell ovarian carcinoma
 * cleft lip
 * class of disease
 * lip disease cleft lip and cleft palate
 * human disease
 * DOID:9296
 * C07.465.409.225 C07.465.525.164 C07.650.525.164 C16.131.850.525.164
 * cleft palate
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate
 * DOID:674
 * C05.500.460.185 C05.660.207.540.460.185 C07.320.440.185 C07.465.525.185 C07.650.500.460.185 C07.650.525.185 C16.131.621.207.540.460.185 C16.131.850.500.460.185 C16.131.850.525.185
 * Cleft palate
 * cleft soft palate
 * class of disease
 * cleft palate
 * Cleft velum is a fissure type embryopathy that affects in varying degrees the soft palate
 * DOID:0110214
 * clitoris cancer
 * class of disease
 * clitoris neoplasm
 * human disease
 * DOID:2401
 * cloacogenic carcinoma
 * class of disease
 * anal squamous cell carcinoma anal canal carcinoma
 * Human disease
 * DOID:7173
 * co-trimoxazole allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger co-trimoxazole
 * DOID:0040070
 * cobalt allergic asthma
 * class of disease
 * allergic asthma cobalt allergy metal allergy
 * allergic asthma that has allergic trigger cobalt atom
 * DOID:0040054
 * cobalt allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis cobalt allergy metal allergy
 * allergic contact dermatitis that has allergic trigger cobalt atom
 * DOID:0040053
 * cobblestone retinal degeneration
 * class of disease
 * peripheral retinal degeneration
 * Human disease
 * DOID:12166
 * cocaine dependence
 * class of disease
 * cocaine-related disorder substance dependence substance abuse disease
 * drug dependence that is a psychological dependency on the regular use of cocaine
 * DOID:9975 DOID:809
 * coccidioidomycosis
 * class of disease
 * primary systemic mycosis disease
 * fungal infection
 * DOID:13450
 * C01.150.703.203
 * Coccidioidomycosis
 * Coccidioidomycosis granulomas on forehead.png
 * coenurosis
 * class of disease
 * parasitic helminthiasis infectious disease Coenurosis skin disease central nervous system disease
 * Human disease
 * DOID:0050251
 * cognitive disorder
 * class of disease
 * mental disorder organic brain syndrome
 * disease of mental health that affects cognitive functions including memory processing, perception and problem solving
 * DOID:1561
 * F03.615.250
 * Neurocognitive disorders
 * cold-induced sweating syndrome 1
 * class of disease
 * cold-induced sweating syndrome
 * human disease
 * DOID:0080329
 * cold-induced sweating syndrome 2
 * class of disease
 * cold-induced sweating syndrome
 * cold-induced sweating syndrome that has material basis in compound heterozygous mutation in the CLCF1 gene on chromosome 11q13
 * DOID:0080330
 * cold-induced sweating syndrome 3; CISS3
 * class of disease
 * cold-induced sweating syndrome
 * human disease
 * DOID:0080331
 * colitis
 * class of disease
 * inflammatory bowel diseases colonic disease disease
 * inflammation of the colon or the large intestine
 * DOID:0060180
 * C06.405.205.265 C06.405.469.158.188
 * Colitis
 * Cryptitis high mag.jpg
 * collagen disease
 * class of disease
 * connective tissue disease
 * group of diseases affecting connective tissue
 * DOID:854
 * C17.300.200
 * Collagen diseases
 * collagenous colitis
 * class of disease
 * microscopic colitis disease
 * colitis characterized by a distinctive thickening of the subepithelial collagen table
 * DOID:0060183
 * C06.405.205.265.173.500 C06.405.469.158.188.173.500
 * Collagenous colitis
 * colloid adenoma
 * class of disease
 * follicular adenoma
 * Human disease
 * DOID:8419
 * colloid carcinoma of the pancreas
 * class of disease
 * pancreatic carcinoma
 * Human disease
 * DOID:7717
 * coloboma of optic nerve
 * class of disease
 * coloboma optic nerve disease visual pathway disease
 * rare defect of the optic nerve that causes moderate to severe visual field defects.
 * DOID:11975
 * colon adenocarcinoma
 * class of disease
 * colon carcinoma adenocarcinoma
 * colon carcinoma that derives from epithelial cells of glandular origin
 * DOID:234
 * Metastatic colonic adenocarcinoma Case 165 (5477628150).jpg
 * colon adenoma
 * class of disease
 * colonic benign neoplasm benign neoplasms by histologic type colorectal adenoma adenoma
 * colonic benign neoplasm that has material basis in epithelial tissue with glandular origin
 * DOID:0050912
 * colon carcinoma
 * class of disease
 * plump cancer carcinoma
 * colon cancer that has material basis in abnormally proliferating cells derives_from epithelial cells
 * DOID:1520
 * colon leiomyoma
 * class of disease
 * leiomyoma colonic benign neoplasm colonic disease
 * Human disease
 * DOID:10656
 * Colonic leiomyoma
 * colon lymphoma
 * class of disease
 * plump cancer lymphoma colorectal lymphoma
 * Human disease
 * DOID:1523
 * colon signet ring adenocarcinoma
 * class of disease
 * colon adenocarcinoma
 * Human disease
 * DOID:3033
 * colonic benign neoplasm
 * class of disease
 * intestinal benign neoplasm colonic neoplasm lymphangioma colonic disease
 * intestinal benign neoplasm that is located in the colon
 * DOID:235
 * colonic disease
 * class of disease
 * intestinal disease
 * pathological processes in the colon or large intestine
 * DOID:5353
 * C06.405.469.158
 * Diseases and disorders of colon
 * colonic lymphangioma
 * class of disease
 * colonic benign neoplasm
 * Human disease
 * DOID:10657
 * color agnosia
 * class of disease
 * agnosia visual agnosia
 * agnosia that is a loss of the ability to recognize a color, while being able to perceive or distinguish it
 * DOID:0060139
 * color blindness
 * class of disease
 * vision disorder colour vision deficiency blindness disease
 * inability or decreased ability to see colour, or perceive colour differences, under normal lighting conditions
 * DOID:13399
 * C10.597.751.941.256 C11.966.256 C23.888.592.763.941.256 C11.270.151.500
 * Color blindness
 * Ishihara 9.svg
 * colorectal adenocarcinoma
 * class of disease
 * colorectal carcinoma adenocarcinoma
 * colorectal cancer that derives from epithelial cells of glandular origin
 * DOID:0050861
 * Colorectal adenocarcinoma
 * colorectal adenoma
 * class of disease
 * colonic benign neoplasm gastrointestinal adenoma colorectal polyp intestinal benign neoplasm adenoma
 * human disease
 * DOID:0050860
 * C04.557.470.035.215
 * Colon cancer.jpg
 * colorectal cancer
 * class of disease
 * colorectal neoplasm large intestine cancer disease
 * cancer of the colon or rectum
 * DOID:9256
 * Colorectal cancer
 * Stomach colon rectum diagram-en.svg
 * colorectal carcinoma
 * class of disease
 * colorectal cancer carcinoma
 * colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa
 * DOID:0080199
 * columnar cell variant papillary carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:7088
 * combat disorder
 * class of disease
 * acute stress disorder post-traumatic stress disorder disease
 * acute stress disorder that involves neurotic reactions to unusual, severe, or overwhelming military stress
 * DOID:6950
 * F03.950.750.249
 * Combat stress reaction
 * combined T cell and B cell immunodeficiency
 * class of disease
 * combined immunodeficiency
 * human disease
 * DOID:628
 * combined cellular and humoral immune defects with granulomas
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0112253
 * combined oxidative phosphorylation deficiency 10
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111480
 * combined oxidative phosphorylation deficiency 11
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111481
 * combined oxidative phosphorylation deficiency 13
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111467
 * combined oxidative phosphorylation deficiency 14
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111477
 * combined oxidative phosphorylation deficiency 15
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111491
 * combined oxidative phosphorylation deficiency 16
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111469
 * combined oxidative phosphorylation deficiency 17
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111496
 * combined oxidative phosphorylation deficiency 18
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111484
 * combined oxidative phosphorylation deficiency 19
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111476
 * combined oxidative phosphorylation deficiency 2
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111483
 * combined oxidative phosphorylation deficiency 20
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111478
 * combined oxidative phosphorylation deficiency 21
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111465
 * combined oxidative phosphorylation deficiency 22
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111498
 * combined oxidative phosphorylation deficiency 23
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111500
 * combined oxidative phosphorylation deficiency 24
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111485
 * combined oxidative phosphorylation deficiency 27
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111489
 * combined oxidative phosphorylation deficiency 3
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111486
 * combined oxidative phosphorylation deficiency 31
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111488
 * combined oxidative phosphorylation deficiency 32
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111492
 * combined oxidative phosphorylation deficiency 33
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * DOID:0111495
 * combined oxidative phosphorylation deficiency 34
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111497
 * combined oxidative phosphorylation deficiency 35
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111464
 * combined oxidative phosphorylation deficiency 36
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111482
 * combined oxidative phosphorylation deficiency 37
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111499
 * combined oxidative phosphorylation deficiency 38
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111466
 * combined oxidative phosphorylation deficiency 39
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111475
 * combined oxidative phosphorylation deficiency 4
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111494
 * combined oxidative phosphorylation deficiency 40
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0112117
 * combined oxidative phosphorylation deficiency 41
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0112119
 * combined oxidative phosphorylation deficiency 42
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0112118
 * combined oxidative phosphorylation deficiency 43
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0112116
 * combined oxidative phosphorylation deficiency 45
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0112113
 * combined oxidative phosphorylation deficiency 46
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0112115
 * combined oxidative phosphorylation deficiency 47
 * class of disease
 * combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0112114
 * combined oxidative phosphorylation deficiency 48
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0112112
 * combined oxidative phosphorylation deficiency 49
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0112110
 * combined oxidative phosphorylation deficiency 5
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111473
 * combined oxidative phosphorylation deficiency 50
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0112111
 * combined oxidative phosphorylation deficiency 51
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0112137
 * combined oxidative phosphorylation deficiency 6
 * class of disease
 * combined oxidative phosphorylation deficiency X-linked recessive disease
 * human disease
 * DOID:0111502
 * combined oxidative phosphorylation deficiency 7
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111487
 * combined oxidative phosphorylation deficiency 8
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111479
 * combined oxidative phosphorylation deficiency 9
 * class of disease
 * autosomal recessive disease combined oxidative phosphorylation deficiency
 * human disease
 * DOID:0111472
 * combined thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:3281
 * comedocarcinoma
 * class of disease
 * intraductal carcinoma disease
 * carcinoma that is in situ
 * DOID:5670
 * commensal Klebsiella infectious disease
 * class of disease
 * klebsiellosis
 * Human disease
 * DOID:0050479
 * commensal bacterial infectious disease
 * class of disease
 * bacterial infectious disease
 * Human disease
 * DOID:0050339
 * common bile duct disease
 * class of disease
 * bile duct disease
 * Human disease
 * DOID:4137
 * C06.130.120.250
 * common bile duct neoplasm
 * class of disease
 * biliary tract neoplasm common bile duct disease
 * human disease
 * DOID:4608
 * C04.588.274.120.250.250 C06.130.120.120.280 C06.130.120.250.280 C06.130.320.120.280 C06.301.120.250.250
 * common peroneal nerve lesion
 * class of disease
 * mononeuritis of lower limb
 * Human disease
 * DOID:12527
 * common wart
 * class of disease
 * viral infectious disease wart
 * viral infectious disease that results in infection located in skin, has material basis in human papillomavirus (types 2 and 4)
 * DOID:11165
 * Verruca vulgaris
 * communicating hydrocephalus
 * class of disease
 * hydrocephalus
 * abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of impaired cerebrospinal fluid reabsorption by the arachnoid granulations
 * DOID:1573
 * compartment syndrome
 * class of disease
 * ischemia disease
 * condition in which increased pressure within one of the body&#39;s compartments results in insufficient blood supply to tissue within that space
 * DOID:682
 * C05.651.180 C14.907.303
 * Compartment syndrome
 * Fasciotomy leg.jpg
 * complement component 5 deficiency
 * class of disease
 * complement deficiency
 * Human disease
 * DOID:8158
 * complement component 6 deficiency
 * class of disease
 * complement deficiency
 * Human disease
 * DOID:0060299
 * complement component 7 deficiency
 * class of disease
 * complement deficiency
 * Human disease
 * DOID:0060300
 * complement deficiency
 * class of disease
 * primary immunodeficiency disease metabolic disease
 * primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation
 * DOID:626
 * Complement deficiencies
 * complete generalized lipodystrophy
 * class of disease
 * lipodystrophy
 * lipodystrophy that is characterized by complete loss of adipose tissue
 * DOID:0080298
 * complex cortical dysplasia with other brain malformations
 * class of disease
 * encephalopathy autosomal dominant disease
 * human disease
 * DOID:0090131
 * complex partial seizure
 * class of disease symptom or sign
 * focal epilepsy focal seizure
 * human disease
 * DOID:12382
 * C10.228.140.490.360.260
 * composite lymphoma
 * class of disease
 * B-cell lymphoma
 * lymphoma that begins in cells of the immune system in which different types of lymphoma cells occur at the same time
 * DOID:5820
 * C04.557.386.150 C04.557.435.295 C15.604.515.569.150 C20.683.515.761.150
 * conduct disorder
 * class of disease
 * specific developmental disorder behavioral disorder disease
 * specific developmental disorder marked by a pattern of repetitive behavior wherein the rights of others or social norms are violated
 * DOID:12995
 * F03.625.094.300
 * cone-rod dystrophy
 * class of disease
 * retinal degeneration monogenic disease
 * retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells
 * DOID:0050572
 * C11.270.152 C11.768.585.658.250 C16.320.290.152
 * cone-rod dystrophy 1
 * class of disease
 * cone-rod dystrophy
 * A cone-rod dystrophy that has material basis in variation in the chromosome region 18q21.1-q21.3.
 * DOID:0111009
 * cone-rod dystrophy 17
 * class of disease
 * cone-rod dystrophy
 * cone-rod dystrophy that has material basis in variation in the chromosome region 10q26
 * DOID:0111023
 * cone-rod dystrophy 8
 * class of disease
 * cone-rod dystrophy
 * cone-rod dystrophy that has material basis in variation in the chromosome region 1q12-q24
 * DOID:0111014
 * congenital Zika virus infection
 * class of disease
 * Zika virus infection vertically transmitted infection syndrome infectious embryofetopathy
 * human disease
 * DOID:0080180
 * congenital aphakia
 * class of disease
 * lens disease aphakia
 * Human disease
 * DOID:11367
 * congenital bile acid synthesis defect
 * class of disease
 * steroid inherited metabolic disorder bile acid synthesis defect with cholestasis and malabsorption congenital disorder
 * steroid inherited metabolic disorder characterized by abnormal conversion of cholesterol into bile acids which occurs predominantly in the liver
 * DOID:0050674
 * congenital chylothorax
 * class of disease
 * pleural disease chylothorax rare genetic respiratory disease primary interstitial lung disease specific to childhood due to alveolar vascular disorder
 * pleural disease characterized by the accumulation of chyle within the pleural space leading to respiratory distress, malnutrition and immunological compromise, either immediately after birth or within the first few weeks of life
 * DOID:0060646
 * congenital diarrhea
 * class of disease
 * diarrhea congenital disorder
 * diarrhea characterized by frequent loose or liquid bowel movements where the disease is present from birth
 * DOID:0060774
 * congenital disorder
 * class of disease
 * disease
 * condition present at birth regardless of cause; human disease or disorder developed prior to birth
 * DOID:0080015 DOID:0060035
 * C16
 * Congenital diseases and disorders
 * congenital disorder of glycosylation 1cc
 * class of disease
 * X-linked recessive disease congenital disorder of glycosylation type I
 * human disease
 * DOID:0111839
 * congenital disorder of glycosylation type I
 * class of disease
 * congenital disorder of glycosylation
 * congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor
 * DOID:0050570
 * congenital disorder of glycosylation type IIa
 * class of disease
 * congenital disorder of glycosylation type II autosomal recessive disease
 * A congenital disorder of glycosylation type II that has material basis in an autosomal recessive mutation of MGAT2 on chromosome 14q21.3.
 * DOID:0070253
 * congenital disorder of glycosylation type IIq
 * class of disease
 * congenital disorder of glycosylation type II autosomal recessive disease
 * A congenital disorder of glycosylation type II that has material basis in an autosomal recessive mutation of COG2 on chromosome 1q42.2.
 * DOID:0070269
 * congenital disorder of glycosylation type Ia
 * class of disease
 * congenital disorder of glycosylation type I autosomal recessive disease
 * human disease
 * DOID:0080552
 * congenital dyserythropoietic anemia type I
 * class of disease
 * congenital dyserythropoietic anemia
 * Congenital dyserythropoietic anemiatype I (CDA I) is a hematologic disorder of erythropoiesis characterized by moderate to severe macrocytic anemia occasionally associated with limb or nail deformities and scoliosis
 * DOID:0111396
 * congenital dyserythropoietic anemia type II
 * class of disease
 * congenital dyserythropoietic anemia autosomal recessive disease
 * medical condition
 * DOID:0111401
 * congenital dyserythropoietic anemia type III
 * class of disease
 * congenital dyserythropoietic anemia
 * medical condition
 * DOID:0111399
 * congenital dyserythropoietic anemia type IV
 * class of disease
 * congenital dyserythropoietic anemia autosomal dominant disease
 * medical condition
 * DOID:0111400
 * congenital dyserythropoietic anemia type Ia
 * class of disease
 * autosomal recessive disease congenital dyserythropoietic anemia type I
 * human disease
 * DOID:0111398
 * congenital dyserythropoietic anemia type Ib
 * class of disease
 * autosomal recessive disease congenital dyserythropoietic anemia type I
 * human disease
 * DOID:0111397
 * congenital fiber-type disproportion
 * class of disease
 * congenital myopathy
 * Human disease
 * DOID:0080102
 * Congenital fiber type disproportion
 * congenital fibrosarcoma
 * class of disease
 * pediatric fibrosarcoma
 * Human disease
 * DOID:8418
 * congenital generalized lipodystrophy type 1
 * class of disease
 * congenital generalized lipodystrophy
 * A congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of AGPAT2 on chromosome 9q34.3.
 * DOID:0111135
 * congenital granular cell tumor
 * class of disease
 * mesenchymal cell neoplasm
 * Human disease
 * DOID:8303
 * congenital heart block
 * class of disease
 * congenital heart disease genetic cardiac rhythm disease atrioventricular block heart conduction disease
 * atrioventricular block characterized by the presence of conduction system disease of any form, which is diagnosed on or before 28 days of life
 * DOID:990
 * congenital hemolytic anemia
 * class of disease symptom or sign
 * hemolytic anemia congenital anemia
 * Human disease
 * DOID:589
 * C15.378.071.141.150 C16.320.070
 * congenital hypogammaglobulinemia
 * class of disease
 * B cell deficiency agammaglobulinemia
 * Human disease
 * DOID:14177
 * congenital hypoplastic anemia
 * class of disease
 * aplastic anemia congenital anemia congenital bone marrow failure syndromes congenital disorder
 * Human disease
 * DOID:1342
 * C15.378.071.085.080 C15.378.190.223.500.500 C16.320.077
 * congenital hypothyroidism
 * class of disease
 * hypothyroidism congenital disorder
 * hypothyroidism that is present at birth
 * DOID:0050328
 * C05.116.099.343.347 C05.116.132.256 C16.320.240.625 C19.297.155 C19.874.482.281
 * Congenital hypothyroidism
 * Jaundice in newborn.jpg
 * congenital intrinsic factor deficiency
 * class of disease
 * vitamin B12 deficiency inborn disorder of cobalamin metabolism and transport vitamin B12 deficiency anemia congenital disorder
 * vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption
 * DOID:0050734
 * congenital lactase deficiency
 * class of disease
 * lactase deficiency carbohydrate metabolic disorder disorder of carbohydrate absorption and transport congenital intestinal disease due to an enzymatic defect metabolic disease with intestinal involvement autosomal recessive disease
 * rare severe gastrointestinal disorder in newborns primarily reported in Finland
 * DOID:0111646
 * congenital limbs-face contractures-hypotonia-developmental delay syndrome
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0081048
 * congenital megabladder
 * class of disease
 * bladder disease autosomal dominant disease Megacystis
 * human disease
 * DOID:0112014
 * congenital mesoblastic nephroma
 * class of disease
 * mesoblastic nephroma kidney cancer
 * Human disease
 * DOID:4773
 * congenital muscular dystrophy
 * class of disease
 * muscular dystrophy autosomal recessive disease disease
 * human disease
 * DOID:0050557
 * congenital muscular dystrophy 1B
 * class of disease
 * congenital muscular dystrophy genetic disease autosomal recessive disease
 * congenital muscular dystrophy characterized by autosomal recessive inheritance of proximal muscle weakness, muscle hypertrophy, and early respiratory failure that has material basis in variation in the chromosome region 1q42
 * DOID:0110634
 * congenital muscular dystrophy merosin-positive
 * class of disease
 * congenital muscular dystrophy genetic disease autosomal recessive disease
 * human disease
 * DOID:0110638
 * congenital muscular dystrophy with cataracts and intellectual disability
 * class of disease
 * congenital muscular dystrophy genetic disease autosomal recessive disease
 * human disease
 * DOID:0080197
 * congenital muscular dystrophy-dystroglycanopathy A14
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in in GMPPB on 3p21.31.
 * DOID:0111233
 * congenital muscular dystrophy-dystroglycanopathy A7
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in ISPD on 7p21.2-p21.1.
 * DOID:0111234
 * congenital muscular dystrophy-dystroglycanopathy type A
 * class of disease
 * muscular dystrophy-dystroglycanopathy
 * muscular dystrophy-dystroglycanopathy characterized by cobblestone lissencephaly, muscle weakness, and brain and eye anomalies that has material basis in autosomal recessive inheritance a defect in alpha-dystroglycan post-translational processing
 * DOID:0111229
 * congenital muscular dystrophy-dystroglycanopathy type A1
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMT1 on 9q34.13.
 * DOID:0111237
 * congenital muscular dystrophy-dystroglycanopathy type A10
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2.
 * DOID:0111239
 * congenital muscular dystrophy-dystroglycanopathy type A11
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3.
 * DOID:0111230
 * congenital muscular dystrophy-dystroglycanopathy type A12
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMK on 8p11.21.
 * DOID:0111235
 * congenital muscular dystrophy-dystroglycanopathy type A13
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in B4GAT1 on 11q13.2.
 * DOID:0111238
 * congenital muscular dystrophy-dystroglycanopathy type A3
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT1 on 1p34.1.
 * DOID:0111236
 * congenital muscular dystrophy-dystroglycanopathy type A5
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in FKRP on 19q13.32.
 * DOID:0111241
 * congenital muscular dystrophy-dystroglycanopathy type A6
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in LARGE on 22q12.3.
 * DOID:0111242
 * congenital muscular dystrophy-dystroglycanopathy type A8
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT2 on 3p22.1.
 * DOID:0111231
 * congenital muscular dystrophy-dystroglycanopathy type A9
 * class of disease
 * congenital muscular dystrophy-dystroglycanopathy type A
 * A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.
 * DOID:0111232
 * congenital myasthenic syndrome 10
 * class of disease
 * congenital myasthenic syndrome genetic disease autosomal recessive disease
 * human disease
 * DOID:0110668
 * congenital myasthenic syndrome 1A
 * class of disease
 * congenital myasthenic syndrome genetic disease autosomal dominant disease
 * human disease
 * DOID:0110663
 * congenital nongoitrous hypothryoidism 1
 * class of disease
 * hypothyroidism, congenital, nongoitrous genetic disease autosomal recessive disease
 * congenital hypothyroidism that has material basis in mutation in the TSHR gene on chromosome 14q31
 * DOID:0070126
 * congenital nongoitrous hypothryoidism 2
 * class of disease
 * hypothyroidism, congenital, nongoitrous congenital hypothyroidism due to developmental anomaly congenital thyroid malformation without hypothyroidism thyroid hormone resistance syndrome genetic disease autosomal dominant disease
 * congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13
 * DOID:0070124
 * congenital nongoitrous hypothryoidism 3
 * class of disease
 * hypothyroidism, congenital, nongoitrous genetic disease autosomal dominant disease
 * A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.
 * DOID:0070127
 * congenital nongoitrous hypothryoidism 4
 * class of disease
 * hypothyroidism, congenital, nongoitrous genetic disease autosomal recessive disease
 * congenital hypothyroidism characterized by a permanent thyroid deficiency present at birth and resulting from deficiency in TSH synthesis that has material basis in homozygous mutation in the TSHB gene on chromosome 1p13
 * DOID:0070123
 * congenital nongoitrous hypothryoidism 5
 * class of disease
 * hypothyroidism, congenital, nongoitrous genetic disease autosomal dominant disease congenital hypothyroidism
 * congenital hypothyroidism that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35
 * DOID:0070125
 * congenital nongoitrous hypothryoidism 6
 * class of disease
 * hypothyroidism, congenital, nongoitrous genetic disease autosomal dominant disease
 * A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.
 * DOID:0070128
 * congenital nongoitrous hypothyroidism 7
 * class of disease
 * autosomal recessive disease hypothyroidism, congenital, nongoitrous
 * human disease
 * DOID:0111836
 * congenital nongoitrous hypothyroidism 8
 * class of disease
 * autosomal dominant disease hypothyroidism, congenital, nongoitrous
 * human disease
 * DOID:0111837
 * congenital nongoitrous hypothyroidism 9
 * class of disease
 * X-linked recessive disease hypothyroidism, congenital, nongoitrous
 * human disease
 * DOID:0111835
 * congenital nystagmus 1
 * class of disease
 * autosomal genetic disease congenital nystagmus
 * human disease
 * DOID:0111790
 * congenital nystagmus 2
 * class of disease
 * congenital nystagmus autosomal dominant disease
 * human disease
 * DOID:0111792
 * congenital nystagmus 3
 * class of disease
 * autosomal dominant disease congenital nystagmus
 * human disease
 * DOID:0111793
 * congenital nystagmus 4
 * class of disease
 * congenital nystagmus autosomal dominant disease
 * human disease
 * DOID:0111794
 * congenital nystagmus 5
 * class of disease
 * X-linked dominant disease congenital nystagmus
 * human disease
 * DOID:0111796
 * congenital nystagmus 6
 * class of disease
 * congenital nystagmus
 * human disease
 * DOID:0111795
 * congenital nystagmus 7
 * class of disease
 * autosomal dominant disease congenital nystagmus
 * human disease
 * DOID:0111791
 * congenital ptosis
 * class of disease
 * ptosis
 * ptosis characterized by eyelid drop present at birth
 * DOID:0060261
 * congenital stationary night blindness
 * class of disease
 * hereditary night blindness
 * night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves
 * DOID:0050534
 * congenital stationary night blindness 1A
 * class of disease
 * congenital stationary night blindness X-linked recessive disease
 * A congenital stationary night blindness that has material basis in mutation in the NYX gene on chromosome Xp11.4.
 * DOID:0110870
 * congenital stationary night blindness 2A
 * class of disease
 * congenital stationary night blindness X-linked recessive disease
 * A congenital stationary night blindness that has material basis in mutation in the CACNA1F gene on chromosome Xp11.23.
 * DOID:0110871
 * congenital structural myopathy
 * class of disease
 * muscular disease
 * human disease
 * DOID:422
 * C05.651.575 C10.668.491.550
 * congenital symmetric circumferential skin creases 1
 * class of disease
 * autosomal dominant disease
 * human disease
 * DOID:0112242
 * congestive heart failure
 * class of disease
 * heart disease heart failure
 * human disease
 * DOID:6000
 * conidiobolomycosis
 * class of disease
 * subcutaneous mycosis
 * Human disease
 * DOID:0050279
 * conjugate gaze palsy
 * class of disease
 * strabismus disease
 * Human disease
 * DOID:12445
 * conjunctival cancer
 * class of disease
 * ocular cancer conjunctival neoplasm conjunctival disease
 * Human disease
 * DOID:5467
 * conjunctival concretion
 * class of disease
 * conjunctival deposit
 * Human disease
 * DOID:11988
 * conjunctival degeneration
 * class of disease
 * conjunctival disease conjunctival degenerations and deposits eye degenerative disease
 * Human disease
 * DOID:10139
 * conjunctival deposit
 * class of disease
 * conjunctival disease conjunctival degenerations and deposits
 * Human disease
 * DOID:11653
 * conjunctival disease
 * class of disease
 * eye disease
 * Human disease
 * DOID:4251
 * C11.187
 * conjunctival folliculosis
 * class of disease
 * acute conjunctivitis
 * Human disease
 * DOID:11219
 * conjunctival pigmentation
 * class of disease
 * pigmentation disorder
 * Human disease
 * DOID:12304
 * conjunctival pterygium
 * class of disease
 * conjunctival degeneration pterygium
 * human disease
 * DOID:10526
 * conjunctival vascular disease
 * class of disease
 * conjunctival disease
 * Human disease
 * DOID:10989
 * conjunctivochalasis
 * class of disease
 * conjunctival disease
 * Human disease
 * DOID:4250
 * Conjunctivochalasis
 * connective tissue benign neoplasm
 * class of disease
 * musculoskeletal system benign neoplasm connective tissue disease connective tissue neoplasm
 * musculoskeletal system benign neoplasm that is located in connective tissue
 * DOID:0060123
 * connective tissue disease
 * class of disease
 * musculoskeletal disorder skin and connective tissue diseases
 * musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage
 * DOID:65
 * C17.300
 * Connective tissue diseases
 * connective tissue neoplasm
 * class of disease
 * musculoskeletal system cancer connective tissue disease connective and soft tissue neoplasms
 * musculoskeletal system cancer that is located in connective tissue
 * DOID:201
 * C04.557.450.565 C17.300.680
 * constant exophthalmos
 * class of disease
 * orbital disease exophthalmos
 * Human disease
 * DOID:9945
 * constipation
 * class of disease symptom or sign
 * bowel dysfunction clinical sign feces and droppings symptom disease
 * bowel dysfunction that is characterized by infrequent or difficult evacuation of feces
 * DOID:2089
 * C23.888.821.150
 * Constipation
 * constrictive pericarditis
 * class of disease
 * pericarditis
 * heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function
 * DOID:11481
 * C14.280.720.595
 * Constrictive pericarditis
 * Constrictive pericarditis.jpg
 * contact blepharoconjunctivitis
 * class of disease
 * blepharoconjunctivitis
 * Human disease
 * DOID:13999
 * contact dermatitis
 * class of disease
 * dermatitis eczema disease
 * human disease
 * DOID:2773
 * C17.800.174.255 C17.800.815.255
 * Contact dermatitis
 * Contact dermatitis.jpg
 * contact lens corneal edema
 * class of disease
 * corneal edema
 * Human disease
 * DOID:11034
 * conus medullaris neoplasm
 * class of disease
 * Spinal cord cancer
 * Human disease
 * DOID:3641
 * conventional angiosarcoma
 * class of disease
 * angiosarcoma
 * Human disease
 * DOID:4512
 * conventional central osteosarcoma
 * class of disease
 * bone osteosarcoma
 * Human disease
 * DOID:3378
 * conventional fibrosarcoma
 * class of disease
 * fibrosarcoma
 * Human disease
 * DOID:3517
 * conventional leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5253
 * conventional malignant hemangiopericytoma
 * class of disease
 * hemangiopericytoma hemangiopericytoma, malignant
 * Human disease
 * DOID:6197
 * conversion disorder
 * class of disease symptom or sign
 * somatoform disorder functional neurologic disorder disease
 * physical illness or symptoms caused by serious emotional stress
 * DOID:1768
 * F03.875.300
 * cor pulmonale
 * class of disease
 * congestive heart failure disease
 * human disease
 * DOID:8515
 * C14.280.832
 * Pulmonary heart disease
 * core binding factor acute myeloid leukemia
 * class of disease
 * acute myeloid leukemia
 * human disease
 * DOID:0080796
 * cork-handlers' disease
 * class of disease
 * extrinsic allergic alveolitis
 * An extrinsic allergic alveolitis caused by inhalation of cork dust containing the antigens produced by the fungus Penicillium glabrum. The symptoms include dyspnea, wheezing cough, fever and asthenia.
 * DOID:840
 * cornea cancer
 * class of disease
 * ocular cancer cornea neoplasm corneal disease
 * Human disease
 * DOID:6199
 * cornea plana
 * class of disease
 * corneal disease
 * Human disease
 * DOID:0060287
 * cornea squamous cell carcinoma
 * class of disease
 * cornea cancer squamous cell carcinoma
 * Human disease
 * DOID:13538
 * corneal abscess
 * class of disease
 * deep keratitis
 * Human disease
 * DOID:11543
 * corneal argyrosis
 * class of disease
 * corneal disease argyria
 * Human disease
 * DOID:13447
 * corneal degeneration
 * class of disease
 * corneal disease eye degenerative disease
 * Human disease
 * DOID:1237
 * corneal deposit
 * class of disease
 * corneal disease
 * Human disease
 * DOID:11547
 * corneal disease
 * class of disease
 * eye disease
 * human disease
 * DOID:10124
 * C11.204
 * Disorders of sclera and cornea
 * corneal dystrophy
 * class of disease
 * corneal disease
 * human disease
 * DOID:2566
 * C11.204.236 C11.270.162 C16.320.290.162
 * Corneal dystrophy
 * corneal ectasia
 * class of disease
 * corneal disease
 * Human disease
 * DOID:1436
 * corneal edema
 * class of disease
 * corneal disease
 * Human disease
 * DOID:11030
 * C11.204.267
 * corneal endothelial dystrophy
 * class of disease
 * corneal dystrophy
 * Human disease
 * DOID:0060443
 * corneal granular dystrophy
 * class of disease
 * epithelial-stromal TGFBI dystrophy autosomal dominant disease
 * Human disease
 * DOID:12318
 * Granular corneal dystrophy
 * corneal neovascularization
 * class of disease
 * keratitis neovascularization
 * Human disease
 * DOID:11382
 * C11.204.290
 * Corneal neovascularization
 * corneal opacification and other ocular anomalies
 * class of disease
 * sclerocornea genetic disease monogenic disease eye disease
 * sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis
 * DOID:0060648
 * corneal staphyloma
 * class of disease
 * corneal disease staphyloma
 * Human disease
 * DOID:12753
 * corneal ulcer
 * class of disease symptom or sign
 * keratitis corneal disease eye ulceration cornea symptom disease
 * area of epithelial tissue loss from corneal surface; associated with inflammatory cells in the cornea and anterior chamber
 * DOID:8463
 * C01.539.375.177 C11.204.564.225 C11.294.177
 * Corneal ulcer
 * coronary aneurysm
 * class of disease
 * aneurysm aneurysm of heart coronary artery disease
 * Human disease
 * DOID:3362
 * C14.280.647.250.250 C14.907.055.395 C14.907.585.250.250
 * Coronary aneurysm
 * coronary artery anomaly
 * class of disease
 * coronary artery disease vascular malformation congenital heart disease
 * Human disease
 * DOID:11843
 * C14.240.400.210 C14.280.400.210 C16.131.240.400.210
 * Coronary artery anomalies
 * coronary artery disease
 * class of disease
 * artery disease cardiovascular disease disease
 * disease characterized by plaque building up in the arteries of the heart
 * DOID:3393
 * C14.280.647.250.260 C14.907.137.126.339 C14.907.585.250.260
 * Coronary artery disease
 * Blausen 0257 CoronaryArtery Plaque.png
 * coronary artery vasospasm
 * class of disease
 * coronary artery disease vasospasm disease
 * Human disease
 * DOID:11840
 * C14.280.647.250.295 C14.907.585.250.295
 * coronary restenosis
 * class of disease
 * coronary stenosis restenosis
 * Human disease
 * DOID:4247
 * C14.280.647.250.285.200 C14.907.585.250.285.200
 * coronary stenosis
 * class of disease
 * coronary artery disease
 * Human disease
 * DOID:4248
 * C14.280.647.250.285 C14.907.585.250.285
 * coronary thrombosis
 * class of disease
 * coronary artery disease thrombosis arterial thrombosis disease
 * disease: formation of a blood clot inside a blood vessel of the heart, which clot may then restrict blood flow within the heart, leading to heart tissue damage, or a myocardial infarction, also known as a heart attack
 * DOID:11847
 * C14.280.647.250.290 C14.907.355.830.220 C14.907.585.250.290
 * Cardiac thrombosis
 * corpus callosum lipoma
 * class of disease
 * cerebral hemisphere lipoma
 * Human disease
 * DOID:6294
 * corpus callosum oligodendroglioma
 * class of disease
 * brain oligodendroglioma oligodendroglioma
 * brain oligodendroglioma located in the corpus callosum
 * DOID:0050901
 * corpus luteum cyst
 * class of disease
 * ovarian cyst
 * human disease
 * DOID:13050
 * cortical deafness
 * class of disease
 * sensorineural hearing loss agnosia central auditory disease auditory agnosia
 * agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact
 * DOID:0060140
 * cortical senile cataract
 * class of disease
 * senile cataract
 * human disease
 * DOID:13574
 * cortical thymoma
 * class of disease
 * dendritic cell thymoma
 * Human disease
 * DOID:6530
 * corticosteroid allergy
 * class of disease
 * drug allergy steroids allergy
 * drug allergy that has allergic trigger corticosteroid
 * DOID:0040014
 * corticosterone methyloxidase deficiency 1
 * class of disease
 * autosomal recessive disease adrenal gland disease
 * human disease
 * DOID:0080626
 * cortisone reductase deficiency
 * class of disease
 * endocrine system disease hyperandrogenism
 * endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism
 * DOID:0090139
 * costochondritis
 * class of disease
 * chondropathy syndrome disease
 * human disease
 * DOID:14021
 * cough variant asthma
 * class of disease
 * asthma chronic asthma
 * asthma that is characterized by chronic nonproductive cough without shortness of breath
 * DOID:12323
 * C08.127.108.784 C08.381.495.108.750 C08.674.095.784 C20.543.480.680.095.688
 * cow milk allergy
 * class of disease
 * milk allergy
 * milk allergy triggered by Bos taurus milk
 * DOID:0060521
 * cranial nerve III tumor
 * class of disease
 * third cranial nerve disease cranial nerve neoplasm peripheral nervous system neoplasm
 * Human disease
 * DOID:2817
 * cranial nerve disease
 * class of disease
 * peripheral neuropathy
 * neuropathy that is located in one of the twelve cranial nerves
 * DOID:5656
 * C10.292
 * cranial nerve neoplasm
 * class of disease
 * nervous system neoplasm cranial nerve disease central nervous system cancer
 * Human disease
 * DOID:338
 * C04.588.614.300 C04.588.614.596.240 C10.292.225 C10.551.360 C10.551.775.250
 * Cranial nerve neoplasms
 * cranial nerve palsy
 * class of disease symptom or sign
 * cranial nerve disease palsy eye symptom
 * Human disease
 * DOID:3817
 * cranial pseudosarcomatous fasciitis
 * class of disease
 * pseudosarcomatous fibromatosis
 * Human disease
 * DOID:7326
 * cranio-facial dystonia
 * class of disease
 * focal dystonia
 * focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck
 * DOID:0050845
 * craniodiaphyseal dysplasia
 * class of disease
 * osteosclerosis
 * osteosclerosis that results in increased calcium concentration located in skull which decreases the size of cranium foramina and cervical spinal canal
 * DOID:0080032
 * cranioectodermal dysplasia 1
 * class of disease
 * Sensenbrenner syndrome
 * human disease
 * DOID:0080803
 * cranioectodermal dysplasia 2
 * class of disease
 * Sensenbrenner syndrome
 * human disease
 * DOID:0080804
 * cranioectodermal dysplasia 3
 * class of disease
 * Sensenbrenner syndrome
 * human disease
 * DOID:0080805
 * cranioectodermal dysplasia 4
 * class of disease
 * Sensenbrenner syndrome
 * human disease
 * DOID:0080806
 * craniopharyngioma
 * class of disease
 * central nervous system organ benign neoplasm Rathke's pouch tumor
 * type of brain tumor derived from pituitary gland embryonic tissue that occurs most commonly in children, but also affects adults
 * DOID:3840
 * C04.557.465.625.200 C04.557.580.625.200
 * Craniopharyngiomas
 * Adamantinomatous craniopharyngioma - very low mag.jpg
 * craniosynostosis
 * class of disease
 * synostosis rare disease craniofacial disease disease
 * premature fusion of bones in the skull
 * DOID:2340
 * C05.116.099.370.894.232 C05.660.207.240 C05.660.906.364 C16.131.621.207.240 C16.131.621.906.364
 * Craniosynostosis
 * Cranialsynostosis.jpg
 * crater-like holes of optic disc
 * class of disease
 * visual pathway disease
 * Human disease
 * DOID:13295
 * Optic pit
 * crescentic glomerulonephritis
 * class of disease
 * acute proliferative glomerulonephritis
 * Human disease
 * DOID:13139
 * cribriform carcinoma
 * class of disease
 * breast carcinoma
 * Human disease
 * DOID:5675
 * cribriform variant testicular seminoma
 * class of disease
 * testis seminoma
 * Human disease
 * DOID:7269
 * critical illness polyneuropathy
 * class of disease
 * inflammatory and toxic neuropathy polyneuropathy
 * Human disease
 * DOID:14402
 * crustacean allergy
 * class of disease
 * shellfish allergy seafood allergy
 * shellfish allergy triggered by Crustacea
 * DOID:0060524
 * cryptococcal meningitis
 * class of disease
 * cryptococcosis fungal meningitis
 * fungal meningitis that has material basis in Crypococcus fungal infection
 * DOID:0080159 DOID:12052
 * C01.150.703.181.500.500 C01.150.703.248.290 C10.228.228.198.500.500 C10.586.625.300.500 C01.207.198.500.500
 * Meningeal cryptococcosis
 * cryptophthalmos
 * class of disease
 * eyelid disease congenital disorder
 * congenital abnormality characterized by the presence of a continuous layer of skin extending over the eyeballs and the absence of eyelids and the palpebral fissure
 * DOID:0111716
 * cryptorchidism
 * class of disease
 * congenital disorder testicular disease male reproductive system disease genetic disease sex differentiation disease disease
 * defective mammal development
 * DOID:11383
 * C12.200.294.829.258 C12.200.706.258 C16.131.939.258 C19.391.829.258 C12.100.500.829.258 C12.800.258
 * Cryptorchidism
 * cutaneous Paget's disease
 * class of disease
 * skin carcinoma extramammary Paget's disease
 * skin carcinoma that is characterized by infiltration of the skin by neoplastic large cells with abundant pale cytoplasm and large nuclei with prominent nucleoli
 * DOID:3450
 * cutaneous T cell lymphoma
 * class of disease
 * peripheral T-cell lymphoma genetic disease cutaneous lymphoma disease
 * non-Hodgkin&#39;s lymphoma that has material basis in a mutation of T cells
 * DOID:0060061
 * C04.557.386.480.750.800 C15.604.515.569.480.750.800 C20.683.515.761.480.750.800
 * Cutaneous T-cell lymphoma
 * cutaneous candidiasis
 * class of disease symptom or sign
 * dermatomycosis candidiasis skin disease
 * candidiasis that is characterized by Candida infection located in the skin
 * DOID:0080161
 * C01.150.703.160.132 C01.150.703.302.105 C01.800.200.105 C17.800.838.208.170
 * Candidiasis of the skin
 * cutaneous diphtheria
 * class of disease
 * pyoderma diphtheria
 * pyoderma that is a milder form of diphtheria restricted to the skin producing shallow skin ulcers is caused by direct physical contact of individuals infected with Corynebacterium diphtheriae as the bacteria releases the diphtheria toxin
 * DOID:12275
 * cutaneous endometriosis
 * class of disease
 * endometriosis
 * human disease
 * DOID:11430
 * cutaneous ganglioneuroma
 * class of disease
 * skin benign neoplasm ganglioneuroma
 * Human disease
 * DOID:2425
 * cutaneous leiomyosarcoma
 * class of disease
 * skin sarcoma
 * Human disease
 * DOID:5273
 * Cutaneous leiomyosarcoma
 * cutaneous liposarcoma
 * class of disease
 * skin sarcoma
 * Human disease
 * DOID:5712
 * cutaneous lupus erythematosus
 * class of disease
 * lupus erythematosus skin disease
 * lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight
 * DOID:0050169
 * C17.300.475 C17.800.480
 * cutaneous mastocytosis
 * class of disease
 * mastocytosis skin disease
 * human disease
 * DOID:3663
 * C04.557.450.565.465.500 C17.800.508.473
 * cutaneous meningioma
 * class of disease
 * skin benign neoplasm ectopic meningioma skin cancer
 * Human disease
 * DOID:8006
 * cutaneous mucoepidermoid carcinoma
 * class of disease
 * skin benign neoplasm mucoepidermoid carcinoma skin carcinoma
 * Human disease
 * DOID:4683
 * cutaneous small-vessel vasculitis
 * class of disease
 * hypersensitivity vasculitis skin disease microvasculitis allergy disease
 * hypersensitivity vasculitis that results in inflammation of small blood vessels, characterized clinically by palpable purpura, which is a slightly elevated purpuric rash over one or more areas of the skin
 * DOID:11450
 * Cutaneous small-vessel vasculitis
 * cutaneous squamous-cell carcinoma
 * class of disease
 * skin carcinoma squamous cell carcinoma disease
 * skin carcinoma that has material basis in squamous cells
 * DOID:3151
 * Squamous-cell carcinoma of the skin
 * cyclophosphamide allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger cyclophosphamide
 * DOID:0040027
 * cycloplegia
 * class of disease
 * eye accommodation disease disease
 * paralysis of the ciliary muscle of the eye, resulting in a loss of accommodation
 * DOID:10033
 * cyclothymia
 * class of disease
 * bipolar disorder disease
 * persistent instability of mood that involves recurrent hypomanic and dysthymic episodes, but no full manic episodes or full major depressive episodes
 * DOID:845
 * F03.600.500
 * cyclotropia
 * class of disease
 * strabismus
 * Human disease
 * DOID:9838
 * cylindrical spirals myopathy
 * class of disease
 * congenital myopathy
 * Human disease
 * DOID:0080103
 * cystadenocarcinoma
 * class of disease
 * cystic neoplasm malignant cystadenoma disease
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, in which cystic accumulations of retained secretions are formed
 * DOID:3111
 * C04.557.470.200.025.480 C04.557.470.590.480
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * cystadenofibroma
 * class of disease
 * adenofibroma ovarian benign neoplasm
 * adenofibroma composed of epithelial ovarian tissue
 * DOID:5482
 * C04.557.450.565.590.595.050.500 C04.557.470.590.482 C04.557.470.625.050.500
 * cystadenoma
 * class of disease
 * adenoma
 * adenoma that is a cystic
 * DOID:2634
 * C04.557.470.035.320 C04.557.470.590.485
 * Cystadenomas
 * Pancreatic serous cystadenoma - high mag.jpg
 * cystathioninuria
 * class of disease
 * sulfuraminoacidemia amino acid metabolic disorder genetic disease
 * amino acid metabolic disorder characterized by elevated plasma and urinary cystathionine levels that has material basis in homozygous or compound heterozygous mutation in the CTH gene on chromosome 1p31
 * DOID:0090142
 * cystic basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4302
 * cystic echinococcosis
 * class of disease
 * echinococcosis lung disease bone disease heart disease liver disease encephalopathy
 * Human disease
 * DOID:1495
 * Hydatid cyst.JPG
 * cystic kidney disease
 * class of disease
 * renal cyst kidney disease
 * congenital or acquired kidney disorder characterized by the presence of renal cysts
 * DOID:2975
 * C12.777.419.403 C13.351.968.419.403
 * Cystic kidney diseases
 * cystic lymphangioma
 * class of disease
 * lymphangioma Cystic lymphatic malformation hygroma
 * human disease
 * DOID:3081
 * C04.557.375.450.450
 * Cystic hygroma
 * cystic nephroma
 * class of disease
 * kidney benign neoplasm nephroma disease
 * Human disease
 * DOID:2673
 * Cystic nephroma
 * cystic teratoma
 * class of disease
 * teratoma benign teratoma
 * Human disease
 * DOID:2660
 * cystinuria
 * class of disease
 * amino acid metabolic disorder ureteral disease bladder disease kidney disease disease
 * amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder
 * DOID:9266
 * C12.777.419.815.885.250 C13.351.968.419.815.885.250 C16.320.565.861.885.250 C18.452.648.861.885.250
 * Cystine crystals in urine
 * cystitis
 * class of disease symptom or sign
 * bladder disease inflammation inflammatory disease disease
 * human disease
 * DOID:1679
 * C12.200.777.829.495 C12.050.351.968.829.495 C12.950.829.495
 * Cystitis
 * Diverse e Coli.png
 * cystitis cystica
 * class of disease
 * cystitis
 * human disease
 * DOID:7138
 * Cystitis cystica
 * cystoid macular edema
 * class of disease
 * macular retinal edema
 * Human disease
 * DOID:4447
 * cystoid macular retinal degeneration
 * class of disease
 * degeneration of macula and posterior pole
 * Human disease
 * DOID:14245
 * cytochrome P450 oxidoreductase deficiency
 * class of disease
 * steroid inherited metabolic disorder autosomal recessive disease
 * human disease
 * DOID:0080925
 * cytomegalovirus retinitis
 * class of disease
 * cytomegaloviral disease retinitis viral eye infection disease
 * retinitis that has material basis in Cytomegalovirus
 * DOID:0080160
 * C01.375.725.270 C01.925.256.466.245.150 C11.294.800.270 C11.768.773.360 C01.925.325.270
 * Cytomegalovirus retinitis
 * Fundus photograph-CMV retinitis EDA07.JPG
 * dacryoadenitis
 * class of disease
 * lacrimal apparatus disease disease
 * human disease
 * DOID:950
 * Tear system.svg
 * dacryocystitis
 * class of disease
 * acute inflammation of lacrimal passage disease
 * infection of the lacrimal sac
 * DOID:9938
 * C11.496.221
 * Dacryocystitis
 * dacryocystocele
 * class of disease
 * chronic inflammation of lacrimal passage
 * Human disease
 * DOID:9939
 * deafness, aminoglycoside-induced
 * class of disease
 * drug-induced hearing loss
 * human disease
 * DOID:0111734
 * dedifferentiated liposarcoma
 * class of disease
 * liposarcoma
 * liposarcoma that is characterized as a high-grade tumor that occurs when a lower-grade tumor changes and creates new high-grade cells
 * DOID:0080531
 * deep angioma
 * class of disease
 * hemangioma
 * Human disease
 * DOID:469
 * deep corneal vascularisation
 * class of disease
 * corneal neovascularization
 * Human disease
 * DOID:12087
 * deep keratitis
 * class of disease
 * keratitis
 * human disease
 * DOID:9858
 * deep leiomyoma
 * class of disease
 * leiomyoma
 * Human disease
 * DOID:5128
 * deficiency anemia
 * class of disease
 * anemia nutritional deficiency disease
 * Human disease
 * DOID:13121
 * Nutritional anemias
 * degeneration of macula and posterior pole
 * class of disease
 * macular degeneration
 * human disease
 * DOID:2007
 * degenerative disc disease
 * class of disease
 * Intervertebral disc disorder bone deterioration disease
 * bone deterioration disease that has material basis in gradual dehydration and tears located in intervertebral disc
 * DOID:90
 * C05.116.900.153
 * Degenerative disc disease
 * Cervical Spine MRI showing degenerative changes closeup.jpg
 * degenerative myopia
 * class of disease
 * eye degenerative disease myopia
 * Excessive axial myopia associated with complications (especially posterior staphyloma and choroidal neovascularization) that can lead to blindness
 * DOID:11829
 * C11.744.636.500
 * dehydrated hereditary stomatocytosis
 * class of disease
 * hereditary stomatocytosis hemolytic anemia
 * DOID:0111575
 * dehydrated hereditary stomatocytosis 1
 * class of disease
 * dehydrated hereditary stomatocytosis autosomal dominant disease
 * human disease
 * DOID:0111576
 * dehydration polycythemia
 * class of disease
 * acquired polycythemia hemoconcentration
 * Human disease
 * DOID:2833
 * delayed sleep phase disorder
 * class of disease
 * sleep disorder circadian rhythm sleep disorder disease
 * chronic mismatch between a person&#39;s normal daily rhythm, compared to other people and societal norms
 * DOID:0111141
 * delta chain disease
 * class of disease
 * heavy chain disease
 * heavy chain disease that results from an overproduction of delta antibody (IgD)
 * DOID:0060129
 * delta thalassemia
 * class of disease
 * thalassemia beta thalassemia autosomal dominant disease
 * type of thalassemia
 * DOID:0080773
 * C15.378.071.141.150.875.575 C15.378.420.826.200 C16.320.070.875.575 C16.320.365.826.575
 * delusional disorder
 * class of disease symptom or sign
 * psychosis disease
 * mental disease
 * DOID:778
 * dementia
 * class of disease symptom or sign
 * cognitive disorder organic brain syndrome clinical sign disability affecting intellectual abilities disease
 * long-term brain disorder causing personality changes and impaired memory, reasoning, and social function
 * DOID:1307
 * C10.228.140.380 F03.615.400
 * Dementia
 * [[File:An old man diagnosed as suffering from senile dementia. Colo Wellcome L0026689.jpg|center|64px]]
 * demyelinating disease
 * class of disease
 * neurological disorder neurodegeneration central nervous system disease disease
 * type of neurological disease where the myelin sheath of neurons is damaged
 * DOID:3213
 * C10.314
 * Demyelinating diseases
 * MS Demyelinisation CD68 10xv2.jpg
 * demyelinating polyneuropathy
 * class of disease
 * polyneuropathy spinal cord disease demyelinating disease
 * Polyneuropathy that is characterized by demyelination of axons
 * DOID:5214
 * dendritic cell deficiency
 * class of disease
 * primary immunodeficiency disease
 * human disease
 * DOID:0111963
 * dendritic cell sarcoma
 * class of disease
 * histiocytic and dendritic cell cancer sarcoma dendritic cell tumor
 * histiocytic and dendritic cell cancer that is mainly located in lymph nodes
 * DOID:7849
 * dendritic cell thymoma
 * class of disease
 * thymoma leukocyte disease hematologic cancer
 * Human disease
 * DOID:3282
 * dengue shock syndrome
 * class of disease
 * dengue fever dengue hemorrhagic fever
 * Human disease
 * DOID:0050125
 * dental abscess
 * class of disease symptom or sign
 * tooth pathology abscess
 * tooth disease characterized by a localized collection of pus associated with a tooth
 * DOID:0060324
 * Tooth abscess
 * Abces parulique.jpg
 * dental caries
 * class of disease
 * teeth hard tissue disease caries
 * deformation of teeth made by acids from bacteria
 * DOID:216
 * C07.793.720.210
 * Dental caries
 * Tooth model.jpg
 * dental enamel hypoplasia
 * class of disease
 * teeth hard tissue disease
 * Human disease
 * DOID:693
 * C07.650.800.255 C07.793.700.255 C16.131.850.800.255
 * Enamel hypoplasia
 * 법랑질저형성증.jpg
 * dental fluorosis
 * class of disease
 * tooth pathology fluoride toxicity disease
 * human disease
 * DOID:13711
 * C07.793.330
 * Dental fluorosis
 * Dental Flurosis (teeth with brown stains).jpg
 * dental pulp calcification
 * class of disease
 * dental pulp disease
 * Human disease
 * DOID:5608
 * C07.793.237.252
 * dental pulp disease
 * class of disease
 * tooth pathology connective tissue disease
 * disease involving the dental pulp
 * DOID:5330
 * C07.793.237
 * dental pulp necrosis
 * class of disease
 * dental pulp disease
 * Human disease
 * DOID:11623
 * C07.793.237.315 C23.550.717.182
 * dentin caries
 * class of disease
 * dental caries
 * Human disease
 * DOID:10461
 * dentine erosion
 * class of disease
 * dental erosion
 * Human disease
 * DOID:13629
 * dentine hypersensitivity
 * class of disease
 * orofacial pain teeth hard tissue disease
 * Human disease
 * DOID:698
 * C07.793.266
 * denture stomatitis
 * class of disease
 * stomatitis
 * lip disease
 * DOID:11875
 * C07.465.864.875
 * dependent personality disorder
 * class of disease
 * personality disorder dependency disease
 * personality disorder that is characterized by a pervasive psychological dependence on other people
 * DOID:10931
 * F03.675.200
 * Dependent personality disorder
 * depersonalization disorder
 * class of disease
 * dissociative disorder depersonalization
 * dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization
 * DOID:11038
 * dermal unilateral segmental cavernous angioma
 * class of disease
 * cavernous hemangioma
 * Human disease
 * DOID:3148
 * dermatitis
 * class of disease symptom or sign
 * skin disease skin and integumentary tissue symptom disease
 * inflammation of the skin
 * DOID:2723
 * C17.800.174
 * Dermatitis
 * Dermatitis2015.jpg
 * dermatitis herpetiformis
 * class of disease symptom or sign
 * autoimmune skin disease bullous skin disease pemphigoid disease
 * human disease
 * DOID:8505
 * C17.800.174.360 C17.800.865.360 C20.111.318
 * Dermatitis herpetiformis
 * dermatographia
 * class of disease
 * physical urticaria disease
 * human skin condition, responsible for "skin writing" effect in those affected
 * DOID:743
 * Dermatographic urticaria
 * Dermographism in child.jpg
 * dermatomycosis
 * class of disease
 * skin disease fungal infectious disease skin infection
 * cutaneous mycosis that results in fungal infection located in skin or of its appendages, has material basis in Ascomycota fungi other than the dermatophytes
 * DOID:1563 DOID:0050134
 * C01.150.703.302 C01.800.200 C17.800.838.208
 * dermatosis papulosa nigra
 * class of disease
 * dermatitis seborrheic keratosis
 * Human disease
 * DOID:4400
 * Dermatosis papulosa nigra
 * dermis tumor
 * class of disease
 * skin benign neoplasm
 * Human disease
 * DOID:2438
 * dermoid cyst
 * class of disease
 * cystic teratoma disease
 * tissue disease
 * DOID:2658
 * C04.182.201 C04.557.465.910.250
 * Dermoid cysts
 * Dermoid cyst intracranial.jpg
 * dermoid cyst of ovary
 * class of disease
 * ovarian cyst ovarian cancer dermoid cyst ovarian benign neoplasm
 * Human disease
 * DOID:5117
 * Ovarian dermoid cysts
 * dermoid cyst of skin
 * class of disease
 * skin cancer skin benign neoplasm dermoid cyst
 * Human disease
 * DOID:13691
 * descending colon cancer
 * class of disease
 * plump cancer
 * Human disease
 * DOID:12190
 * desmoid disease, hereditary
 * class of disease
 * aggressive fibromatosis syndrome autosomal genetic disease
 * desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential
 * DOID:0111349
 * desmoplastic small-round-cell tumor
 * class of disease
 * soft-tissue sarcoma sarcoma
 * aggressive, rare cancer
 * DOID:6785
 * C04.557.450.795.315
 * Desmoplastic small round cell tumour
 * detrusor sphincter dyssynergia
 * class of disease
 * neurogenic bladder bladder disease
 * Human disease
 * DOID:12145
 * deuteranopia
 * class of disease
 * congenital color blindness color blindness red–green color blindness dichromatopsia
 * human disease, green color blindness
 * DOID:13909
 * Deuteranopia
 * developmental and epileptic encephalopathy
 * class of disease
 * electroclinical syndrome
 * human disease
 * DOID:0112202
 * developmental and epileptic encephalopathy 100
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070386
 * developmental and epileptic encephalopathy 101
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070387
 * developmental and epileptic encephalopathy 102
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070388
 * developmental and epileptic encephalopathy 103
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070389
 * developmental and epileptic encephalopathy 104
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070390
 * developmental and epileptic encephalopathy 108
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070394
 * developmental and epileptic encephalopathy 109
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070378
 * developmental and epileptic encephalopathy 110
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0070395
 * developmental and epileptic encephalopathy 67
 * class of disease
 * developmental and epileptic encephalopathy autosomal dominant disease
 * human disease
 * DOID:0112203
 * developmental and epileptic encephalopathy 68
 * class of disease
 * autosomal recessive disease developmental and epileptic encephalopathy
 * human disease
 * DOID:0112204
 * developmental and epileptic encephalopathy 69
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112205
 * developmental and epileptic encephalopathy 70
 * class of disease
 * autosomal dominant disease developmental and epileptic encephalopathy
 * human disease
 * DOID:0112206
 * developmental and epileptic encephalopathy 71
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112207
 * developmental and epileptic encephalopathy 72
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112208
 * developmental and epileptic encephalopathy 73
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112209
 * developmental and epileptic encephalopathy 74
 * class of disease
 * developmental and epileptic encephalopathy autosomal dominant disease
 * human disease
 * DOID:0112210
 * developmental and epileptic encephalopathy 75
 * class of disease
 * developmental and epileptic encephalopathy autosomal recessive disease
 * human disease
 * DOID:0112211
 * developmental and epileptic encephalopathy 78
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112214
 * developmental and epileptic encephalopathy 79
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112215
 * developmental and epileptic encephalopathy 80
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112216
 * developmental and epileptic encephalopathy 81
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112217
 * developmental and epileptic encephalopathy 83
 * class of disease
 * autosomal recessive disease developmental and epileptic encephalopathy
 * human disease
 * DOID:0112218
 * developmental and epileptic encephalopathy 84
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112219
 * developmental and epileptic encephalopathy 89
 * class of disease
 * developmental and epileptic encephalopathy
 * human disease
 * DOID:0112223
 * developmental coordination disorder
 * class of disease
 * motor disorder specific developmental disorder disease
 * neurodevelopmental condition
 * DOID:9923
 * F03.625.813
 * Dyspraxia
 * developmental delay and seizures with or without movement abnormalities
 * class of disease
 * syndromic intellectual disability
 * human disease
 * DOID:0080473
 * developmental disorder
 * class of disease
 * mental disorder developmental disability neurodevelopmental disorder disease
 * disease of mental health that occur during a child&#39;s developmental period between birth and age 18 resulting in retarding of the child&#39;s psychological or physical development
 * DOID:0060037
 * dextro-looped transposition of the great arteries 1
 * class of disease
 * dextro-transposition of the great arteries genetic disease autosomal dominant disease
 * dextro-looped transposition of the great arteries that has material basis in heterozygous missense mutation in the MED13L gene on chromosome 12q24
 * DOID:0060771
 * dextrocardia
 * class of disease
 * heart position anomaly congenital heart disease disease
 * rare congenital defect in which the apex of the heart is located on the right side of the body
 * DOID:9565
 * C14.240.400.280 C14.280.400.280 C16.131.240.400.280 C16.131.810.250
 * Dextrocardia
 * Situs inversus chest Nevit.jpg
 * diabetes
 * class of disease
 * glucose metabolism disease disease
 * group of metabolic disorders characterized by high blood sugar levels over a prolonged period
 * DOID:9351
 * C18.452.394.750 C19.246
 * Diabetes mellitus
 * Blue circle for diabetes.svg
 * diabetes
 * class of disease
 * glucose metabolism disease
 * human disease
 * DOID:0081062
 * diabetic angiopathy
 * class of disease
 * peripheral vascular disease complications of diabetes mellitus
 * human disease
 * DOID:11713
 * C14.907.320 C19.246.099.500
 * Diabetic angiopathy
 * diabetic autonomic neuropathy
 * class of disease
 * autonomic neuropathy diabetic neuropathy
 * Autonomic neuropathy that is caused by diabetes mellitus
 * DOID:11503
 * diabetic cataract
 * class of disease
 * cataract ocular manifestation of diabetes
 * Human disease
 * DOID:13328
 * diabetic encephalopathy
 * class of disease
 * encephalopathy complications of diabetes mellitus
 * brain disease that is characterized by functional impairment of cognition, cerebral signal conduction, neurotransmission and synaptic plasticity, and underlying structural pathology associated with diabetes
 * DOID:0050850
 * diabetic ketoacidosis
 * class of disease
 * complications of diabetes mellitus type 2 diabetes ketoacidosis metabolic acidosis disease
 * potentially life-threatening complication in people with diabetes mellitus
 * DOID:1837 DOID:10626
 * C18.452.076.176.652.500 C18.452.394.750.535 C19.246.099.812
 * Diabetic ketoacidosis
 * Infuuszakjes.jpg
 * diabetic macular edema
 * class of disease
 * macular retinal edema diabetic retinopathy
 * Human disease
 * DOID:9191
 * Diabetic macular edema
 * diabetic neuropathy
 * class of disease
 * complications of diabetes mellitus peripheral neuropathy disease
 * neurological complication of persistently high blood sugar
 * DOID:9743
 * C10.668.829.300 C19.246.099.937
 * Diabetic neuropathy
 * Diapason.jpg
 * diabetic polyneuropathy
 * class of disease
 * diabetic neuropathy
 * Human disease
 * DOID:12785
 * diabetic retinopathy
 * class of disease
 * ocular manifestation of diabetes diabetic angiopathy retinal vascular disease disease
 * human disease
 * DOID:8947
 * C11.768.257 C14.907.320.382 C19.246.099.500.382
 * Diabetic retinopathy
 * Human eyesight two children and ball normal vision.jpg
 * diaphragm disease
 * class of disease
 * muscular disease respiratory disease
 * human disease
 * DOID:10481
 * Disorders of diaphragm
 * diaphragmatic eventration
 * class of disease
 * diaphragm disease
 * congenital or acquired abnormality characterized by elevation of the hemidiaphragm
 * DOID:10480
 * C06.198.257 C16.131.314.244
 * diarrhea
 * class of disease symptom or sign
 * gastrointestinal system disease clinical sign feces and droppings symptom disease
 * loose or liquid bowel movements
 * DOID:13250
 * C23.888.821.214
 * Diarrhea
 * Multiple rotavirus particles.jpg
 * diclofenac allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger diclofenac
 * DOID:0040031
 * diencephalic astrocytoma
 * class of disease
 * diencephalic neoplasm brain glioma brain astrocytoma glioma
 * Human disease
 * DOID:4855
 * diencephalic neoplasm
 * class of disease
 * supratentorial cancer
 * human disease
 * DOID:3843
 * differentiated thyroid carcinoma
 * class of disease
 * thyroid carcinoma thyroid gland adenocarcinoma
 * Differentiated thyroid carcinoma (DTC), also known as papillary or follicular thyroid carcinoma, is a slow-growing malignancy usually presenting in adults as an asymptomatic thyroid mass
 * DOID:0080525
 * differentiating neuroblastoma
 * class of disease
 * neuroblastoma
 * Human disease
 * DOID:4160
 * diffuse alopecia areata
 * class of disease
 * alopecia areata
 * alopecia areata that involves diffuse loss of hair over the whole scalp
 * DOID:0060157
 * diffuse cutaneous mastocytosis
 * class of disease
 * cutaneous mastocytosis
 * Human disease
 * DOID:3665
 * diffuse cystic renal dysplasia
 * class of disease
 * cystic kidney disease autosomal dominant disease
 * human disease
 * DOID:0111682
 * diffuse gastric cancer
 * class of disease
 * stomach cancer
 * human disease
 * DOID:0080763
 * diffuse glomerulonephritis
 * class of disease
 * glomerulonephritis
 * Human disease
 * DOID:4781
 * diffuse infiltrative lymphocytosis syndrome
 * class of disease
 * syndrome lymphocytosis AIDS related disease
 * Human disease
 * DOID:6677
 * diffuse interstitial keratitis
 * class of disease
 * interstitial keratitis
 * Human disease
 * DOID:13353
 * diffuse large B-cell lymphoma
 * class of disease
 * B-cell lymphoma aggressive B-cell non-Hodgkin lymphoma
 * type of lymphoma (cancer)
 * DOID:0050745
 * C04.557.386.480.150.585 C15.604.515.569.480.150.585 C20.683.515.761.480.150.585
 * Diffuse large B-cell lymphoma
 * Diffuse large B cell lymphoma - cytology low mag.jpg
 * diffuse lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3923
 * diffuse meningeal melanocytosis
 * class of disease
 * central nervous system melanocytic neoplasm
 * Human disease
 * DOID:6379
 * diffuse midline glioma, H3 K27M-mutant
 * class of disease
 * glioma juvenile astrocytoma
 * human disease
 * DOID:0080684
 * diffuse peritoneal leiomyomatosis
 * class of disease
 * leiomyomatosis primary peritoneal tumor leiomyoma peritoneal benign neoplasm
 * Human disease
 * DOID:5728
 * diffuse pulmonary fibrosis
 * class of disease
 * pulmonary fibrosis
 * human disease
 * DOID:5641
 * diffuse scleroderma
 * class of disease
 * systemic scleroderma
 * variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement
 * DOID:1580
 * C17.300.799.602 C17.800.784.602
 * diffuse secondary choroid atrophy
 * class of disease
 * choroidal sclerosis
 * human disease
 * DOID:981
 * diffuse uterine leiomyomatosis
 * class of disease
 * uterine fibroid uterine corpus leiomyomatosis
 * Human disease
 * DOID:5917
 * digenic disease
 * class of disease
 * polygenic disease
 * polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes
 * DOID:0080578
 * dihydropyrimidinase deficiency
 * class of disease
 * pyrimidine metabolic disorder autosomal recessive disease
 * human disease
 * DOID:0111629
 * dilated cardiomyopathy 1A
 * class of disease
 * dilated cardiomyopathy genetic disease
 * dilated cardiomyopathy that has material basis in mutation in the LMNA gene on chromosome 1q21
 * DOID:0110425
 * dilated cardiomyopathy 1B
 * class of disease
 * dilated cardiomyopathy genetic disease
 * dilated cardiomyopathy that has material basis in variation in the chromosome region 9q13
 * DOID:0110443
 * dilated cardiomyopathy 1H
 * class of disease
 * dilated cardiomyopathy genetic disease monogenic disease
 * dilated cardiomyopathy that has material basis in variation in the chromosome region 2q14-q22
 * DOID:0110429
 * dilated cardiomyopathy 1K
 * class of disease
 * dilated cardiomyopathy genetic disease monogenic disease
 * dilated cardiomyopathy that has material basis in variation in the chromosome region 6q12-q16
 * DOID:0110437
 * dilated cardiomyopathy 1KK
 * class of disease
 * dilated cardiomyopathy genetic disease autosomal dominant disease
 * dilated cardiomyopathy that has material basis in mutation in the MYPN gene on chromosome 10q21
 * DOID:0110445
 * dilated cardiomyopathy 1Q
 * class of disease
 * dilated cardiomyopathy genetic disease monogenic disease
 * A dilated cardiomyopathy that has material basis in variation in the chromosome region 7q22.3-q31.1.
 * DOID:0110442
 * dioctophymiasis
 * class of disease
 * parasitic helminthiasis infectious disease kidney disease skin disease
 * A parasitic helminthiasis infectious disease that involves parasitic infection by the nematode Dioctophyme renale in humans after eating undercooked food. The larvae are found in the subcutaneous nodules and kidneys.
 * DOID:0050260
 * diphenylmethane-4,4'-diisocyanate allergic asthma
 * class of disease
 * isocyanates allergic asthma
 * allergic asthma to isocyanates that has allergic trigger diphenylmethane-4,4-diisocyanate
 * DOID:0040042
 * diphenylmethane-4,4'-diisocyanate allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger diphenylmethane-4,4-diisocyanate
 * DOID:0040052
 * diphtheritic cystitis
 * class of disease
 * cystitis diphtheria
 * cystitis which involves inflammation and formation of a dense fibrous false membrane on the mucous membrane of the bladder
 * DOID:13306
 * diphtheritic peritonitis
 * class of disease
 * peritonitis diphtheria
 * peritonitis which involves inflammation of peritoneal cavity by Corynebacterium diphtheriae
 * DOID:13310
 * diplegia of upper limb
 * class of disease
 * neurological disorder Diplegia
 * Human disease
 * DOID:862
 * discharging ear
 * class of disease symptom or sign
 * ear disease discharge
 * human disease
 * DOID:10261
 * discoid lupus erythematosus of eyelid
 * class of disease
 * discoid lupus erythematosus noninfectious dermatoses of eyelid
 * Human disease
 * DOID:9076
 * discrete subaortic stenosis
 * class of disease
 * subvalvular aortic stenosis
 * Human disease
 * DOID:5804
 * C14.280.484.150.070.210 C14.280.955.249.070.210
 * disease
 * class of disease
 * health problem biological process
 * abnormal condition negatively affecting organisms
 * DOID:4
 * C23.550.288
 * Diseases and disorders
 * Gabriel von Max Die ekstatische Jungfrau Katharina Emmerich.jpg
 * disease of anatomical entity
 * class of disease
 * disease
 * disease that manifests in a defined anatomical structure
 * DOID:7
 * disease of cellular proliferation
 * class of disease
 * disease
 * disease characterized by abnormally rapid cell division
 * DOID:14566
 * C04.697 C23.550.727
 * dislocation of ear ossicle
 * class of disease
 * middle ear disease conductive hearing loss ear disease
 * Human disease
 * DOID:11129
 * disodium cromoglycate allergy
 * class of disease
 * drug allergy metal allergy
 * drug allergy that has allergic trigger disodium cromoglycate
 * DOID:0040073
 * displacement of cardia through esophageal hiatus
 * class of disease
 * hiatus hernia
 * Human disease
 * DOID:12641
 * disseminated chorioretinitis
 * class of disease
 * chorioretinitis
 * Human disease
 * DOID:8787
 * disseminated eosinophilic collagen disease
 * class of disease
 * collagen disease eosinophilia
 * Human disease
 * DOID:9499
 * disseminated intravascular coagulation
 * class of disease
 * thrombophilia disease
 * pathological process characterized by the widespread activation of the clotting cascade that results in the formation of blood clots in the small blood vessels throughout the body
 * DOID:11247
 * C15.378.100.220 C15.378.463.250 C15.378.925.220
 * Disseminated intravascular coagulation
 * DIC With Microangiopathic Hemolytic Anemia.jpg
 * disseminated superficial actinic porokeratosis
 * class of disease
 * keratosis porokeratosis
 * Human disease
 * DOID:3805
 * dissociated nystagmus
 * class of disease
 * pathologic nystagmus
 * Human disease
 * DOID:13174
 * dissociative amnesia
 * class of disease
 * dissociative disorder amnesia disease
 * Human disease
 * DOID:11037
 * Dissociative amnesia
 * dissociative disorder
 * class of disease
 * mental disorder dissociation disease
 * disease of mental health in which the normally well-integrated functions of memory, identity, perception, or consciousness are separated (dissociated)
 * DOID:10935
 * F03.300
 * distal arthrogryposis type 1
 * class of disease
 * distal arthrogryposis
 * human disease
 * DOID:0111596
 * distal arthrogryposis type 10
 * class of disease
 * autosomal dominant disease distal arthrogryposis
 * human disease
 * DOID:0111593
 * distal arthrogryposis type 1A
 * class of disease
 * autosomal dominant disease distal arthrogryposis type 1
 * human disease
 * DOID:0111597
 * distal arthrogryposis type 1B
 * class of disease
 * distal arthrogryposis type 1 autosomal dominant disease
 * human disease
 * DOID:0111598
 * distal arthrogryposis type 2A
 * class of disease
 * Freeman–Sheldon syndrome autosomal dominant disease
 * human disease
 * DOID:0111605
 * distal arthrogryposis type 2B1
 * class of disease
 * autosomal dominant disease Sheldon-Hall syndrome
 * human disease
 * DOID:0111600
 * distal arthrogryposis type 2B2
 * class of disease
 * Sheldon-Hall syndrome autosomal dominant disease
 * human disease
 * DOID:0111601
 * distal arthrogryposis type 2B3
 * class of disease
 * Sheldon-Hall syndrome autosomal dominant disease
 * human disease
 * DOID:0111602
 * distal arthrogryposis type 3
 * class of disease
 * autosomal dominant disease distal arthrogryposis
 * human disease
 * DOID:0111607
 * distal arthrogryposis type 4
 * class of disease
 * distal arthrogryposis
 * human disease
 * DOID:0111610
 * distal arthrogryposis type 5
 * class of disease
 * autosomal dominant disease distal arthrogryposis
 * human disease
 * DOID:0111608
 * distal arthrogryposis type 5D
 * class of disease
 * distal arthrogryposis autosomal recessive disease
 * human disease
 * DOID:0111594
 * distal arthrogryposis type 6
 * class of disease
 * distal arthrogryposis
 * human disease
 * DOID:0111609
 * distal biliary tract carcinoma
 * class of disease
 * bile duct carcinoma extrahepatic bile duct carcinoma
 * Human disease
 * DOID:5923
 * distal hereditary motor neuronopathy type 2
 * class of disease
 * autosomal dominant distal hereditary motor neuronopathy characterized by adult onset of slowly progressive distal atrophy and weakness
 * DOID:0111206
 * distal hereditary motor neuronopathy type 2A
 * class of disease
 * distal hereditary motor neuronopathy type 2
 * A distal hereditary motor neuropathy type 2 that has material basis in heterozygous mutation in HSPB8 on 12q24.23.
 * DOID:0111208
 * distal hereditary motor neuronopathy type 5
 * class of disease
 * autosomal dominant distal hereditary motor neuropathy
 * autosomal dominant distal hereditary motor neuronopathy characterized by muscle weakness and wasting, predominantly confined to the hands, and often exclusively involve thenar and/or interosseus dorsalis I eminences
 * DOID:0111203
 * distal hereditary motor neuronopathy type 5A
 * class of disease
 * distal hereditary motor neuronopathy type 5
 * A distal hereditary motor neuronopathy type 5 that has material basis in heterozygous mutation in GARS on 7p14.3 or BSCL2 on 11q12.3.
 * DOID:0111204
 * distal hereditary motor neuronopathy type 7
 * class of disease
 * autosomal dominant distal hereditary motor neuropathy
 * autosomal dominant distal hereditary motor neuronopathy characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis
 * DOID:0111199
 * distal hereditary motor neuronopathy type 7A
 * class of disease
 * distal hereditary motor neuronopathy type 7
 * human disease
 * DOID:0111201
 * distal hereditary motor neuronopathy type 7B
 * class of disease
 * distal hereditary motor neuronopathy type 7
 * A distal hereditary motor neuropathy type 7 that has material basis in heterozygous mutation in DCTN1 on 2p13.1.
 * DOID:0111202
 * distal hereditary motor neuronopathy type 8
 * class of disease
 * autosomal dominant distal hereditary motor neuropathy
 * human disease
 * DOID:0111215
 * distal hereditary motor neuronopathy type 9
 * class of disease
 * autosomal dominant distal hereditary motor neuropathy
 * human disease
 * DOID:0111212
 * distal hereditary motor neuropathy type 1
 * class of disease
 * nervous system heredodegenerative disease autosomal dominant distal hereditary motor neuropathy
 * autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration
 * DOID:0111200
 * distal hereditary motor neuropathy type 2B
 * class of disease
 * distal hereditary motor neuronopathy type 2
 * A distal hereditary motor neuropathy type 2 that has material basis in heterozygous mutation in HSPB1 on 7q11.23.
 * DOID:0111207
 * distal muscular dystrophy 3
 * class of disease
 * distal muscular dystrophy that has significant linkage to 2 distinct regions on chromosomes 8p22-q11 and 12q13-q22
 * DOID:0111189
 * distal myopathy 1
 * class of disease
 * distal muscular dystrophy genetic disease autosomal dominant disease
 * distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11
 * DOID:0070197
 * distal spinal muscular atrophy type 3
 * class of disease
 * nervous system heredodegenerative disease autosomal recessive distal hereditary motor neuropathy autosomal recessive distal hereditary motor neuronopathy
 * human disease
 * DOID:0111211
 * distal spinal muscular atrophy type 4
 * class of disease
 * autosomal recessive distal hereditary motor neuronopathy
 * human disease
 * DOID:0111213
 * distal spinal muscular atrophy type 5
 * class of disease
 * autosomal recessive distal hereditary motor neuronopathy
 * human disease
 * DOID:0111214
 * disuse amblyopia
 * class of disease
 * amblyopia
 * Human disease
 * DOID:10378
 * diversion colitis
 * class of disease
 * colitis
 * colitis caused by diversion of the fecal stream due to complication of ileostomy or colostomy
 * DOID:0060187
 * diverticulitis
 * class of disease symptom or sign
 * intestinal disease diverticular disease inflammatory disease sigmoiditis disease
 * digestive disease caused by an inflammation of a herniating pouch (diverticulum) within the wall of the intestine, most often colon
 * DOID:7475
 * C01.539.463.199.375 C06.405.205.282.500
 * Diverticulitis
 * Diverticula, sigmoid colon.jpg
 * diverticulitis of colon
 * class of disease
 * colonic disease diverticulitis colonic diverticulosis
 * colonic disease characterized by the formation and inflammation of diverticula within the colon wall
 * DOID:13254
 * C06.405.469.158.587.500 C01.539.463.199.375.250 C06.405.205.282.500.250
 * dominant beta-thalassemia
 * class of disease
 * beta thalassemia autosomal dominant disease
 * Dominant beta-thalassemia is a form of beta-thalassemia (see this term) resulting in moderate to severe anemia
 * DOID:0080770
 * dominant dystrophic epidermolysis bullosa
 * class of disease
 * epidermolysis bullosa dystrophica autosomal dominant disease
 * human disease
 * DOID:0080224
 * dominant pericentral pigmentary retinopathy
 * class of disease
 * retinitis pigmentosa autosomal dominant disease
 * retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life
 * DOID:0110420
 * dopamine beta-hydroxylase deficiency
 * class of disease
 * autonomic nervous system disease Congenital disorders of amino acid metabolism inherited metabolic disorder primary orthostatic hypotension disorder of catecholamine synthesis neurometabolic disease ptosis neurological disorder genetic disease
 * genetic metabolic disorder
 * DOID:0090145
 * double pterygium
 * class of disease
 * pterygium
 * Human disease
 * DOID:10525
 * drug allergy
 * class of disease
 * allergy drug intolerance
 * human disease
 * DOID:0060500
 * C20.543.206 C25.100.468
 * drug psychosis
 * class of disease
 * drug-induced mental disorder substance-induced psychosis psychosis
 * Psychotic organic mental disorders resulting from the toxic effect of drugs and chemicals or other harmful substance
 * DOID:1742
 * C25.723.809 C25.775.746 F03.700.675.600 F03.900.746
 * drug-induced hearing loss
 * class of disease
 * deafness
 * nonsyndromic deafness that is characterized by cochlear or vestibular dysfunction resulting in loss of hearing caused by drug ototoxicity
 * DOID:0070310
 * drug-induced hepatitis
 * class of disease
 * hepatitis hepatotoxicity disease
 * Human disease
 * DOID:2044
 * C06.552.195.200 C25.100.562.200 C25.723.260.200
 * drug-induced lupus erythematosus
 * class of disease symptom or sign
 * adverse drug reaction lupus erythematosus disease
 * lupus erythematosus caused by chronic use of certain drugs
 * DOID:0040093
 * Procainamide.svg
 * drug-induced mental disorder
 * class of disease
 * substance-related disorder adverse drug reaction substance-induced psychosis
 * Human disease
 * DOID:1203
 * dry beriberi
 * class of disease
 * beriberi
 * beriberi that is located in the nervous system and has symptom difficulty walking, numbness in extremities, tingling in extremities, paralysis of lower legs, difficulty speaking, confusion, and vomiting
 * DOID:0070318
 * dry eye syndrome
 * class of disease
 * lacrimal apparatus disease
 * corneal and conjunctival dryness due to deficient tear production
 * DOID:10140
 * C11.496.260
 * dumping syndrome
 * class of disease
 * postgastrectomy syndrome disease
 * Human disease
 * DOID:14495
 * C06.405.748.630.310 C23.550.767.812.500
 * duodenal atresia
 * class of disease
 * atresia duodenal stenosis atresia of small intestine gastroduodenal malformation intestinal atresia disease
 * congenital disorder of digestive system
 * DOID:0080216
 * Duodenal atresia
 * duodenal disease
 * class of disease
 * intestinal disease small-intestine disease
 * Human disease
 * DOID:4072
 * C06.405.469.275
 * duodenal gastrinoma
 * class of disease
 * duodenum cancer gastrinoma duodenal neuroendocrine tumor, well differentiated, low or intermediate grade
 * Human disease
 * DOID:7959
 * duodenal neoplasm
 * class of disease
 * small intestine neoplasm duodenal disease
 * Human disease
 * DOID:1737
 * C04.588.274.476.411.445 C06.301.371.411.445 C06.405.249.411.445 C06.405.469.275.270 C06.405.469.491.445
 * Duodenal neoplasms
 * duodenal obstruction
 * class of disease
 * duodenal disease bowel obstruction
 * Human disease
 * DOID:3558
 * C06.405.469.275.395 C06.405.469.531.311
 * duodenal somatostatinoma
 * class of disease
 * duodenum cancer duodenal neuroendocrine tumor, well differentiated, low or intermediate grade
 * Human disease
 * DOID:7479
 * duodenal ulcer
 * class of disease
 * peptic ulcer disease
 * Human disease
 * DOID:1724
 * C06.405.469.275.800.348 C06.405.748.586.349
 * Duodenal ulcers
 * duodenitis
 * class of disease
 * intestinal disease disease
 * Human disease
 * DOID:8643
 * C06.405.205.462.249 C06.405.469.275.600 C06.405.469.326.750
 * Duodenitis
 * duodenum adenocarcinoma
 * class of disease
 * duodenum cancer small intestine adenocarcinoma adenocarcinoma
 * duodenum cancer that derives from epithelial cells of glandular origin
 * DOID:10816
 * Duodenal adenocarcinoma
 * duodenum adenoma
 * class of disease
 * duodenal neoplasm adenoma of small intestine duodenal disease benign neoplasms by histologic type adenoma
 * duodenal benign neoplasm that has material basis in epithelial tissue with glandular origin
 * DOID:0050927
 * duodenum cancer
 * class of disease
 * small intestine cancer small intestine carcinoma duodenal disease duodenal neoplasm
 * small intestine cancer that is located in the beginning section of the small intestine
 * DOID:10021
 * Duodenal cancer
 * Duodenal adenocarcinoma.png
 * dysembryoplastic neuroepithelial tumour
 * class of disease
 * neuronal and mixed glio-neuronal tumor low grade glioma central nervous system organ benign neoplasm epilepsy
 * type of brain tumour
 * DOID:2679
 * Dysembryoplastic neuroepithelial tumour
 * DNET HE.jpg
 * dysgammaglobulinemia
 * class of disease
 * selective immunoglobulin deficiency disease
 * selective immunoglobulin deficiency disease that is caused by a reduction in some types of gamma globulins
 * DOID:11702
 * C15.378.147.333 C20.673.430
 * dysgerminoma
 * class of disease
 * germ cell cancer ovarian cancer disease
 * germ cell cancer that derives from cells that give rise to egg cells
 * DOID:4441
 * C04.557.465.330.300
 * Dysgerminoma
 * Dysgerminoma, high mag.jpg
 * dysgerminoma of ovary
 * class of disease
 * dysgerminoma ovarian primitive germ cell tumor
 * dysgerminoma that is located in the ovary
 * DOID:5511
 * Ovarian dysgerminoma
 * dysgraphia
 * class of disease
 * writing disorder learning disability disease
 * developmental or acquired neurological condition
 * DOID:4540
 * Dysgraphia
 * Dysgraphia1.jpg
 * dyshormonogenic goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:12175
 * dyskinesia of esophagus
 * class of disease
 * esophageal motility disorder esophageal disease
 * human disease
 * DOID:9192
 * dyskinetic cerebral palsy
 * class of disease
 * cerebral palsy
 * human disease
 * DOID:0050672
 * dysplastic nevus syndrome
 * class of disease
 * autosomal dominant disease syndrome disease
 * Human skin disease
 * DOID:10041
 * C04.557.665.560.260 C04.700.305 C16.320.700.305
 * Dysplastic nevus syndrome
 * dysthymic disorder
 * class of disease
 * mood disorder disease
 * psychological disorder
 * DOID:12139
 * F03.600.300.400
 * dystonia
 * class of disease
 * movement disorders rare genetic dystonia disease
 * human disease
 * DOID:543
 * C10.597.350.300 C23.888.592.350.300
 * Dystonia
 * Dystonia2010.JPG
 * dystonia 21
 * class of disease
 * dystonia generalized isolated dystonia genetic disease autosomal dominant disease
 * A dystonia characterized by autosomal dominant inheritance of late onset pure torsion dystonia that has material basis in variation in the chromosome region 2q14.3-q21.3.
 * DOID:0090046
 * dystonia 5
 * class of disease
 * dystonia genetic disease autosomal dominant disease autosomal recessive disease
 * human disease
 * DOID:0090043
 * dystransthyretinemic hyperthyroxinemia
 * class of disease
 * hyperthyroxinemia autosomal dominant disease
 * human disease
 * DOID:0080219
 * dystrophies primarily involving the retinal pigment epithelium
 * class of disease
 * fundus dystrophy retinitis pigmentosa
 * Human disease
 * DOID:14252
 * ear disease
 * class of disease
 * sensory system disease
 * human disease
 * DOID:2742
 * C09.218
 * Diseases and disorders of the ear and mastoid process
 * early congenital syphilis
 * class of disease
 * congenital syphilis
 * Human disease
 * DOID:0050488
 * early infantile epileptic encephalopathy 1
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy characterized by X-linked recessive inheritance that has material basis in mutation in the ARX gene on chromosome Xp21
 * DOID:0080468
 * early infantile epileptic encephalopathy 12
 * class of disease
 * Ohtahara syndrome
 * An early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the PLCB1 gene on chromosome 20p12.3.
 * DOID:0080459
 * early infantile epileptic encephalopathy 13
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SCN8A gene on chromosome 12q13
 * DOID:0080445
 * early infantile epileptic encephalopathy 14
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy characterized by refractory focal seizures developing by 6 months of age and arrest of psychomotor development that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34
 * DOID:0080439
 * early infantile epileptic encephalopathy 16
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080449
 * early infantile epileptic encephalopathy 19
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRA1 gene on chromosome 5q34
 * DOID:0080431
 * early infantile epileptic encephalopathy 2
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080467
 * early infantile epileptic encephalopathy 21
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the NECAP1 gene on chromosome 12p13
 * DOID:0080443
 * early infantile epileptic encephalopathy 23
 * class of disease
 * Ohtahara syndrome autosomal recessive disease
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the DOCK7 gene on chromosome 1p31
 * DOID:0080415
 * early infantile epileptic encephalopathy 24
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the HCN1 gene on chromosome 5p12
 * DOID:0080429
 * early infantile epileptic encephalopathy 25
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13
 * DOID:0080453
 * early infantile epileptic encephalopathy 26
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the KCNB1 gene on chromosome 20q13
 * DOID:0080461
 * early infantile epileptic encephalopathy 27
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080444
 * early infantile epileptic encephalopathy 29
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the AARS gene on chromosome 16q22
 * DOID:0080451
 * early infantile epileptic encephalopathy 30
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SIK1 gene on chromosome 21q22
 * DOID:0080465
 * early infantile epileptic encephalopathy 31
 * class of disease
 * Ohtahara syndrome developmental and epileptic encephalopathy
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the DNM1 gene on chromosome 9q34
 * DOID:0080437
 * early infantile epileptic encephalopathy 32
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080416
 * early infantile epileptic encephalopathy 33
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the EEF1A2 gene on chromosome 20q13
 * DOID:0080463
 * early infantile epileptic encephalopathy 34
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080460
 * early infantile epileptic encephalopathy 35
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080458
 * early infantile epileptic encephalopathy 37
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080435
 * early infantile epileptic encephalopathy 38
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous mutation in the ARV1 gene on chromosome 1q42
 * DOID:0080417
 * early infantile epileptic encephalopathy 39
 * class of disease
 * Ohtahara syndrome
 * infantile epileptic encephalopathy that has material basis in mutation in the SLC25A12 gene on chromosome 2q31
 * DOID:0080349 DOID:0080423
 * early infantile epileptic encephalopathy 40
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the GUF1 gene on chromosome 4p12
 * DOID:0080427
 * early infantile epileptic encephalopathy 41
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SLC1A2 gene on chromosome 11p13
 * DOID:0080442
 * early infantile epileptic encephalopathy 42
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the CACNA1A gene on chromosome 19p13
 * DOID:0080454
 * early infantile epileptic encephalopathy 43
 * class of disease
 * Ohtahara syndrome autosomal dominant disease
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRB3 gene on chromosome 15q11
 * DOID:0080447
 * early infantile epileptic encephalopathy 44
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22
 * DOID:0080424
 * early infantile epileptic encephalopathy 45
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRB1 gene on chromosome 4p13
 * DOID:0080428
 * early infantile epileptic encephalopathy 46
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GRIN2D gene on chromosome 19q13
 * DOID:0080456
 * early infantile epileptic encephalopathy 47
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the FGF12 gene on chromosome 3q28
 * DOID:0080425
 * early infantile epileptic encephalopathy 48
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080448
 * early infantile epileptic encephalopathy 49
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080441
 * early infantile epileptic encephalopathy 51
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy characterized by onset of intractable seizures and hypotonia in the first days or weeks of life that has material basis in homozygous or compound heterozygous mutation in the MDH2 gene on chromosome 7q11
 * DOID:0080433
 * early infantile epileptic encephalopathy 52
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080455
 * early infantile epileptic encephalopathy 53
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080464
 * early infantile epileptic encephalopathy 54
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080418
 * early infantile epileptic encephalopathy 55
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080283
 * early infantile epileptic encephalopathy 56
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080282
 * early infantile epileptic encephalopathy 57
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080284
 * early infantile epileptic encephalopathy 58
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080285
 * early infantile epileptic encephalopathy 59
 * class of disease
 * Ohtahara syndrome infantile epileptic encephalopathy autosomal dominant disease
 * human disease
 * DOID:0080291
 * early infantile epileptic encephalopathy 60
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the CNPY3 gene on chromosome 6p
 * DOID:0080432
 * early infantile epileptic encephalopathy 61
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the ADAM22 gene on chromosome 7q21
 * DOID:0080434
 * early infantile epileptic encephalopathy 62
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SCN3A gene on chromosome 2q24
 * DOID:0080420
 * early infantile epileptic encephalopathy 63
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the CPLX1 gene on chromosome 4p16
 * DOID:0080426
 * early infantile epileptic encephalopathy 65
 * class of disease
 * Ohtahara syndrome
 * human disease
 * DOID:0080430
 * early infantile epileptic encephalopathy 66
 * class of disease
 * Ohtahara syndrome
 * early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the PACS2 gene on chromosome 14q32
 * DOID:0080446
 * early infantile epileptic encephalopathy 8
 * class of disease
 * Ohtahara syndrome hyperekplexia
 * human disease
 * DOID:0080215
 * early infantile epileptic encephalopathy 82
 * class of disease
 * autosomal recessive disease Ohtahara syndrome
 * human disease
 * DOID:0080715
 * early invasive cervical adenocarcinoma
 * class of disease
 * cervical adenocarcinoma
 * Human disease
 * DOID:8307
 * early onset absence epilepsy
 * class of disease
 * childhood electroclinical syndrome
 * childhood electroclinical syndrome characterized by the occurrence of typical absence seizures starting between the age of four and ten years
 * DOID:0050708
 * early yaws
 * class of disease
 * yaws
 * A yaws that results in initial papule at the site of entry of bacteria. Without treatment, this is followed by disseminated skin lesions over the body. Bone pain and bone lesions may also occur.
 * DOID:10568
 * early-onset vitamin B6-dependent epilepsy
 * class of disease
 * autosomal recessive disease epilepsy
 * human disease
 * DOID:0080769
 * eating disorder
 * class of disease
 * specific developmental disorder nutrition disorder disease
 * habit of eating either insufficient or excessive food, to the detriment of health
 * DOID:8670
 * F03.400
 * Eating disorder
 * eccrine acrospiroma
 * class of disease
 * eccrine sweat gland neoplasm
 * Human disease
 * DOID:5442
 * C04.557.470.035.175.588 C04.557.470.550.175.588
 * eccrine adenocarcinoma
 * class of disease
 * eccrine sweat gland cancer adenocarcinoma
 * eccrine sweat gland cancer that derives from epithelial cells of glandular origin
 * DOID:4920
 * eccrine mixed tumor of skin
 * class of disease
 * eccrine sweat gland neoplasm
 * Human disease
 * DOID:2079
 * Chondroid syringoma
 * eccrine papillary adenocarcinoma
 * class of disease
 * eccrine adenocarcinoma
 * Human disease
 * DOID:5591
 * eccrine sweat gland cancer
 * class of disease
 * sweat gland cancer eccrine sweat gland neoplasm
 * Human disease
 * DOID:4921
 * eccrine sweat gland neoplasm
 * class of disease
 * sweat gland neoplasm
 * human disease
 * DOID:173
 * eclampsia
 * class of disease
 * pre-eclampsia disease life emergency
 * pre-eclampsia characterized by the presence of seizures
 * DOID:13593 DOID:12269 DOID:12268
 * C13.703.395.124
 * Eclampsia
 * Dissection of uterus at term eclampsia.jpg
 * ecthyma
 * class of disease
 * impetigo
 * Human disease
 * DOID:11907
 * C01.150.252.410.890.168 C01.150.252.819.210 C01.800.720.210 C17.800.695.210 C17.800.838.765.210
 * Ecthyma
 * ectodermal dysplasia 1
 * class of disease
 * hypohidrotic ectodermal dysplasia X-linked recessive disease
 * human disease
 * DOID:0111664
 * ectodermal dysplasia 10A
 * class of disease
 * hypohidrotic ectodermal dysplasia autosomal dominant disease
 * human disease
 * DOID:0111663
 * ectodermal dysplasia 10B
 * class of disease
 * hypohidrotic ectodermal dysplasia autosomal recessive disease
 * human disease
 * DOID:0111665
 * ectodermal dysplasia 11B
 * class of disease
 * hypohidrotic ectodermal dysplasia autosomal recessive disease
 * human disease
 * DOID:0111654
 * ectodermal dysplasia 14
 * class of disease
 * autosomal recessive disease ectodermal dysplasia
 * human disease
 * DOID:0111662
 * ectodermal dysplasia 15
 * class of disease
 * ectodermal dysplasia autosomal recessive disease
 * human disease
 * DOID:0111651
 * ectodermal dysplasia 4
 * class of disease
 * autosomal recessive disease pure hair-nail type ectodermal dysplasia
 * human disease
 * DOID:0111658
 * ectodermal dysplasia 5
 * class of disease
 * pure hair-nail type ectodermal dysplasia autosomal recessive disease
 * human disease
 * DOID:0111657
 * ectodermal dysplasia 6
 * class of disease
 * autosomal recessive disease pure hair-nail type ectodermal dysplasia
 * human disease
 * DOID:0111659
 * ectodermal dysplasia 7
 * class of disease
 * autosomal recessive disease pure hair-nail type ectodermal dysplasia
 * human disease
 * DOID:0111660
 * ectodermal dysplasia 8
 * class of disease
 * autosomal recessive disease ectodermal dysplasia
 * human disease
 * DOID:0111661
 * ectodermal dysplasia 9
 * class of disease
 * autosomal recessive disease pure hair-nail type ectodermal dysplasia
 * human disease
 * DOID:0111656
 * ectomesenchymoma
 * class of disease
 * central nervous system mesenchymal non-meningothelial tumor nervous system cancer
 * human disease
 * DOID:4055
 * ectopic Cushing syndrome
 * class of disease
 * hyperaldosteronism ACTH-dependent Cushing syndrome
 * human disease
 * DOID:0060890
 * C04.730.713.317
 * ectopic pregnancy
 * class of disease
 * female reproductive system disease human pregnancy disease
 * female reproductive system disease characterized by the implantation of the embryo outside the uterine cavity
 * DOID:0060329
 * C13.703.733
 * Ectopic pregnancy
 * Tubal Pregnancy with embryo.jpg
 * ectopic thymus
 * class of disease
 * thymus gland disease
 * Human disease
 * DOID:6307
 * ectothrix infectious disease
 * class of disease
 * tinea capitis vale hair diseases
 * Human disease
 * DOID:0050097
 * ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
 * class of disease
 * ectrodactyly–ectodermal dysplasia–cleft syndrome
 * An EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3.
 * DOID:0060784
 * ectrodactyly–ectodermal dysplasia–cleft syndrome
 * class of disease
 * autosomal dominant disease ectodermal dysplasia syndrome
 * autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate)
 * DOID:0060782
 * ectropion
 * class of disease
 * eyelid disease
 * human disease
 * DOID:1570
 * C11.338.362
 * Ectropion
 * Ectropion.JPG
 * eczematous dermatitis of eyelid
 * class of disease
 * noninfectious dermatoses of eyelid
 * Human disease
 * DOID:1893
 * egg allergy
 * class of disease
 * food allergy health effects of eggs
 * food allergy that is an allergy or hypersensitivity to dietary substances from the yolk or whites of eggs, causing an overreaction of the immune system which may lead to severe physical symptoms
 * DOID:4377
 * C20.543.480.370.150
 * Fried egg, sunny side up.jpg
 * ego-dystonic sexual orientation
 * class of disease
 * gender dysphoria disease
 * psychiatric diagnosis
 * DOID:13352
 * electroclinical syndrome
 * class of disease
 * epilepsy
 * Human disease
 * DOID:0050701
 * elephantiasis
 * class of disease
 * lymphedema
 * Human disease
 * DOID:4976
 * C15.604.496.320
 * Elephantiasis
 * embryoma
 * class of disease
 * embryonal cancer
 * carcinosarcoma and embryonal cancer that is located in embryonic tissue and results in a mass of rapidly growing cells
 * DOID:4766
 * Embryonal tumors
 * embryonal cancer
 * class of disease
 * germ cell cancer
 * germ cell cancer that is associated with an embryo
 * DOID:688
 * embryonal carcinoma
 * class of disease
 * embryonal cancer extragonadal germ cell cancer extragonadal non-dysgerminomatous germ cell tumor carcinoma disease
 * embryonal cancer that is a type of germ cell tumour, located in the ovaries or testes
 * DOID:3308
 * C04.557.465.200
 * Embryonal carcinoma
 * embryonal extrahepatic bile duct rhabdomyosarcoma
 * class of disease
 * bile duct rhabdomyosarcoma
 * Human disease
 * DOID:3253
 * embryonal rhabdomyosarcoma
 * class of disease
 * rhabdomyosarcoma embryonal cancer
 * rhabdomyosarcoma with mesenchymally-derived malignant cells resembling the developing skeletal muscle of the embryo
 * DOID:3246
 * C04.557.450.590.550.660.675 C04.557.450.795.550.660.675
 * embryonal testis carcinoma
 * class of disease
 * embryonal carcinoma testicular cancer testicular non-seminomatous germ cell cancer testicular pure germ cell tumor
 * embryonal carcinoma that is located in the testis
 * DOID:5680
 * emphysematous cholecystitis
 * class of disease
 * cystitis cholecystitis
 * bacterial infectious disease with inflammation of the gallbladder characterized by air-filled expansions in interstitial or subcutaneous tissues
 * DOID:9765
 * C06.130.564.263.500.500
 * enamel caries
 * class of disease
 * dental caries
 * Human disease
 * DOID:217
 * enamel erosion
 * class of disease
 * dental erosion
 * Human disease
 * DOID:2497
 * encapsulated thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:3278
 * Encapsulated thymoma.jpg
 * encephalitis
 * class of disease symptom or sign
 * brain inflammatory disease encephalopathy neurological symptom disease
 * acute inflammation of the brain with flu-like symptoms
 * DOID:9588
 * C10.228.140.430 C10.586.250
 * Encephalitis
 * Hsv encephalitis.jpg
 * encephalomalacia
 * class of disease
 * encephalopathy
 * Human disease
 * DOID:2034
 * C10.228.140.461
 * encephalomyelitis
 * class of disease
 * central nervous system disease inflammatory disease disease
 * inflammation of the brain and spinal cord
 * DOID:640
 * C10.228.228.291 C10.228.440 C01.207.291
 * Encephalomyelitis
 * encephalopathy
 * class of disease
 * central nervous system disease disease
 * central nervous system diseases located in the brain
 * DOID:936
 * C10.228.140
 * Encephalopathy
 * encephalopathy due to defective mitochondrial and peroxisomal fission 1
 * class of disease
 * syndrome
 * human disease
 * DOID:0070347
 * end stage renal failure
 * class of disease
 * chronic renal insufficiency
 * human disease
 * DOID:783
 * endemic goiter
 * class of disease
 * goiter nutritional deficiency disease
 * human disease
 * DOID:13198
 * C19.874.283.300
 * endobronchial leiomyoma
 * class of disease
 * lung leiomyoma bronchial neoplasm
 * Human disease
 * DOID:6608
 * endobronchial lipoma
 * class of disease
 * bronchial neoplasm respiratory system benign neoplasm lipoma
 * Human disease
 * DOID:10183
 * endocardial fibroelastosis
 * class of disease
 * endocardium disease familial restrictive cardiomyopathy non-familial restrictive cardiomyopathy non-familial dilated cardiomyopathy
 * endocardium disease that is characterized by endocardium becoming massively fibrosed and thickened wih elastic tissue resulting in a restrictive cardiomyopathy.
 * DOID:12929
 * C14.280.238.281
 * endocarditis
 * class of disease symptom or sign
 * endocardium disease pancarditis cardiovascular system symptom disease
 * endocardium disease characterized by inflammation of the endocardium of the heart chambers and valves
 * DOID:10314
 * C14.280.282
 * Endocarditis
 * Blood culture negative endocarditis.jpg
 * endocardium cancer
 * class of disease
 * heart cancer neoplasm of endocardium endocardium disease
 * Human disease
 * DOID:5877
 * endocervical adenocarcinoma
 * class of disease
 * endocervical carcinoma adenocarcinoma
 * endocervical carcinoma that derives from epithelial cells of glandular origin
 * DOID:0050940
 * Endocervical adenocarcinoma
 * endocervical carcinoma
 * class of disease
 * cervix carcinoma malignant neoplasm of endocervix
 * Human disease
 * DOID:7519
 * endocervical type cervical adenomyoma
 * class of disease
 * cervical adenomyoma
 * Human disease
 * DOID:8177
 * endocervical type cervical mucinous adenocarcinoma
 * class of disease
 * cervical mucinous adenocarcinoma
 * Human disease
 * DOID:8340
 * endocervicitis
 * class of disease
 * cervicitis inflammatory disease
 * Human disease
 * DOID:5757
 * endocrine exophthalmos
 * class of disease
 * orbital disease exophthalmos
 * Human disease
 * DOID:12359
 * endocrine gland cancer
 * class of disease
 * organ system cancer endocrine gland neoplasm endocrine system disease
 * organ system cancer located in endocrine system that is characterized by uncontrolled cellular proliferation of the hormone producing glands of the endocrine system
 * DOID:170
 * endocrine organ benign neoplasm
 * class of disease
 * organ system benign neoplasm endocrine gland neoplasm endocrine system disease
 * organ system benign neoplasm that is located in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body
 * DOID:0060089
 * endocrine pancreas disease
 * class of disease
 * pancreas disease endocrine system disease
 * disease involving the endocrine pancreas
 * DOID:1428
 * endocrine system disease
 * class of disease
 * disease of anatomical entity disease
 * type of disease affecting the endocrine system
 * DOID:28 DOID:1922
 * C19
 * Endocrine diseases and disorders
 * Illu endocrine system.png
 * endodermal sinus pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:7302
 * endogenous depression
 * class of disease
 * major depressive disorder endogenous mental disorder
 * mental depression that is characterized by a dysregulation of the endogenous opioid system and not of the monaminergic system
 * DOID:1595
 * endometrial adenocarcinoma
 * class of disease
 * endometrial carcinoma adenocarcinoma
 * endometrial carcinoma that derives from epithelial cells of glandular origin
 * DOID:2870
 * Endometrial adenocarcinoma
 * endometrial adenosquamous carcinoma
 * class of disease
 * adenosquamous carcinoma endometrial squamous cell carcinoma squamous cell carcinoma endometrial cancer
 * endometrial carcinoma that derives from squamous cells and gland-like cells
 * DOID:5631
 * endometrial cancer
 * class of disease
 * uterine cancer uterine corpus cancer endometriosis endometrial neoplasm disease
 * uterine cancer that is located in tissues lining the uterus
 * DOID:1380
 * Endometrial cancer
 * Endometrioid endometrial adenocarcinoma low mag.jpg
 * endometrial carcinoma
 * class of disease
 * endometrial cancer carcinoma
 * endometrial cancer that is located in the tissue lining the uterus
 * DOID:2871
 * C04.557.470.200.025.240 C04.588.945.418.948.585.124 C13.351.500.056.630.705.331 C13.351.937.418.685.331 C13.351.937.418.875.200.124 C19.391.630.705.331
 * endometrial clear cell adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5299
 * endometrial disease
 * class of disease
 * uterine disease
 * Human disease
 * DOID:1005
 * Diseases and disorders of endometrium
 * endometrial hyperplasia
 * class of disease
 * uterine benign neoplasm endometrial disease disease
 * uterine benign neoplasm that is characterized by excessive proliferation of the cells of the endometrium
 * DOID:0080365
 * C13.351.500.852.228
 * endometrial mixed adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:7664
 * endometrial mucinous adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma mucinous adenocarcinoma
 * human disease
 * DOID:3707
 * endometrial small cell carcinoma
 * class of disease
 * uterine cancer endometrial cancer carcinoma
 * Human disease
 * DOID:7139
 * endometrial squamous cell carcinoma
 * class of disease
 * endometrial carcinoma squamous cell carcinoma
 * Human disease
 * DOID:5533
 * endometrial stromal nodule
 * class of disease
 * uterine benign neoplasm endometrial stromal tumour
 * human disease
 * DOID:1373
 * EndometrialStromalNodule.JPG
 * endometrial stromal sarcoma
 * class of disease
 * endometrial stromal tumour
 * human disease
 * DOID:4226
 * C04.557.435.775 C04.557.450.795.332.500 C13.351.500.852.762.200.500.500 C13.351.937.418.875.200.374.500
 * Endometrial stromal sarcoma
 * endometrial stromal tumour
 * class of disease
 * endometrial cancer
 * human disease
 * DOID:5166
 * C04.557.450.565.325 C04.557.450.795.332 C13.351.500.852.762.200.500 C13.351.937.418.875.200.374
 * endometrial transitional cell carcinoma
 * class of disease
 * endometrial carcinoma transitional cell carcinoma
 * Human disease
 * DOID:4005
 * endometrial type cervical adenomyoma
 * class of disease
 * cervical adenomyoma
 * Human disease
 * DOID:8178
 * endometrioid ovary carcinoma
 * class of disease
 * ovary adenocarcinoma endometrial adenocarcinoma uterine cancer endometrial carcinoma ovarian endometrial cancer
 * Human disease
 * DOID:5828
 * endometriosis
 * class of disease
 * female reproductive system disease endometrial disease disease
 * disease linked to the female reproductive system
 * DOID:289
 * C12.050.351.500.163 C12.100.250.163
 * Endometriosis
 * Endometriosis.jpg
 * endometriosis of intestine
 * class of disease
 * endometriosis intestinal disease
 * Human disease
 * DOID:11428
 * Endometriosis of intestine
 * endometriosis of ovary
 * class of disease
 * endometriosis ovarian disease
 * Human disease
 * DOID:11432
 * endometriosis of pelvic peritoneum
 * class of disease
 * endometriosis
 * Human disease
 * DOID:11429
 * endometriosis of rectovaginal septum and vagina
 * class of disease
 * endometriosis vaginal disease
 * Human disease
 * DOID:11431
 * endometritis
 * class of disease
 * endometrial disease disease
 * inflammation of inner lining of uterus
 * DOID:1002
 * C13.351.500.056.750.249 C13.351.500.852.299
 * Endometritis
 * Endometritis - 2 - cropped - very high mag.jpg
 * endometrium carcinoma in situ
 * class of disease
 * in situ carcinoma endometriosis uterus carcinoma in situ
 * Human disease
 * DOID:5172
 * endomyocardial fibrosis
 * class of disease
 * restrictive cardiomyopathy
 * Human disease
 * DOID:12932
 * C14.280.238.406
 * endophthalmitis
 * class of disease
 * globe disease eye inflammation disease
 * globe disease that is characterized by inflammation of the inside of the eye
 * DOID:4692
 * C01.375.265 C11.294.265
 * endosalpingiosis
 * class of disease
 * endometriosis
 * Human disease
 * DOID:11427
 * Endosalpingiosis
 * endothrix infectious disease
 * class of disease
 * tinea capitis vale hair diseases
 * tinea capitis that results in fungal infection located in hair, has material basis in Ascomycota fungi that belong to a group called dermatophytes, which produce arthroconidia within the hair shaft only
 * DOID:0050105
 * enhanced S-cone syndrome
 * class of disease
 * retinal disease vitreoretinal degeneration unclassified primitive or secondary maculopathy genetic disease autosomal recessive disease
 * Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis)
 * DOID:0090059
 * enophthalmos
 * class of disease
 * orbital disease enophthalmia disease
 * posterior displacement of the eyeball within the orbit due to changes in the volume of the orbit (bone) relative to its contents
 * DOID:11175
 * C11.675.319
 * enteric pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8362
 * enterocele
 * class of disease
 * pelvic organ prolapse
 * Human disease
 * DOID:1283
 * Enterocele
 * enthesopathy
 * class of disease
 * connective tissue disease disease
 * human disease: a disorder involving the attachment of a tendon or ligament to a bone
 * DOID:204
 * C05.651.869.653 C26.874.800.750
 * Enthesopathy
 * EnthesopathyPelvisCT.png
 * entropion
 * class of disease
 * eyelid disease disease
 * medical condition in which the eyelid (usually the lower lid) folds inward
 * DOID:12397
 * C11.338.443
 * Entropion
 * Canine entropion.JPG
 * environmental induced asthma
 * class of disease
 * intrinsic asthma
 * human disease
 * DOID:0080819
 * eosinophilia-myalgia syndrome
 * class of disease
 * eosinophilia
 * Human disease
 * DOID:998
 * C05.651.290 C10.668.491.387 C15.378.553.231.335
 * Eosinophilia–myalgia syndrome
 * eosinophilic gastritis
 * class of disease
 * gastritis chronic gastritis
 * Human disease
 * DOID:4030
 * eosinophilic meningitis
 * class of disease
 * chronic meningitis
 * Human disease
 * DOID:10361
 * eosinophilic pneumonia
 * class of disease
 * pneumonia eosinophilia disease
 * disease in which an eosinophil, a type of white blood cell, accumulates in the lung
 * DOID:9498 DOID:5870
 * C08.381.750 C15.378.553.231.549.750
 * eosinophilic variant of chromophobe renal cell carcinoma
 * class of disease
 * chromophobe renal cell carcinoma
 * Human disease
 * DOID:6606
 * ependymal tumor
 * class of disease
 * ependymal tumor cerebral ventricle cancer carcinoma
 * malignant glioma that is derived from ependymal cells, a type of glial cell, located in ventricle lining within the central part of the brain
 * DOID:5074
 * Ependymal tumors
 * epicardium cancer
 * class of disease
 * pericardium cancer neoplasm of epicardium
 * Human disease
 * DOID:4699
 * epicardium lipoma
 * class of disease
 * heart lipoma lipoma benign neoplasm of epicardium
 * Human disease
 * DOID:6284
 * epidermal appendage tumor
 * class of disease
 * skin benign neoplasm Adnexal and skin appendage neoplasms epidermal appendage disease
 * neoplasms located in skin appendages
 * DOID:2433
 * epidermodysplasia verruciformis
 * class of disease
 * autosomal recessive disease viral infectious disease skin disease immune deficiency with skin involvement other immunodeficiency syndromes due to defects in innate immunity primary immunodeficiency disease disease
 * Human disease
 * DOID:13777
 * C01.925.256.650.810.345 C01.925.825.810.260 C01.925.928.914.345 C17.800.838.790.810.260
 * Epidermodysplasia verruciformis
 * World's 4th a Tree Man.jpg
 * epidermolysis bullosa acquisita
 * class of disease
 * epidermolysis bullosa pemphigoid bullous skin disease autoimmune skin disease
 * chronic subepidermal blistering disease associated with autoimmunity to type VII collagen
 * DOID:4313
 * C16.131.831.493.080 C17.800.804.493.080 C17.800.827.275.080 C17.800.865.410.080
 * epidermolysis bullosa herpetiformis
 * class of disease
 * epidermolysis bullosa simplex basal epidermolysis bullosa simplex genetic disease autosomal dominant disease
 * Human disease
 * DOID:0060735
 * epidermolysis bullosa with congenital localized absence of skin and deformity of nails
 * class of disease
 * dominant dystrophic epidermolysis bullosa autosomal dominant disease
 * human disease
 * DOID:0111347
 * epidermolytic acanthoma
 * class of disease
 * acanthoma
 * Human disease
 * DOID:4323
 * epidermolytic hyperkeratosis
 * class of disease
 * skin disease congenital ichthyosiform erythroderma keratinopathic ichthyosis
 * rare and severe form of ichthyosis
 * DOID:4603
 * C16.131.831.512.400.375 C16.320.850.400.375 C16.614.492.400.375 C17.800.428.333.250.375 C17.800.804.512.400.375 C17.800.827.400.375
 * Epidermolytic ichthyosis
 * Epidermolytic hyperkeratosis new image.jpg
 * epididymal neoplasm
 * class of disease
 * male reproductive system neoplasm epididymis disease testicular cancer
 * Human disease
 * DOID:512
 * epididymis adenocarcinoma
 * class of disease
 * epididymis cancer adenocarcinoma
 * epididymis cancer that derives from epithelial cells of glandular origin
 * DOID:10368
 * epididymis adenomatoid tumor
 * class of disease
 * male reproductive organ benign neoplasm adenomatoid tumor benign neoplasm of epididymis adenoma
 * Human disease
 * DOID:745
 * epididymis cancer
 * class of disease
 * male reproductive organ cancer epididymal neoplasm epididymis disease
 * Human disease
 * DOID:10366
 * epididymis disease
 * class of disease
 * male reproductive system disease
 * human disease
 * DOID:0080373
 * epidural abscess
 * class of disease
 * central nervous system disease abscess central nervous system cancer
 * human disease
 * DOID:11387
 * C01.207.300 C10.228.228.300 C10.228.228.709.350 C10.228.854.303 C01.207.709.350 C01.830.025.325
 * epidural neoplasm
 * class of disease
 * Spinal cord cancer
 * Human disease
 * DOID:3618
 * C04.588.614.250.803.342 C10.228.854.765.342 C10.551.240.750.200
 * epidural spinal canal angiolipoma
 * class of disease
 * angiolipoma epidural neoplasm cell type cancer spinal cord disease central nervous system organ benign neoplasm
 * Human disease
 * DOID:3617
 * epidural spinal canal meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:3809
 * epiglottis neoplasm
 * class of disease
 * supraglottis neoplasm neoplasm of hypopharynx
 * Human disease
 * DOID:7105
 * epilepsy
 * class of disease dictionary page in Wikipedia
 * encephalopathy disease
 * human neurological disease causing seizures
 * DOID:1826
 * C10.228.140.490
 * Epilepsy
 * Spike-waves.png
 * epilepsy, idiopathic generalized, susceptibility to, 8
 * class of disease
 * genetic disease rare genetic epilepsy generalized epilepsy
 * human disease
 * DOID:0111322
 * epiphora due to excess lacrimation
 * class of disease
 * excessive tearing
 * Human disease
 * DOID:14244
 * epiphora due to insufficient drainage
 * class of disease
 * excessive tearing
 * Human disease
 * DOID:13756
 * epiphyseal dysplasia, multiple, 6
 * class of disease
 * multiple epiphyseal dysplasia genetic disease multiple epiphyseal dysplasia due to collagen 9 anomaly autosomal dominant disease
 * human disease
 * DOID:0070301
 * epiretinal membrane
 * class of disease
 * retinal disease degeneration of macula and posterior pole
 * disease of the eye in response to changes in the vitreous humor or more rarely, diabetes
 * DOID:2006
 * C11.768.328
 * Epiretinal membrane
 * episcleritis periodica fugax
 * class of disease
 * scleral disease episcleritis
 * Human disease
 * DOID:12124
 * episodic kinesigenic dyskinesia 2
 * class of disease
 * dystonia genetic disease autosomal dominant disease
 * A dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in variation in the chromosome region 16q13-q22.1.
 * DOID:0090054
 * epithelial and subepithelial dystrophy
 * class of disease
 * corneal dystrophy
 * Human disease
 * DOID:0060440
 * epithelial malignant thymoma
 * class of disease
 * dendritic cell thymoma
 * Human disease
 * DOID:7926
 * epithelial predominant Wilms' tumor
 * class of disease
 * nephroblastoma
 * Human disease
 * DOID:5189
 * epithelial predominant pulmonary blastoma
 * class of disease
 * pulmonary blastoma
 * Human disease
 * DOID:4768
 * epithelial-myoepithelial carcinoma
 * class of disease
 * malignant epithelial tumor of salivary glands salivary gland cancer
 * Human disease
 * DOID:5309
 * Epithelial-myoepithelial carcinoma
 * epithelial-stromal TGFBI dystrophy
 * class of disease
 * corneal dystrophy stromal dystrophy
 * human disease
 * DOID:0060441
 * epithelioid cell melanoma
 * class of disease
 * melanoma
 * Human disease
 * DOID:4360
 * epithelioid cell synovial sarcoma
 * class of disease
 * synovial sarcoma monophasic synovial sarcoma
 * Human disease
 * DOID:5494
 * epithelioid inflammatory myofibroblastic sarcoma
 * class of disease
 * inflammatory myofibroblastic tumour
 * human disease
 * DOID:0080372
 * epithelioid leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5264
 * epithelioid malignant peripheral nerve sheath tumor
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:8353
 * epithelioid neurofibroma
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:5149
 * epithelioid sarcoma
 * class of disease
 * soft-tissue sarcoma connective tissue neoplasm sarcoma
 * human disease
 * DOID:6193
 * Epithelioid sarcoma
 * epithelioid trophoblastic tumor
 * class of disease
 * cervical uterine cancer lung cancer cell type cancer gestational trophoblastic disease trophoblastic neoplasm
 * Human disease
 * DOID:3593
 * epithelioid type angiomyolipoma
 * class of disease
 * angiomyolipoma
 * angiomyolipoma composed exclusively or predominantly by polygonal epithelioid cells with eosinophilic cytoplasm, often associated with cytologic atypia
 * DOID:3318
 * Epithelioid angiomyolipoma
 * epithelioma cuniculatum
 * class of disease
 * verrucous carcinoma Foot Dermatoses cutaneous squamous-cell carcinoma
 * Human disease
 * DOID:3751
 * epulis
 * class of disease
 * gingival overgrowth
 * Human disease
 * DOID:5337
 * Epulis
 * equatorial staphyloma
 * class of disease
 * scleral staphyloma
 * Human disease
 * DOID:13788
 * erectile dysfunction
 * class of disease symptom or sign
 * sexual dysfunction reproductive system symptom disease
 * form of sexual dysfunction in males
 * DOID:1875
 * C12.100.500.214 F03.835.400 C12.100.875.486 C12.200.294.214
 * Erectile dysfunction
 * Erectile dysfunction.jpg
 * erythema elevatum diutinum
 * class of disease
 * vasculitis reactive neutrophilic dermatose immune complex mediated vasculitis
 * vasculitis characterised by red, purple, brown or yellow papules (raised spot), plaques, or nodules, found on the backs of the hands, other extensor surfaces overlying joints, and on the buttocks
 * DOID:0060567
 * Erythema elevatum diutinum
 * erythema multiforme
 * class of disease
 * skin disease erythema allergy disease
 * skin disease that is a type of allergic reaction located in skin, which occurs in response to medications, infections, or illness
 * DOID:0050185
 * C17.800.229.400 C17.800.865.475
 * Erythema multiforme
 * erythema nodosum
 * class of disease
 * reactive neutrophilic dermatose clinical sign panniculitis disease
 * skin disease
 * DOID:0080750
 * C17.800.174.600.375 C17.800.229.413 C20.543.206.380.375 C25.100.468.380.375
 * Erythema nodosum
 * An introduction to dermatology (1905) ERYTHEMA NODOSUM.jpg
 * erythematosquamous dermatosis
 * class of disease
 * skin disease
 * Human disease
 * DOID:9097
 * erythrasma
 * class of disease
 * pyoderma Corynebacterium infection disease
 * Human disease
 * DOID:4131
 * C01.150.252.410.040.246.694 C01.150.252.819.320 C01.800.720.320 C17.800.838.765.320
 * Erythrasma
 * Erythrasma.jpg
 * erythrokeratodermia variabilis et progressiva 1
 * class of disease
 * autosomal dominant disease autosomal recessive disease erythrokeratodermia variabilis
 * An erythrokeratodermia variabilis that has material basis in heterozygous, homozygous, or compound heterozygous mutation in GJB3 on 1p34.3.
 * DOID:0111195
 * erythrokeratodermia variabilis et progressiva 2
 * class of disease
 * erythrokeratodermia variabilis autosomal dominant disease
 * human disease
 * DOID:0080248
 * erythrokeratodermia variabilis et progressiva 3
 * class of disease
 * erythrokeratodermia variabilis autosomal dominant disease
 * human disease
 * DOID:0080249
 * erythrokeratodermia variabilis et progressiva 4
 * class of disease
 * erythrokeratodermia variabilis
 * human disease
 * DOID:0080250
 * erythrokeratodermia variabilis et progressiva 5
 * class of disease
 * erythrokeratodermia variabilis autosomal recessive disease
 * human disease
 * DOID:0080251
 * erythrokeratodermia variabilis et progressiva 6
 * class of disease
 * erythrokeratodermia variabilis autosomal dominant disease
 * human disease
 * DOID:0080766
 * erythropoietin polycythemia
 * class of disease
 * acquired polycythemia
 * Human disease
 * DOID:2839
 * esophageal adenoid cystic carcinoma
 * class of disease
 * esophageal carcinoma
 * esophageal carcinoma that derives from epithelial cells of the salivary gland
 * DOID:4878
 * esophageal adenosquamous carcinoma
 * class of disease
 * adenosquamous carcinoma squamous cell carcinoma esophageal cancer
 * esophageal carcinoma that derives from squamous cells and gland-like cells
 * DOID:5625
 * esophageal basaloid squamous cell carcinoma
 * class of disease
 * basaloid squamous cell carcinoma esophageal cancer squamous cell carcinoma
 * Human disease
 * DOID:7051
 * esophageal cancer
 * class of disease
 * esophageal neoplasm esophageal disease gastrointestinal system cancer disease
 * gastrointestinal system cancer that is located in the esophagus
 * DOID:5041
 * Esophageal cancer
 * Esophageal adenoca.jpg
 * esophageal candidiasis
 * class of disease
 * candidiasis fungal esophagitis esophageal disease
 * candidiasis that involves fungal infection of the esophagus by Candida albicans in immunocompromised people, resulting in lesions, bleeding, painful swallowing and substernal pain
 * DOID:13146
 * Esophageal candidiasis
 * esophageal carcinoma
 * class of disease
 * esophageal cancer carcinoma
 * esophageal cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:1107
 * esophageal disease
 * class of disease
 * gastrointestinal system disease
 * gastrointestinal system disease that is located in the esophagus
 * DOID:6050
 * C06.405.117
 * Diseases and disorders of the esophagus
 * esophageal diverticulosis
 * class of disease
 * esophageal disease esophageal diverticulum
 * Human disease
 * DOID:13185
 * C06.405.117.136 C06.405.205.282.500.438
 * esophageal leukoplakia
 * class of disease
 * esophageal disease leukoplakia
 * Human disease
 * DOID:9021
 * esophageal neuroendocrine tumor
 * class of disease
 * esophageal cancer
 * Human disease
 * DOID:5784
 * esophageal varix
 * class of disease
 * vein disorder esophageal disease esophageal and gastric varices disease
 * Human disease
 * DOID:112
 * Esophageal varices
 * Esophageal varices - wale.jpg
 * esophagus adenocarcinoma
 * class of disease
 * esophageal carcinoma adenocarcinoma
 * esophageal carcinoma that derives from epithelial cells of glandular origin
 * DOID:4914
 * Adenocarcinomas of esophagus
 * esophagus carcinoma in situ
 * class of disease
 * in situ carcinoma esophageal disease
 * Human disease
 * DOID:9095
 * esophagus leiomyoma
 * class of disease
 * benign neoplasm of esophagus esophageal disease gastrointestinal system benign neoplasm
 * Human disease
 * DOID:960
 * esophagus leiomyosarcoma
 * class of disease
 * esophagus sarcoma
 * Human disease
 * DOID:5276
 * esophagus liposarcoma
 * class of disease
 * esophagus sarcoma liposarcoma esophageal cancer
 * Human disease
 * DOID:5694
 * esophagus small cell carcinoma
 * class of disease
 * esophageal carcinoma esophageal neuroendocrine tumor inherited neuroendocrine tumor small cell carcinoma
 * Human disease
 * DOID:7134
 * esophagus squamous cell carcinoma
 * class of disease
 * esophageal carcinoma squamous cell carcinoma
 * esophageal carcinoma that derives from epithelial squamous cells located in the esophagus
 * DOID:3748
 * Squamous-cell carcinoma of esophagus
 * esophagus squamous cell papilloma
 * class of disease
 * benign neoplasm of esophagus esophageal disease gastrointestinal system benign neoplasm
 * Human disease
 * DOID:959
 * Esophageal squamous papilloma
 * esophagus verrucous carcinoma
 * class of disease
 * esophagus squamous cell carcinoma verrucous carcinoma
 * Human disease
 * DOID:3747
 * esotropia
 * class of disease
 * strabismus
 * Esotropia is a strabismus in which the eye turns inward toward the nose
 * DOID:9840
 * C10.292.562.887.300 C11.590.810.400
 * Esotropia
 * Andre Filipe Teixeira Marques Esotropia.jpg
 * essential hypertension
 * class of disease
 * arterial hypertension disease
 * hypertension with no known cause, the most common type of hypertension
 * DOID:10825
 * C14.907.489.165
 * essential tremor 1
 * class of disease
 * autosomal dominant disease essential tremor
 * human disease
 * DOID:0111428
 * essential tremor 2
 * class of disease
 * autosomal dominant disease essential tremor
 * human disease
 * DOID:0111429
 * essential tremor 3
 * class of disease
 * essential tremor
 * human disease
 * DOID:0111430
 * essential tremor 4
 * class of disease
 * essential tremor autosomal dominant disease
 * human disease
 * DOID:0111431
 * essential tremor 5
 * class of disease
 * essential tremor autosomal dominant disease
 * human disease
 * DOID:0111432
 * esthesioneuroblastoma
 * class of disease
 * blastoma head and neck cancer olfactory nerve neoplasm disease
 * rare cancer of the nasal cavity
 * DOID:369
 * C04.557.465.625.600.590.650.550.150 C04.557.470.670.590.650.550.150 C04.557.580.625.600.590.650.550.150 C10.292.650.200
 * estrogen excess
 * class of disease
 * ovarian dysfunction
 * Human disease
 * DOID:14336
 * estrogen-receptor negative breast cancer
 * class of disease
 * breast cancer
 * Human disease
 * DOID:0060076
 * estrogen-receptor positive breast cancer
 * class of disease
 * breast cancer Hormone receptor positive breast tumor
 * Human disease
 * DOID:0060075
 * ethmoid sinus adenocarcinoma
 * class of disease
 * ethmoid sinus cancer adenocarcinoma
 * ethmoid sinus cancer that derives from epithelial cells of glandular origin
 * DOID:2766
 * ethmoid sinus cancer
 * class of disease
 * paranasal sinus cancer ethmoidal sinus neoplasm
 * Human disease
 * DOID:1363
 * ethmoid sinus squamous cell carcinoma
 * class of disease
 * ethmoid sinus cancer squamous cell carcinoma
 * Human disease
 * DOID:2763
 * ethmoid sinusitis
 * class of disease
 * sinusitis
 * sinusitis which involves infection of ethmoid sinuses that causes pain or pressure behind and between the eyes, tearing, and headache over the forehead
 * DOID:9507
 * C08.460.692.752.267 C08.730.749.267 C09.603.692.752.267 C01.748.749.267
 * ethmoidal sinus neoplasm
 * class of disease
 * paranasal sinus neoplasm
 * Human disease
 * DOID:1364
 * eumycotic mycetoma
 * class of disease
 * dermatomycosis mycetoma disease
 * chronic granulomatous fungal disease of humans
 * DOID:13078
 * Madura foot
 * Madura foot..JPG
 * eunuchism
 * class of disease
 * hypogonadism, male hypogonadism disease
 * hypogonadism that is characterized by the lack of mature male germ cells and testicular hormones
 * DOID:5003
 * C19.391.482.293
 * Eunuchoidism
 * euthyroid sick syndrome
 * class of disease
 * thyroid gland disease
 * Secondary allostasis of thyroid function in fetal life, starving and in critical illness
 * DOID:2856
 * C19.874.255
 * eversion of lacrimal punctum
 * class of disease
 * lacrimal apparatus disease
 * Human disease
 * DOID:13651
 * exanthem
 * class of disease symptom or sign
 * skin disease rash disease
 * human disease
 * DOID:0050486
 * C17.800.257
 * Exanthem
 * Severerash.jpg
 * exanthema subitum
 * class of disease
 * viral infectious disease Roseolovirus infectious disease disease
 * Human disease
 * DOID:0050495
 * C01.925.256.466.850.290 C01.925.825.290 C17.800.257.335 C17.800.838.790.290
 * Roseola
 * Hhv-6 (1).jpg
 * excessive tearing
 * class of disease symptom or sign
 * lacrimal apparatus disease tear secretion eye symptom disease
 * overflow of tears onto the face
 * DOID:13757
 * Epiphora (medicine)
 * excoriation
 * class of disease symptom or sign
 * dermatitis disease
 * human disease
 * DOID:9165
 * exercise-induced bronchoconstriction
 * class of disease
 * asthma dyspnea on effort intrinsic asthma
 * medical condition
 * DOID:0080821
 * C08.127.108.110 C08.674.095.110 C20.543.480.680.095.110
 * exfoliation syndrome
 * class of disease
 * iris disease hereditary glaucoma phacogenic glaucoma
 * syndrome that occurs when tiny flakes of dandruff-like material build up in the body and are found in the heart, kidneys, liver, lungs, and eye
 * DOID:13641
 * C11.941.375.285
 * exocervical carcinoma
 * class of disease
 * cervix carcinoma
 * Human disease
 * DOID:2892
 * exocrine pancreatic insufficiency
 * class of disease
 * pancreas disease
 * Human disease
 * DOID:13316
 * C06.689.276
 * exophthalmic ophthalmoplegia
 * class of disease
 * ophthalmoplegia
 * Human disease
 * DOID:13135
 * exostosis
 * class of disease
 * hyperostosis
 * hyperostosis that involves formation of new bone on the surface of preexisting bone
 * DOID:203
 * C05.116.540.310
 * Exostoses
 * Exostose Femur 54jm- CT cor und VR - 001.svg
 * exotropia
 * class of disease
 * strabismus
 * form of strabismus where the eyes are deviated outward
 * DOID:1143
 * C10.292.562.887.650 C11.590.810.440
 * Exotropia
 * exposure keratitis
 * class of disease
 * keratoconjunctivitis
 * Human disease
 * DOID:9461
 * expressive language disorder
 * class of disease
 * language disorder specific language impairment-5
 * neurodevelopmental condition
 * DOID:11385
 * external auditory meatus lipoma
 * class of disease
 * sensory organ benign neoplasm lipoma external ear neoplasm benign neoplasm of ear
 * Human disease
 * DOID:10203
 * external resorption
 * class of disease
 * tooth resorption
 * human disease
 * DOID:14529
 * extra-adrenal pheochromocytoma
 * class of disease
 * malignant pheochromocytoma
 * adrenal medulla cancer that originate in the ganglia of the sympathetic nervous system and are named based upon the primary anatomical site of origin
 * DOID:0050936
 * extracranial neuroblastoma
 * class of disease
 * neuroblastoma
 * Human disease
 * DOID:371
 * extracutaneous mastocytoma
 * class of disease
 * systemic mastocytosis mastocytoma connective tissue neoplasm benign mastocytoma genetic hematologic disease rare genetic immune disease inherited tumor rare genetic bone disease
 * Human disease
 * DOID:4659
 * extragonadal germ cell cancer
 * class of disease
 * germ cell cancer extragonadal germ cell tumor
 * A germ cell cancer that derives from germ cells that are found in areas of the body other than the ovary or testicle. The tumors originate in the sperm forming cells in the testicles or egg producing cells in the ovary.
 * DOID:4717
 * extragonadal nonseminomatous germ cell tumor
 * class of disease
 * extragonadal germ cell cancer brain cancer mediastinal cancer extragonadal non-dysgerminomatous germ cell tumor germ cell cancer nongerminomatous germ cell tumor
 * extragonadal germ cell cancer that are located in the pineal gland in the brain, located in the mediastinum or located in the abdomen
 * DOID:5677
 * extragonadal seminoma
 * class of disease
 * seminoma
 * Human disease
 * DOID:5838
 * extrahepatic bile duct adenocarcinoma
 * class of disease
 * extrahepatic bile duct carcinoma adenocarcinoma bile duct adenocarcinoma
 * extrahepatic bile duct carcinoma that derives from epithelial cells of glandular origin
 * DOID:3495
 * extrahepatic bile duct adenoma
 * class of disease
 * bile duct adenoma biliary tract neoplasm
 * bile duct ademona and neoplasm of extrahepatic bile duct that are composed of papillary, tubular, or combined tubulopapillary structures lined by dysplastic epithelium
 * DOID:5438
 * extrahepatic bile duct carcinoma
 * class of disease
 * bile duct carcinoma bile duct cancer
 * Human disease
 * DOID:4682
 * extrahepatic bile duct cystadenoma
 * class of disease
 * bile duct cystadenoma extrahepatic bile duct adenoma
 * Human disease
 * DOID:8105
 * extrahepatic bile duct leiomyoma
 * class of disease
 * leiomyoma bile duct disease biliary tract neoplasm liver leiomyoma
 * Human disease
 * DOID:5125
 * extrahepatic bile duct leiomyosarcoma
 * class of disease
 * bile duct sarcoma leiomyosarcoma extrahepatic bile duct carcinoma liver leiomyosarcoma
 * leiomyosarcoma and sarcoma of bile duct that is located in the bile duct or located in the outside of the liver
 * DOID:5293
 * extrahepatic bile duct lipoma
 * class of disease
 * biliary tract neoplasm lipoma bile duct disease liver lipoma
 * human disease
 * DOID:10209
 * extrahepatic bile duct papillary adenoma
 * class of disease
 * extrahepatic bile duct adenoma biliary papillomatosis
 * Human disease
 * DOID:7503
 * extrahepatic bile duct small cell adenocarcinoma
 * class of disease
 * extrahepatic bile duct adenocarcinoma liver neuroendocrine carcinoma
 * Human disease
 * DOID:5926
 * extrahepatic biliary papillomatosis
 * class of disease
 * biliary papillomatosis
 * Human disease
 * DOID:7752
 * extrahepatic cholestasis
 * class of disease
 * cholestasis non-neoplastic bile duct disorder
 * Human disease
 * DOID:13619
 * C06.130.120.135.150
 * extramedullary plasmacytoma
 * class of disease
 * plasmacytoma
 * Human disease
 * DOID:3720
 * extranodal NK/T-cell lymphoma, nasal type
 * class of disease
 * T-cell lymphoma mature T-cell and NK-cell lymphoma nasal cavity cancer
 * medical condition
 * DOID:0080797
 * C04.557.386.480.750.199
 * extraosseous Ewing's sarcoma
 * class of disease
 * Ewing sarcoma
 * Human disease
 * DOID:4232
 * extraosseous Ewings sarcoma-primitive neuroepithelial tumor
 * class of disease
 * extraosseous Ewing's sarcoma
 * Human disease
 * DOID:4985
 * extraosseous chondrosarcoma
 * class of disease
 * chondrosarcoma
 * chondrosarcoma that is located in exclusively soft tissue
 * DOID:4549
 * extraosseous osteosarcoma
 * class of disease
 * osteosarcoma connective tissue neoplasm
 * Human disease
 * DOID:3357
 * extrapulmonary tuberculosis
 * class of disease
 * tuberculosis
 * respiratory disease
 * DOID:0050598
 * C01.150.252.410.040.552.846.617
 * Extrapulmonary tuberculosis
 * Mal de POTT esp.jpg
 * extrapyramidal and movement disorder
 * class of disease
 * movement disorders neurological disorder
 * disease of the nervous system
 * DOID:13839
 * extraskeletal chondroma
 * class of disease
 * connective tissue benign neoplasm
 * Human disease
 * DOID:3814
 * extraskeletal mesenchymal chondrosarcoma
 * class of disease
 * extraosseous chondrosarcoma mesenchymal chondrosarcoma
 * Human disease
 * DOID:4548
 * extraskeletal myxoid chondrosarcoma
 * class of disease
 * extraosseous chondrosarcoma myxoid chondrosarcoma
 * extraosseous chondrosarcoma that has material basis in cells derived from transformed cells that produce cartilage and is characterized by a marked abundance of extracellular mucoid (myxoid) matrix
 * DOID:6496
 * extratemporal epilepsy
 * class of disease
 * epilepsy focal epilepsy
 * epilepsy syndrome that is located in an area of the brain other than the temporal lobe
 * DOID:2544
 * extrinsic allergic alveolitis
 * class of disease symptom or sign
 * occupational disease interstitial lung disease allergy disease
 * human disease
 * DOID:841
 * C08.381.483.125 C08.674.055 C20.543.480.680.075
 * Hypersensitivity pneumonitis
 * Chronic hypersensitivity pneumonitis - histology.jpg
 * extrinsic asthma
 * class of disease
 * chronic asthma allergy
 * human disease
 * DOID:0080811
 * exudative glomerulonephritis
 * class of disease
 * glomerulonephritis
 * Human disease
 * DOID:4777
 * exudative vitreoretinopathy 1
 * class of disease
 * exudative vitreoretinopathy autosomal dominant disease
 * human disease
 * DOID:0111412
 * exudative vitreoretinopathy 3
 * class of disease
 * exudative vitreoretinopathy autosomal dominant disease
 * human disease
 * DOID:0111409
 * exudative vitreoretinopathy 4
 * class of disease
 * exudative vitreoretinopathy autosomal genetic disease
 * human disease
 * DOID:0111411
 * exudative vitreoretinopathy 5
 * class of disease
 * exudative vitreoretinopathy autosomal dominant disease
 * human disease
 * DOID:0111408
 * exudative vitreoretinopathy 6
 * class of disease
 * exudative vitreoretinopathy autosomal dominant disease
 * human disease
 * DOID:0111410
 * exudative vitreoretinopathy 7
 * class of disease
 * exudative vitreoretinopathy autosomal dominant disease
 * human disease
 * DOID:0080264
 * eye accommodation disease
 * class of disease
 * eye disease refraction or accommodation disorder
 * Human disease
 * DOID:10034
 * eye carcinoma
 * class of disease
 * ocular cancer carcinoma
 * ocular cancer that has material basis in abnormally proliferating cells, derives from epithelial cells and arises from the tissues that cover structures located in the eye
 * DOID:295
 * eye degenerative disease
 * class of disease
 * eye disease degenerative disease
 * neurodegenerative disease that involves the eye
 * DOID:9799
 * eye disease
 * class of disease
 * eye and adnexa disease sensory system disease organ-specific disease
 * health condition negatively affecting the eye
 * DOID:5614
 * C11
 * Diseases and disorders of the eye and adnexa
 * eyelid disease
 * class of disease
 * eye adnexa disease skin disease
 * adnexa disease that is located in the eyelid
 * DOID:530
 * C11.338
 * eyelid neoplasm
 * class of disease
 * skin neoplasm eyelid disease facial neoplasm skin benign neoplasm
 * human disease
 * DOID:2173
 * C04.588.443.392.500 C11.319.421 C11.338.526
 * facial dermatosis
 * class of disease
 * skin disease head and neck disease
 * Human disease
 * DOID:3134
 * C17.800.271
 * facial nerve disease
 * class of disease
 * cranial nerve disease
 * human disease
 * DOID:1756
 * C07.465.299 C10.292.319
 * facial nerve neoplasm
 * class of disease
 * cranial nerve neoplasm facial nerve disease
 * Human disease
 * DOID:1760
 * Facial nerve neoplasms
 * facial neuralgia
 * class of disease
 * neuralgia facial nerve disease orofacial pain cranial neuralgia
 * human disease
 * DOID:13865
 * C07.465.299.625 C10.292.319.625
 * facioscapulohumeral muscular dystrophy
 * class of disease
 * muscular dystrophy disease
 * Muscular dystrophy that classically weakens the muscles of the face (facio), shoulder girdle (scapulo) and upper arm (humerus). Weakness usually is asymmetrical and develops in other areas of the body as well, such as the abdomen and shin.
 * DOID:11727
 * C05.651.534.500.400 C10.668.491.175.500.400 C16.320.577.400
 * Facioscapulohumeral muscular dystrophy
 * facioscapulohumeral muscular dystrophy 1
 * class of disease
 * facioscapulohumeral muscular dystrophy
 * facioscapulohumeral muscular dystrophy that has material basis in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35
 * DOID:0111192
 * facioscapulohumeral muscular dystrophy 2
 * class of disease
 * digenic disease facioscapulohumeral muscular dystrophy
 * A facioscapulohumeral muscular dystrophy that has material basis in digenic inheritance of a heterozygous mutation in SMCHDI on 18p11.32 and a haplotype on chromosome 4 that is permissive for DUX4 expression.
 * DOID:0111193
 * factitious disorder
 * class of disease
 * mental disorder
 * disease of mental health where symptoms are deliberately produced, feigned or exaggerated in order to falsely demonstrate the presence of an illness
 * DOID:1766
 * F03.875.375
 * Factitious disorders
 * factor VII deficiency
 * class of disease
 * inherited blood coagulation disease blood coagulation disease autosomal recessive disease
 * Human disease
 * DOID:2215
 * C15.378.100.100.310 C15.378.100.141.310 C15.378.463.310 C16.320.099.310
 * factor X deficiency
 * class of disease
 * inherited blood coagulation disease blood coagulation disease autosomal recessive disease
 * Human disease
 * DOID:2222
 * C15.378.100.100.320 C15.378.100.141.320 C15.378.463.320 C16.320.099.320
 * fallopian tube adenocarcinoma
 * class of disease
 * fallopian tube carcinoma adenocarcinoma
 * fallopian tube carcinoma that derives from epithelial cells of glandular origin
 * DOID:3706
 * fallopian tube adenofibroma
 * class of disease
 * fallopian tube benign neoplasm adenofibroma serous adenofibroma
 * Human disease
 * DOID:5478
 * fallopian tube adenomatoid tumor
 * class of disease
 * fallopian tube benign neoplasm adenomatoid tumor adenoma
 * Human disease
 * DOID:5196
 * Adenomatoid tumor of fallopian tube
 * fallopian tube adenosarcoma
 * class of disease
 * fallopian tube carcinosarcoma
 * Human disease
 * DOID:1973
 * fallopian tube benign neoplasm
 * class of disease
 * female reproductive organ benign neoplasm fallopian tube neoplasm fallopian tube disease
 * Human disease
 * DOID:0060111
 * fallopian tube cancer
 * class of disease
 * female reproductive organ cancer fallopian tube neoplasm fallopian tube disease
 * female reproductive organ cancer that is located in fallopian tube
 * DOID:1964
 * Fallopian tube cancer
 * fallopian tube carcinoma
 * class of disease
 * fallopian tube cancer carcinoma
 * fallopian tube cancer that is located in the fallopian tube
 * DOID:1963
 * fallopian tube carcinosarcoma
 * class of disease
 * fallopian tube cancer
 * fallopian tube cancer that is characterized as a mixture of carcinoma and sarcoma and has material basis in epithelial tissue and has material basis in connective tissue
 * DOID:1970
 * fallopian tube clear cell adenocarcinoma
 * class of disease
 * fallopian tube adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5301
 * fallopian tube cystadenofibroma
 * class of disease
 * fallopian tube adenofibroma cystadenofibroma
 * Human disease
 * DOID:8211
 * fallopian tube disease
 * class of disease
 * female reproductive system disease adnexal disease
 * Human disease
 * DOID:1962
 * C13.351.500.056.390
 * Diseases and disorders of fallopian tubes
 * fallopian tube endometrioid adenocarcinoma
 * class of disease
 * fallopian tube adenocarcinoma
 * Human disease
 * DOID:5831
 * fallopian tube endometriosis
 * class of disease
 * fallopian tube disease endometriosis
 * human disease
 * DOID:11424
 * Endometriosis of fallopian tube
 * fallopian tube germ cell cancer
 * class of disease
 * fallopian tube cancer germ cell cancer
 * Human disease
 * DOID:5324
 * fallopian tube gestational choriocarcinoma
 * class of disease
 * fallopian tube carcinoma gestational choriocarcinoma fallopian tube germ cell cancer familiar fallopian tube carcinoma
 * Human disease
 * DOID:8186
 * fallopian tube leiomyoma
 * class of disease
 * fallopian tube benign neoplasm leiomyoma
 * Human disease
 * DOID:5124
 * fallopian tube leiomyosarcoma
 * class of disease
 * fallopian tube cancer leiomyosarcoma
 * Human disease
 * DOID:1965
 * fallopian tube mucinous adenocarcinoma
 * class of disease
 * fallopian tube adenocarcinoma fallopian tube mucinous tumor mucinous adenocarcinoma
 * human disease
 * DOID:3704
 * fallopian tube mucinous tumor
 * class of disease
 * fallopian tube benign neoplasm mucinous tumor fallopian tube cancer
 * Human disease
 * DOID:3705
 * fallopian tube papillary adenocarcinoma
 * class of disease
 * fallopian tube adenocarcinoma
 * Human disease
 * DOID:5597
 * fallopian tube serous adenocarcinoma
 * class of disease
 * fallopian tube adenocarcinoma serous cystadenocarcinoma
 * Human disease
 * DOID:5598
 * fallopian tube serous papilloma
 * class of disease
 * fallopian tube benign neoplasm
 * Human disease
 * DOID:3173
 * fallopian tube squamous cell carcinoma
 * class of disease
 * fallopian tube carcinoma squamous cell carcinoma
 * Human disease
 * DOID:5540
 * fallopian tube teratoma
 * class of disease
 * fallopian tube germ cell cancer fallopian tube cancer
 * Human disease
 * DOID:5564
 * fallopian tube transitional cell carcinoma
 * class of disease
 * fallopian tube carcinoma transitional cell carcinoma
 * Human disease
 * DOID:4008
 * familial GPIHBP1 deficiency
 * class of disease
 * autosomal recessive disease familial chylomicronemia syndrome hyperlipoproteinemia type I
 * human disease
 * DOID:0111420
 * familial adenomatous polyposis 1
 * class of disease
 * familial adenomatous polyposis autosomal dominant disease
 * familial adenomatous polyposis that has material basis in heterozygous mutation in the APC gene on chromosome 5q22
 * DOID:0080409
 * familial adenomatous polyposis 2
 * class of disease
 * familial adenomatous polyposis autosomal recessive disease
 * familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the MUTYH gene on chromosome 1p34
 * DOID:0080410
 * familial adenomatous polyposis 3
 * class of disease
 * familial adenomatous polyposis
 * familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the NTHL1 gene on chromosome 16p13
 * DOID:0080411
 * familial adult myoclonic epilepsy 4
 * class of disease
 * myoclonic epilepsy benign adult familial myoclonic epilepsy autosomal dominant disease
 * human disease
 * DOID:0111693
 * familial adult myoclonic epilepsy 6
 * class of disease
 * autosomal dominant disease benign adult familial myoclonic epilepsy
 * human disease
 * DOID:0111696
 * familial adult myoclonic epilepsy 7
 * class of disease
 * benign adult familial myoclonic epilepsy autosomal dominant disease
 * human disease
 * DOID:0111694
 * familial bicuspid aortic valve
 * class of disease
 * bicuspid aortic valve aortic valve disease
 * human disease
 * DOID:0080332
 * familial chronic myelocytic leukemia-like syndrome
 * class of disease
 * chronic myeloid leukemia
 * chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome)
 * DOID:0060761
 * familial chylomicronemia due to inhibition of lipoprotein lipase activity
 * class of disease
 * familial chylomicronemia syndrome hyperlipoproteinemia type I
 * human disease
 * DOID:0111419
 * familial chylomicronemia syndrome
 * class of disease
 * hyperlipidemia familial hyperlipidemia Primary hyperchylomicronemia
 * human disease
 * DOID:0111417
 * familial cold autoinflammatory syndrome 1
 * class of disease
 * familial cold urticaria genetic disease
 * familial cold autoinflammatory syndrome characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the NLRP gene on chromosome 1q44
 * DOID:0090062
 * familial episodic pain syndrome
 * class of disease
 * neuropathic pain peripheral neuropathy
 * human disease
 * DOID:0111728
 * familial episodic pain syndrome 1
 * class of disease
 * familial episodic pain syndrome autosomal dominant disease
 * human disease
 * DOID:0111729
 * familial episodic pain syndrome 2
 * class of disease
 * familial episodic pain syndrome autosomal dominant disease
 * human disease
 * DOID:0111730
 * familial episodic pain syndrome 3
 * class of disease
 * familial episodic pain syndrome autosomal dominant disease
 * human disease
 * DOID:0111731
 * familial erythrocytosis 1
 * class of disease
 * primary polycythemia autosomal dominant disease
 * Human disease
 * DOID:0060652
 * familial erythrocytosis 3
 * class of disease
 * primary polycythemia autosomal dominant disease
 * human disease
 * DOID:0080338
 * familial erythrocytosis 4
 * class of disease
 * primary polycythemia
 * human disease
 * DOID:0080339
 * familial erythrocytosis 5
 * class of disease
 * primary polycythemia autosomal dominant disease
 * human disease
 * DOID:0080290
 * familial erythrocytosis 6
 * class of disease
 * primary polycythemia
 * human disease
 * DOID:0111632
 * familial erythrocytosis 7
 * class of disease
 * primary polycythemia
 * human disease
 * DOID:0111631
 * familial febrile seizures 1
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111307
 * familial febrile seizures 10
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111304
 * familial febrile seizures 11
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111308
 * familial febrile seizures 2
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111310
 * familial febrile seizures 4
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111305
 * familial febrile seizures 5
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111306
 * familial febrile seizures 6
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111309
 * familial febrile seizures 7
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111311
 * familial febrile seizures 8
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111298
 * familial febrile seizures 9
 * class of disease
 * febrile seizures, familial
 * human disease
 * DOID:0111303
 * familial glomangioma
 * class of disease
 * glomangioma rare circulatory system disease inherited renal tumor cardiovascular cancer inherited soft tissue tumor
 * Human disease
 * DOID:7996
 * familial glucocorticoid deficiency
 * class of disease
 * adrenal gland disease
 * human disease
 * DOID:0080620
 * familial hemiplegic migraine 1
 * class of disease
 * familial hemiplegic migraine
 * familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has material basis in heterozygous mutation in CACNA1A on 19p13
 * DOID:0111181
 * familial hemiplegic migraine 2
 * class of disease
 * familial hemiplegic migraine
 * A familial hemiplegic migraine that has material basis in heterozygous mutation in ATP1A2 on 1q23.2.
 * DOID:0111182
 * familial hemiplegic migraine 3
 * class of disease
 * familial hemiplegic migraine
 * A familial hemiplegic migraine that has material basis in heterozygous mutation in SCN1A on 2q24.3.
 * DOID:0111183
 * familial hemophagocytic lymphohistiocytosis 1
 * class of disease
 * familial hemophagocytic lymphohistiocytosis genetic disease hemophagocytic lymphohistiocytosis autosomal recessive disease
 * A hemophagocytic lymphohistiocytosis that has material basis in an autosomal recessive mutation of HPLH1 on chromosome 9q21.3-q22.
 * DOID:0110921
 * familial hepatic adenoma
 * class of disease
 * autosomal recessive disease hepatocellular adenoma
 * human disease
 * DOID:0111366
 * familial hyperinsulinemic hypoglycemia 1
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has material basis in mutation in the ABCC8 gene on chromosome 11p15
 * DOID:0070219
 * familial hyperinsulinemic hypoglycemia 2
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of severe hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has material basis in mutation in the KCNJ11 gene on chromosome 11p15.1.
 * DOID:0070218
 * familial hyperinsulinemic hypoglycemia 3
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * human disease
 * DOID:0070216
 * familial hyperinsulinemic hypoglycemia 4
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia with seizures that has material basis in mutation in the HADH gene on chromosome 4q25
 * DOID:0070215
 * familial hyperinsulinemic hypoglycemia 5
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * human disease
 * DOID:0070220
 * familial hyperinsulinemic hypoglycemia 6
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * human disease
 * DOID:0070217
 * familial hyperinsulinemic hypoglycemia 7
 * class of disease
 * hyperinsulinemic hypoglycemia genetic disease
 * A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has material basis in mutation in the SLC16A1 gene on chromosome 1p13.2.
 * DOID:0070214
 * familial hyperlipidemia
 * class of disease
 * lipid metabolism disorder hyperlipidemia
 * Human disease
 * DOID:1168
 * familial hypertrophic cardiomyopathy
 * class of disease
 * hypertrophic cardiomyopathy familial cardiomyopathy
 * Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions
 * DOID:0080326
 * C14.280.238.100.500 C14.280.484.150.070.160.500 C16.320.160
 * familial hypertryptophanemia
 * class of disease
 * amino acid metabolic disorder autosomal recessive disease hypertryptophanemia
 * human disease
 * DOID:0111703
 * familial hypobetalipoproteinemia 1
 * class of disease
 * hypobetalipoproteinemia
 * hypobetalipoproteinemia that has material basis in mutation in the APOB gene on chromosome 2p24
 * DOID:0111062
 * familial hypobetalipoproteinemia 2
 * class of disease
 * hypobetalipoproteinemia
 * hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31
 * DOID:0111061
 * familial hypocalciuric hypercalcemia 1
 * class of disease
 * familial hypocalciuric hypercalcemia genetic disease
 * familial hypocalciuric hypercalcemia that has material basis in heterozygous loss-of-function mutations in the CASR gene on chromosome 3q21
 * DOID:0060700
 * familial isolated trichomegaly
 * class of disease
 * Trichomegaly eyelid disease autosomal recessive disease
 * DOID:0111566
 * familial lipase maturation factor 1 deficiency
 * class of disease
 * familial chylomicronemia syndrome autosomal recessive disease
 * human disease
 * DOID:0111422
 * familial lipoprotein lipase deficiency
 * class of disease
 * hyperlipoproteinemia type I autosomal recessive disease familial chylomicronemia syndrome
 * familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides
 * DOID:14118
 * familial melanoma
 * class of disease
 * melanoma
 * Human disease
 * DOID:6846
 * familial meningioma
 * class of disease
 * meningioma hereditary neoplastic syndromes
 * Human disease
 * DOID:4586
 * familial multiple nevi flammei
 * class of disease
 * capillary disease port-wine stain
 * human disease
 * DOID:0111529
 * familial nephrotic syndrome
 * class of disease
 * nephrotic syndrome genetic disease monogenic disease
 * Human disease
 * DOID:2590
 * familial partial lipodystrophy type 1
 * class of disease
 * familial partial lipodystrophy
 * familial partial lipodystrophy characterized by loss of adipose tissue that is confined to the extremities with normal or increased fat in other areas of the body
 * DOID:0070207
 * familial partial lipodystrophy type 2
 * class of disease
 * familial partial lipodystrophy genetic disease autosomal dominant disease
 * familial partial lipodystrophy characterized by autosomal dominant inheritance of loss of subcutaneous fat from the limbs and trunk that has material basis in mutation in the LMNA gene on chromosome 1q21
 * DOID:0070202
 * familial partial lipodystrophy type 3
 * class of disease
 * familial partial lipodystrophy genetic disease autosomal dominant disease
 * familial partial lipodystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the PPARG gene on chromosome 3p25
 * DOID:0070204
 * familial partial lipodystrophy type 6
 * class of disease
 * familial partial lipodystrophy genetic disease autosomal recessive disease
 * familial partial lipodystrophy characterized by autosomal recessive inheritance that has material basis in mutation in the LIPE gene on chromosome 19q13
 * DOID:0070206
 * familial progressive hyper- and hypopigmentation
 * class of disease
 * autosomal dominant disease skin disease familial progressive hyperpigmentation
 * human disease
 * DOID:0111373
 * familial renal oncocytoma
 * class of disease
 * renal oncocytoma inherited renal tumor
 * Human disease
 * DOID:6244
 * familial renal papillary carcinoma
 * class of disease
 * hereditary renal cell carcinoma
 * Human disease
 * DOID:6163
 * familial retinoblastoma
 * class of disease
 * retinoblastoma hereditary neoplastic syndromes
 * Human disease
 * DOID:4648
 * familial temporal lobe epilepsy 2
 * class of disease
 * temporal lobe epilepsy genetic disease autosomal dominant disease
 * A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has material basis in variation in the chromosome region 12q22-q23.3.
 * DOID:0060755
 * familial temporal lobe epilepsy 3
 * class of disease
 * temporal lobe epilepsy genetic disease autosomal dominant disease
 * A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has material basis in variation in the chromosome region 4q13.2-q21.3.
 * DOID:0060750
 * familial temporal lobe epilepsy 4
 * class of disease
 * temporal lobe epilepsy genetic disease autosomal dominant disease
 * temporal lobe epilepsy characterized by autosomal dominant inheritance of occipitotemporal lobe epilepsy and migraine with visual aura and that has material basis in variation in the chromosome region 9q21-q22
 * DOID:0060753
 * familial temporal lobe epilepsy 6
 * class of disease
 * temporal lobe epilepsy genetic disease autosomal dominant disease
 * temporal lobe epilepsy that has material basis in variation in the chromosome region 3q25-q26
 * DOID:0060749
 * familial temporal lobe epilepsy 7
 * class of disease
 * temporal lobe epilepsy genetic disease familial partial epilepsy autosomal dominant disease
 * temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22
 * DOID:0060751
 * familial temporal lobe epilepsy 8
 * class of disease
 * temporal lobe epilepsy genetic disease autosomal dominant disease
 * temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13
 * DOID:0060754
 * familial thyroid dyshormonogenesis
 * class of disease
 * congenital hypothyroidism
 * human disease
 * DOID:0112183
 * familiar fallopian tube carcinoma
 * class of disease
 * fallopian tube carcinoma inherited gynecological tumor
 * Human disease
 * DOID:7266
 * familiar ovarian carcinoma
 * class of disease
 * surface epithelial-stromal tumor ovarian cancer carcinoma
 * Human disease
 * DOID:6901
 * farmer's lung
 * class of disease
 * extrinsic allergic alveolitis disease
 * hypersensitivity pneumonitis
 * DOID:14453
 * C08.381.483.125.365 C08.674.055.365 C20.543.480.680.075.365 C24.080.365
 * fasciitis
 * class of disease
 * connective tissue disease disease
 * Inflammation process in fascia
 * DOID:9598
 * C05.321
 * Fasciitis
 * fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1
 * class of disease
 * autosomal recessive disease fatal infantile encephalocardiomyopathy
 * fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in compound heterozygous mutation in the SCO2 gene on chromosome 22q13
 * DOID:0080357
 * fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3
 * class of disease
 * autosomal recessive disease fatal infantile encephalocardiomyopathy
 * fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous mutation in the COA5 gene on chromosome 2q11
 * DOID:0080359
 * fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4
 * class of disease
 * fatal infantile encephalocardiomyopathy autosomal recessive disease
 * fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous or compound heterozygous mutation in the COA6 gene on chromosome 1q42
 * DOID:0080360
 * fatal multiple mitochondrial dysfunctions syndrome
 * class of disease
 * mitochondrial disease
 * mitochondrial metabolism disease that is characterized by variants in genes involved in mitochondrial energy production, resulting in impairment of energy production at more than one stage of energy metabolism
 * DOID:0070330
 * fatty liver disease
 * class of disease
 * lipid storage disease disease
 * lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis
 * DOID:9452
 * C06.552.241
 * Fatty liver
 * favism
 * class of disease
 * glucose-6-phosphate dehydrogenase deficiency
 * glucosephosphate dehydrogenase deficiency characterized by a hemolytic reaction to consumption of broad beans
 * DOID:13628
 * C15.378.071.141.150.480.370 C15.378.071.141.370 C16.320.070.480.370 C25.723.415.341 C25.723.756.375
 * febrile neutrophilic dermatosis
 * class of disease
 * reactive neutrophilic dermatose erythema rare rheumatologic disease other acquired skin disease skin disease allergy disease
 * skin disease
 * DOID:0080746
 * C17.800.229.800
 * Febrile neutrophilic dermatosis
 * febrile seizures, familial
 * class of disease
 * febrile seizure encephalopathy
 * human disease
 * DOID:0111297
 * feline panleukopenia
 * class of disease
 * parvovirus infectious disease cat disease
 * cat disease
 * DOID:3799
 * C01.925.256.700.363 C22.180.460
 * female breast axillary tail cancer
 * class of disease
 * female breast cancer
 * Human disease
 * DOID:1650
 * female breast cancer
 * class of disease
 * breast cancer
 * Human disease
 * DOID:0050671
 * female breast carcinoma
 * class of disease
 * breast carcinoma
 * breast carcinoma that is manifested in the female breast
 * DOID:7843
 * female breast central part cancer
 * class of disease
 * female breast cancer
 * human disease
 * DOID:13799
 * female breast lower-inner quadrant cancer
 * class of disease
 * female breast cancer
 * Human disease
 * DOID:1649
 * female breast lower-outer quadrant cancer
 * class of disease
 * female breast cancer
 * Human disease
 * DOID:13972
 * female breast upper-inner quadrant cancer
 * class of disease
 * female breast cancer
 * Human disease
 * DOID:1647
 * female breast upper-outer quadrant cancer
 * class of disease
 * female breast cancer
 * Human disease
 * DOID:9773
 * female infertility of uterine origin
 * class of disease
 * uterine disease female infertility
 * Human disease
 * DOID:13589
 * female reproductive endometrioid cancer
 * class of disease
 * female reproductive organ cancer Endometrioid tumor
 * human disease
 * DOID:3001
 * female reproductive organ benign neoplasm
 * class of disease
 * reproductive organ benign neoplasm female reproductive system disease
 * human disease
 * DOID:0060086
 * female reproductive organ cancer
 * class of disease
 * female reproductive system disease reproductive organ cancer female reproductive system neoplasm
 * human disease
 * DOID:120
 * Cancers of female genital organs
 * female reproductive system disease
 * class of disease
 * reproductive system disease female urogenital disease
 * reproductive system disease that impairs the ability to reproduce
 * DOID:229
 * C13.351.500
 * Diseases and disorders of the female reproductive system
 * female stress incontinence
 * class of disease
 * bladder disease stress incontinence
 * Human disease
 * DOID:724
 * female urethral cancer
 * class of disease
 * urethral cancer
 * Human disease
 * DOID:738
 * female-restricted syndromic X-linked intellectual disability 99
 * class of disease
 * X-linked dominant disease X-linked intellectual disability
 * human disease
 * DOID:0112025
 * femoral cancer
 * class of disease
 * bone cancer neoplasm of femur
 * bone cancer that is located in the femur
 * DOID:5546
 * femoral neuropathy
 * class of disease
 * mononeuropathy
 * mononeuropathy that is characterized by a loss of movement or sensation in parts of the legs due to damage to the femoral nerve
 * DOID:4196
 * C10.668.829.500.200
 * femoral vein thrombophlebitis
 * class of disease
 * thrombophlebitis
 * Human disease
 * DOID:12282
 * fetal adenoma
 * class of disease
 * follicular adenoma
 * Human disease
 * DOID:8102
 * fetal akinesia deformation sequence
 * class of disease
 * Pena-Shokeir syndrome monogenic disease syndrome
 * human disease
 * DOID:0111375
 * fetal akinesia deformation sequence syndrome 1
 * class of disease
 * fetal akinesia deformation sequence autosomal recessive disease
 * human disease
 * DOID:0111377
 * fetal akinesia deformation sequence syndrome 2
 * class of disease
 * autosomal recessive disease fetal akinesia deformation sequence
 * human disease
 * DOID:0111378
 * fetal akinesia deformation sequence syndrome 3
 * class of disease
 * fetal akinesia deformation sequence autosomal recessive disease
 * human disease
 * DOID:0111376
 * fetal akinesia deformation sequence syndrome 4
 * class of disease
 * fetal akinesia deformation sequence autosomal recessive disease
 * human disease
 * DOID:0111379
 * fetal alcohol effects
 * class of disease
 * fetal alcohol spectrum disorders
 * fetal alcohol spectrum disorder that results in most, but not all, of the growth deficiency and/or craniofacial features of fetal alcohol syndrome including central nervous system dysfunction due to prenatal alcohol exposure
 * DOID:0050666
 * fetal alcohol spectrum disorders
 * class of disease
 * specific developmental disorder congenital disorder alcohol and health disease
 * group of conditions that can occur in a person whose mother drank alcohol during pregnancy
 * DOID:0050696
 * C13.703.277.220 C16.300.070 C25.775.100.087.323
 * Fetal alcohol syndrome
 * Photo of baby with FAS.jpg
 * fetal alcohol syndrome
 * class of disease
 * fetal alcohol spectrum disorders disease
 * severe form of fetal alcohol spectrum disorder
 * DOID:0050665
 * Fetal alcohol syndrome
 * FASkid.gif
 * fetal erythroblastosis
 * class of disease
 * neonatal alloimmune disease microcytic anemia hematological disease of fetus and newborn Acquired hemolytic anemia disease
 * Human disease
 * DOID:1098
 * C13.703.277.060 C15.378.295 C16.300.060 C16.614.304 C20.306
 * Hemolytic disease of the newborn
 * 1910 Erythroblastosis Fetalis.jpg
 * fetal nicotine spectrum disorder
 * class of disease
 * specific developmental disorder health effects of tobacco congenital disorder drug-induced abnormality
 * specific developmental disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of nicotine during pregnancy
 * DOID:0060606
 * Smoking and pregnancy
 * Pregnant woman smoking outside a London hospital.jpg
 * fetishism
 * class of disease
 * paraphilia fetishism disease
 * sexual arousal a person receives from an object or situation
 * DOID:1235
 * F03.657.350
 * Sexual fetishism
 * Martin van Maele - La Comtesse au fouet 01.jpg
 * fibrillary astrocytoma
 * class of disease
 * brain tumor astrocytoma diffuse astrocytoma
 * astrocytoma that is characterized as a low grade astrocytoma and has material basis in neoplastic astrocytes
 * DOID:6726
 * Fibrillary astrocytoma
 * fibroblastic liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5698
 * fibrochondrogenesis 1
 * class of disease
 * fibrochondrogenesis autosomal recessive disease
 * human disease
 * DOID:0080672
 * fibrochondrogenesis 2
 * class of disease
 * autosomal dominant disease autosomal recessive disease fibrochondrogenesis
 * human disease
 * DOID:0080673
 * fibroepithelial basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4291
 * fibroepithelial polyp of the anus
 * class of disease
 * skin tag benign neoplasm of anus polyp of rectum anal disease
 * Human disease
 * DOID:8170
 * Anal skin tags
 * fibroepithelial polyp of urethra
 * class of disease
 * skin tag urethral disease polyp urethral benign neoplasm
 * Human disease
 * DOID:8108
 * fibrogenesis imperfecta ossium
 * class of disease
 * syndrome
 * A syndrome that involves abnormality of collagen synthesis in lamellar bones, with manifestations limited to the skeleton. The initial symptom is frequently spontaneous fractures.
 * DOID:0080040
 * fibrolamellar hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma
 * A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers.
 * DOID:5015
 * fibroma
 * class of disease
 * connective tissue benign neoplasm disease
 * human disease
 * DOID:0050871
 * C04.557.450.565.590.340
 * Fibromas
 * Weiches-fibrom-augenlid.jpg
 * fibromyalgia
 * class of disease symptom or sign
 * myositis chronic pain disease
 * chronic disorder of unknown etiology characterized by pain, stiffness, and tenderness
 * DOID:631
 * C05.651.324 C05.799.321 C10.668.491.425
 * Fibromyalgia
 * Fibromyalgia pain sites APS 2019.svg
 * fibroosseous pseudotumor of digits
 * class of disease
 * bone benign neoplasm myositis ossificans
 * Human disease
 * DOID:8153
 * fibrosarcoma
 * class of disease
 * connective tissue neoplasm fibroblastic tumour sarcoma disease
 * connective tissue cancer that has material basis in fibrous connective tissue and characterized by the presence of immature proliferating fibroblasts or undifferentiated anaplastic spindle cells in a storiform pattern
 * DOID:3355
 * C04.557.450.565.590.350 C04.557.450.795.350
 * Fibrosarcoma
 * Malignant peripheral nerve sheath tumour - high mag.jpg
 * fibrosarcoma of bone
 * class of disease
 * osteosarcoma fibrosarcoma bone sarcoma
 * Human disease
 * DOID:3354
 * fibrosarcomatous osteosarcoma
 * class of disease
 * conventional central osteosarcoma
 * Human disease
 * DOID:7603
 * fibrosclerosis of breast
 * class of disease
 * non-proliferative fibrocystic change of the breast benign mammary dysplasia
 * Human disease
 * DOID:10353
 * fibrous dysplasia of bone
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that results in the destruction of normal bone and replacing it with fibrous bone tissue
 * DOID:0080031
 * C05.116.099.708.375
 * Fibrous dysplasia
 * fibrous histiocytoma
 * class of disease
 * histiocytoma
 * Human disease
 * DOID:4415
 * C04.557.450.565.590.425.350
 * fibrous meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:7211
 * fibrous synovial sarcoma
 * class of disease
 * synovial sarcoma
 * Human disease
 * DOID:5484
 * fibular collateral ligament bursitis
 * class of disease
 * knee disorder enthesopathy
 * Human disease
 * DOID:9358
 * filamentary keratitis
 * class of disease
 * keratitis
 * Human disease
 * DOID:4664
 * filarial elephantiasis
 * class of disease
 * filariasis skin disease neglected tropical disease disease
 * human disease caused by parasitic worms
 * DOID:12211
 * C15.604.496.490 C01.610.335.508.700.750.361.350 C01.920.750
 * Lymphatic filariasis
 * Elephantiasis.jpg
 * finger agnosia
 * class of disease
 * agnosia autotopagnosia
 * agnosia that is a loss of the ability to distinguish the fingers on the hand
 * DOID:0060141
 * fish allergy
 * class of disease
 * food allergy seafood allergy
 * food allergy triggered by fish
 * DOID:0060513
 * fissured tongue
 * class of disease
 * tongue disease disease
 * benign condition characterized by deep grooves (fissures) in the dorsum of the tongue
 * DOID:11514
 * C07.465.910.708
 * Fissured tongue
 * Fissured geographic tongue.jpg
 * flat ductal epithelial atypia
 * class of disease
 * breast intraductal proliferative lesion
 * Human disease
 * DOID:6841
 * flat retinoschisis
 * class of disease
 * retinoschisis
 * Human disease
 * DOID:8464
 * flavivirus infectious disease
 * class of disease
 * Flaviviridae infectious disease
 * human disease
 * DOID:993
 * C01.925.782.350.250
 * Flavivirus infections
 * focal chorioretinitis
 * class of disease
 * chorioretinitis
 * Human disease
 * DOID:1979
 * focal dystonia
 * class of disease
 * dystonia movement disorders disease
 * dystonia that is localized to a specific part of the body
 * DOID:0050836
 * focal embolic glomerulonephritis
 * class of disease
 * glomerulonephritis
 * Human disease
 * DOID:4779
 * focal epilepsy
 * class of disease
 * seizure epilepsy disease
 * epilepsy syndrome characterised by seizures preceded by isolated disturbances of a cerebral function
 * DOID:2234
 * C10.228.140.490.360
 * focal hand dystonia
 * class of disease
 * focal dystonia occupational disease
 * focal dystonia that affects a single muscle or small group of muscles in the hand resulting from involuntary muscular contractions
 * DOID:0050841
 * focal labyrinthitis
 * class of disease
 * labyrinthitis
 * Human disease
 * DOID:13867
 * focal nonepidermolytic palmoplantar keratoderma
 * class of disease
 * nonepidermolytic palmoplantar keratoderma
 * human disease
 * DOID:0111708
 * focal nonepidermolytic palmoplantar keratoderma 1
 * class of disease
 * focal nonepidermolytic palmoplantar keratoderma autosomal dominant disease
 * human disease
 * DOID:0111709
 * focal nonepidermolytic palmoplantar keratoderma 2
 * class of disease
 * autosomal dominant disease focal nonepidermolytic palmoplantar keratoderma
 * human disease
 * DOID:0111711
 * focal or diffuse nonepidermolytic palmoplantar keratoderma
 * class of disease
 * autosomal dominant disease nonepidermolytic palmoplantar keratoderma
 * human disease
 * DOID:0111710
 * focal segmental glomerulosclerosis 1
 * class of disease
 * focal segmental glomerulosclerosis genetic disease
 * A focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of ACTN4 on chromosome 19q13.2.
 * DOID:0111128
 * folic acid deficiency anemia
 * class of disease
 * deficiency anemia megaloblastic anemia nutritional deficiency disease
 * Human disease
 * DOID:14026
 * follicular adenoma
 * class of disease
 * thyroid adenoma
 * Human disease
 * DOID:6204
 * follicular basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * human disease
 * DOID:4295
 * follicular dendritic cell sarcoma
 * class of disease
 * dendritic cell sarcoma Epstein-Barr virus-associated mesenchymal tumor
 * dendritic cell sarcoma cancer that effects the follicular dendritic cells
 * DOID:6262
 * C04.557.227.190 C15.604.250.390.190
 * Follicular dendritic cell sarcoma
 * follicular mucinosis
 * class of disease
 * mucinosis alopecia sebaceous gland anomaly baldness Cutaneous focal mucinosis sebaceous gland disease
 * Human disease
 * DOID:9905
 * C17.300.550.550 C17.800.329.937.122.550 C17.800.794.550
 * follicular thyroid cancer
 * class of disease
 * thyroid carcinoma adenocarcinoma
 * thyroid carcinoma that has material basis in follicular cells
 * DOID:3962
 * C04.557.470.200.025.060
 * Follicular thyroid carcinoma
 * folliculitis
 * class of disease
 * dermatitis hair diseases disease
 * Human disease
 * DOID:4409
 * C17.800.329.500
 * Folliculitis
 * Isolated folliculitis.jpg
 * food allergy
 * class of disease
 * food hypersensitivity gastrointestinal allergy disease
 * hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body&#39;s immune system
 * DOID:3044
 * C20.543.480.370
 * Food allergy
 * Hives on back.jpg
 * form agnosia
 * class of disease
 * agnosia apperceptive agnosia visual agnosia
 * agnosia that is a loss of the ability to perceive a whole object while perceiving only parts of details
 * DOID:0060142
 * formaldehyde allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger formaldehyde
 * DOID:0040074
 * frontal convexity meningioma
 * class of disease
 * cerebral convexity meningioma
 * Human disease
 * DOID:8000
 * frontal lobe epilepsy
 * class of disease
 * extratemporal epilepsy focal epilepsy
 * common form of epilepsy that may appear to be related to a psychiatric problem or a sleep disorder
 * DOID:3331
 * C10.228.140.490.360.270 C10.228.140.490.493.188
 * frontal lobe neoplasm
 * class of disease
 * cerebrum cancer frontal lobe disorder
 * Human disease
 * DOID:12016
 * frontal sinus cancer
 * class of disease
 * paranasal sinus cancer frontal sinus neoplasm
 * Human disease
 * DOID:1360
 * frontal sinus neoplasm
 * class of disease
 * paranasal sinus neoplasm
 * Human disease
 * DOID:1361
 * frontal sinus squamous cell carcinoma
 * class of disease
 * frontal sinus cancer squamous cell carcinoma
 * Human disease
 * DOID:2441
 * frontal sinusitis
 * class of disease
 * sinusitis nose disease
 * sinusitis which involves infection of the frontal sinuses over the eyes in the brow area. This causes pain or pressure in the frontal sinus cavity and headache over the forehead
 * DOID:10791
 * C08.460.692.752.387 C08.730.749.387 C09.603.692.752.387 C01.748.749.387
 * frontometaphyseal dysplasia 1
 * class of disease
 * X-linked recessive disease frontometaphyseal dysplasia
 * human disease
 * DOID:0111786
 * frozen shoulder
 * class of disease
 * connective tissue disease periarthritis humero-scapularis capsulitis disease
 * painful human disease of uncertain origin affecting the shoulder capsule
 * DOID:14188
 * Adhesive capsulitis of the shoulder
 * Gray327.png
 * fruit allergy
 * class of disease
 * food allergy vegetable allergy
 * type of food allergy caused by fruit
 * DOID:0060503
 * functional diarrhea
 * class of disease
 * colonic disease diarrhea functional colonic disease
 * Human disease
 * DOID:11371
 * functional gastric disease
 * class of disease
 * stomach disease functional gastrointestinal disorder
 * Human disease
 * DOID:1159
 * fundus dystrophy
 * class of disease
 * eye disease retinal degeneration genetic vitreous-retinal disease
 * human disease
 * DOID:8501
 * C11.768.585.658
 * fungal esophagitis
 * class of disease
 * esophagitis fungal infectious disease
 * Human disease
 * DOID:13147
 * fungal folliculitis
 * class of disease
 * tinea corporis
 * fungal infection
 * DOID:13368
 * Fungal folliculitis
 * fungal gastritis
 * class of disease
 * gastritis fungal infectious disease chronic gastritis
 * gastrointestinal system infectious disease that involves inflammation of the stomach lining caused by fungal infection in immunocompromised patients
 * DOID:4034
 * fungal infectious disease
 * class of disease
 * infectious disease bacterial infection and mycosis disease
 * disease caused by fungi to animals or humans
 * DOID:1564
 * C01.150.703
 * Diseases and disorders due to fungi
 * Pulmonary aspergillosis.jpg
 * funisitis
 * class of disease
 * connective tissue disease chorioamnionitis
 * connective tissue disease that is an inflammation of the connective tissue of the umbilical cord
 * DOID:0050698
 * gait apraxia
 * class of disease
 * apraxia
 * Human disease
 * DOID:4260
 * C10.597.404.400 C10.597.606.881.350.600 C23.888.592.413.400 C23.888.592.604.882.350.600 F01.700.875.350.600
 * galactose epimerase deficiency
 * class of disease
 * galactosemia autosomal recessive disease
 * human disease
 * DOID:0111458
 * galactose-1-phosphate uridylyltransferase deficiency
 * class of disease
 * galactosemia autosomal recessive disease
 * human disease
 * DOID:0111459
 * gall bladder carcinoma in situ
 * class of disease
 * in situ carcinoma gallbladder disease
 * Human disease
 * DOID:0050612
 * gallamine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger gallamine
 * DOID:0040078
 * gallbladder adenocarcinoma
 * class of disease
 * gallbladder carcinoma adenocarcinoma adenocarcinoma of liver and intrahepatic biliary tract
 * gallbladder carcinoma that derives from epithelial cells of glandular origin
 * DOID:3500
 * Gallbladder adenocarcinoma
 * gallbladder adenoma
 * class of disease
 * biliary tract neoplasm gastrointestinal adenoma gallbladder polyp benign neoplasms by histologic type gallbladder benign neoplasm adenoma
 * biliary tract neoplasm that has material basis in epithelial tissue of glandular origin located in the gallbladder
 * DOID:0050893
 * gallbladder angiosarcoma
 * class of disease
 * angiosarcoma gallbladder sarcoma gallbladder cancer
 * angiosarcoma and gallbladder sarcoma that is located in the gallbladder
 * DOID:4513
 * gallbladder benign neoplasm
 * class of disease
 * gallbladder neoplasm biliary tract neoplasm
 * human disease
 * DOID:0080640
 * gallbladder cancer
 * class of disease
 * biliary tract cancer gallbladder neoplasm gallbladder disease disease
 * biliary tract cancer that is located in the gallbladder
 * DOID:3121
 * Gallbladder cancer
 * gallbladder carcinoma
 * class of disease
 * gallbladder cancer carcinoma
 * gallbladder cancer that has material basis in abnormally proliferating cells derives from epithelial cells
 * DOID:4948
 * gallbladder disease
 * class of disease
 * gastrointestinal system disease biliary disease disease
 * gastrointestinal system disease that is located in the gallbladder
 * DOID:0060262
 * C06.130.564
 * Diseases and disorders of gallbladder
 * gallbladder leiomyoma
 * class of disease
 * leiomyoma gallbladder disease gastrointestinal system benign neoplasm benign neoplasm of gallbladder
 * human disease
 * DOID:5140
 * gallbladder leiomyosarcoma
 * class of disease
 * gallbladder sarcoma leiomyosarcoma liver leiomyosarcoma gallbladder cancer
 * gallbladder sarcoma that is located in the gallbladder
 * DOID:5275
 * gallbladder lipoma
 * class of disease
 * biliary tract neoplasm gallbladder disease lipoma liver lipoma gallbladder benign neoplasm
 * human disease
 * DOID:10201
 * gallbladder lymphoma
 * class of disease
 * gallbladder cancer lymphoma liver lymphoma
 * Human disease
 * DOID:8135
 * gallbladder melanoma
 * class of disease
 * gallbladder cancer melanoma
 * Human disease
 * DOID:8167
 * gallbladder mucinous carcinoma
 * class of disease
 * gallbladder adenocarcinoma gallbladder carcinoma
 * Human disease
 * DOID:6998
 * gallbladder papillary carcinoma
 * class of disease
 * gallbladder adenocarcinoma carcinoma gallbladder cancer
 * Human disease
 * DOID:7221
 * gallbladder papillomatosis
 * class of disease
 * biliary tract neoplasm papilloma
 * Human disease
 * DOID:3120
 * gallbladder pleomorphic giant cell adenocarcinoma
 * class of disease
 * gallbladder adenocarcinoma
 * Human disease
 * DOID:7222
 * gallbladder rhabdomyosarcoma
 * class of disease
 * gallbladder sarcoma rhabdomyosarcoma liver rhabdomyosarcoma gallbladder cancer
 * gallbladder sarcoma that is located in the gallbladder
 * DOID:4057
 * gallbladder sarcoma
 * class of disease
 * gallbladder cancer sarcoma
 * sarcoma that is located in the gallbladder
 * DOID:4058
 * gallbladder signet ring cell adenocarcinoma
 * class of disease
 * gallbladder adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:3499
 * gallbladder small cell carcinoma
 * class of disease
 * gallbladder carcinoma gallbladder neuroendocrine neoplasm liver neuroendocrine carcinoma small cell carcinoma
 * Human disease
 * DOID:7133
 * gallbladder squamous cell carcinoma
 * class of disease
 * gallbladder carcinoma squamous cell carcinoma squamous cell carcinoma of liver and intrahepatic biliary tract
 * Human disease
 * DOID:5535
 * gamma heavy chain disease
 * class of disease
 * heavy chain disease
 * heavy chain disease that results from an overproduction of gamma antibody (IgG)
 * DOID:0060127
 * gamma-amino butyric acid metabolism disorder
 * class of disease
 * amino acid metabolic disorder
 * amino acid metabolic disorder characterized by impairment of the GABA catabolic pathway
 * DOID:0060176
 * gangliocytoma
 * class of disease
 * central nervous system organ benign neoplasm nervous system benign neoplasm
 * Human disease
 * DOID:2426
 * ganglioglioma
 * class of disease
 * benign neoplasms by histologic type central nervous system organ benign neoplasm
 * cell type benign neoplasm that has material basis in glial-type cells
 * DOID:5078
 * C04.557.465.625.600.380.350 C04.557.470.670.380.350 C04.557.580.625.600.380.350
 * Ganglioglioma
 * ganglioneuroblastoma
 * class of disease
 * neuroblastoma neuroblastic tumor
 * Human disease
 * DOID:4163
 * C04.557.465.625.600.590.650.550.300 C04.557.470.670.590.650.550.300 C04.557.580.625.600.590.650.550.300
 * Ganglioneuroblastoma
 * ganglioneuroma
 * class of disease
 * autonomic nervous system benign neoplasm
 * rare and benign tumor of the autonomic nerve fibers arising from neural crest sympathogonia
 * DOID:4817
 * C04.557.465.625.600.355 C04.557.470.670.355 C04.557.580.625.600.355
 * Ganglioneuroma
 * gangliosidosis
 * class of disease
 * sphingolipidosis rare genetic epilepsy rare dyslipidemia sphingolipidosis with epilepsy autosomal recessive disease disease
 * Human disease
 * DOID:2368
 * C10.228.140.163.100.435.825.300 C16.320.565.189.435.825.300 C16.320.565.398.641.803.350 C16.320.565.595.554.825.300 C18.452.132.100.435.825.300 C18.452.584.563.641.803.350 C18.452.648.189.435.825.300 C18.452.648.398.641.803.350 C18.452.648.595.554.825.300
 * gangliosidosis GM3
 * class of disease
 * gangliosidosis GM1
 * gangliosidosis that is characterized by neurodegeneration and mild skeletal changes and has material basis in mutation in the gene encoding beta-galactosidase-1
 * DOID:0080489
 * gastric adenocarcinoma
 * class of disease
 * stomach carcinoma adenocarcinoma
 * stomach carcinoma that derives from epithelial cells of glandular origin
 * DOID:3717
 * Adenocarcinomas of stomach
 * gastric adenosquamous carcinoma
 * class of disease
 * adenosquamous carcinoma gastric squamous cell carcinoma squamous cell carcinoma stomach carcinoma
 * Human disease
 * DOID:5635
 * gastric antral vascular ectasia
 * class of disease
 * capillary disease ectasia vascular ectasia
 * Human disease
 * DOID:2493
 * C06.405.748.280 C14.907.075.280
 * Gastric antral vascular ectasia
 * gastric body carcinoma
 * class of disease
 * stomach carcinoma
 * Human disease
 * DOID:6705
 * gastric cardia adenocarcinoma
 * class of disease
 * gastric adenocarcinoma gastric cardia carcinoma cardia cancer
 * Human disease
 * DOID:6271
 * gastric cardia carcinoma
 * class of disease
 * stomach carcinoma cardia cancer
 * Human disease
 * DOID:6270
 * gastric diffuse adenocarcinoma
 * class of disease
 * gastric adenocarcinoma diffuse type adenocarcinoma
 * Human disease
 * DOID:6217
 * gastric dilatation
 * class of disease
 * stomach disease
 * Human disease
 * DOID:3229
 * C06.405.748.300
 * gastric fundus cancer
 * class of disease
 * stomach cancer
 * human disease
 * DOID:10538
 * gastric fundus carcinoma
 * class of disease
 * gastric fundus cancer carcinoma
 * Human disease
 * DOID:6700
 * gastric gastrinoma
 * class of disease
 * stomach cancer gastrinoma gastric neuroendocrine tumor, well differentiated, low or intermediate grade
 * Human disease
 * DOID:5579
 * gastric hemangioma
 * class of disease
 * benign neoplasm of stomach gastrointestinal system benign neoplasm hemangioma of intra-abdominal structure hemangioma stomach disease
 * human disease
 * DOID:275
 * gastric leiomyoma
 * class of disease
 * gastrointestinal system benign neoplasm leiomyoma benign neoplasm of stomach
 * Human disease
 * DOID:10087
 * gastric leiomyosarcoma
 * class of disease
 * stomach cancer gastrointestinal system disease gastrointestinal system cancer
 * Human disease
 * DOID:5280
 * gastric liposarcoma
 * class of disease
 * stomach cancer gastrointestinal system disease gastrointestinal system cancer
 * Human disease
 * DOID:5700
 * gastric lymphoma
 * class of disease
 * gastrointestinal lymphoma stomach cancer
 * Human disease
 * DOID:10540
 * gastric mucosal hypertrophy
 * class of disease
 * gastritis rare gastroesophageal disease genetic disease rare genetic gastroenterological disease chronic gastritis
 * human disease
 * DOID:8757
 * C06.405.205.697.410 C06.405.748.398.410
 * Ménétrier's disease
 * gastric neuroendocrine neoplasm
 * class of disease
 * gastrointestinal neuroendocrine benign tumor stomach cancer
 * Human disease
 * DOID:4715
 * gastric outlet obstruction
 * class of disease
 * stomach disease
 * Human disease
 * DOID:3122
 * C06.405.748.340
 * Gastric outlet obstruction
 * gastric papillary adenocarcinoma
 * class of disease
 * gastric adenocarcinoma
 * Human disease
 * DOID:5593
 * gastric pylorus carcinoma
 * class of disease
 * stomach carcinoma pylorus cancer
 * Human disease
 * DOID:6703
 * gastric signet ring cell adenocarcinoma
 * class of disease
 * gastric diffuse adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:8025
 * gastric small cell carcinoma
 * class of disease
 * stomach carcinoma gastric neuroendocrine neoplasm small cell carcinoma
 * Human disease
 * DOID:6552
 * gastric squamous cell carcinoma
 * class of disease
 * stomach carcinoma squamous cell carcinoma
 * Human disease
 * DOID:5516
 * gastric teratoma
 * class of disease
 * stomach cancer gastrointestinal system disease gastrointestinal system cancer
 * human disease
 * DOID:5561
 * gastric tubular adenocarcinoma
 * class of disease
 * gastric adenocarcinoma
 * Human disease
 * DOID:6595
 * gastric ulcer
 * class of disease
 * peptic ulcer disease
 * An ulcerated lesion in the mucosal surface of the stomach. It may progress to involve the deeper layers of the gastric wall.
 * DOID:10808
 * C06.405.469.275.800.849 C06.405.748.586.849
 * Gastric ulcers
 * Erosive gastric ulcer.jpg
 * gastrin secretion abnormality
 * class of disease
 * endocrine pancreas disease
 * Human disease
 * DOID:13656
 * gastrinoma
 * class of disease
 * neuroendocrine tumor disease
 * neuroendocrine tumor that results in an overproduction of gastric acid
 * DOID:5577
 * C04.557.470.200.025.290.500 C04.588.274.761.500.124 C04.588.322.475.500.124 C06.301.761.500.124 C06.689.667.500.124 C19.344.421.500.124
 * Gastrinoma
 * gastritis
 * class of disease
 * stomach disease disease
 * stomach disease that is an inflammation of the lining of the stomach
 * DOID:4029
 * C06.405.205.697 C06.405.748.398
 * Gastritis
 * Gastritis erosiva.2278.jpg
 * gastroduodenal Crohn's disease
 * class of disease
 * Crohn's disease
 * inflammatory bowel disease characterized by inflammation located in stomach and located in duodenum, has symptom nausea, has symptom vomiting, has symptom weight loss and has symptom loss of appetite
 * DOID:0060191
 * gastroduodenitis
 * class of disease
 * peptic ulcer disease hemorrhagic duodenitis gastritis disease
 * Human disease
 * DOID:8644
 * gastroenteritis
 * class of disease symptom or sign
 * gastrointestinal system disease digestive sign disease
 * medical condition characterized by inflammation of the stomach and/or small intestine
 * DOID:2326
 * C06.405.205
 * Gastroenteritis
 * Gastroenteritis viruses.jpg
 * gastroesophageal adenocarcinoma
 * class of disease
 * adenocarcinoma gastroesophageal cancer
 * gastroesophageal cancer that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue
 * DOID:0080375
 * gastroesophageal cancer
 * class of disease
 * gastrointestinal system cancer
 * gastrointestinal system cancer that is located in the proximal esophagus and the distal stomach
 * DOID:0080374
 * gastroesophageal junction adenocarcinoma
 * class of disease
 * gastrointestinal carcinoma gastroesophageal adenocarcinoma
 * Human disease
 * DOID:4944
 * gastroesophageal reflux disease
 * class of disease
 * genetic disease stomach disease esophagitis gastrointestinal system disease esophageal disease
 * chronic disease caused by stomach acid coming up from the stomach into the esophagus
 * DOID:8534
 * C06.405.117.119.500.484
 * Gastroesophageal reflux disease
 * Peptic stricture.png
 * gastrointestinal adenoma
 * class of disease
 * gastrointestinal system cancer adenoma gastrointestinal system benign neoplasm
 * Human disease
 * DOID:4147
 * gastrointestinal allergy
 * class of disease
 * allergy
 * hypersensitivity reaction type I disease located in the gastrointestinal tract
 * DOID:0060502
 * gastrointestinal anthrax
 * class of disease
 * anthrax gastrointestinal system disease
 * human disease
 * DOID:13386
 * gastrointestinal carcinoma
 * class of disease
 * gastrointestinal system cancer carcinoma
 * gastrointestinal system cancer that has material basis in epithelial cells
 * DOID:0050922
 * gastrointestinal lymphoma
 * class of disease
 * gastrointestinal system cancer gastrointestinal system disease non-Hodgkin lymphoma lymphoma
 * Human disease
 * DOID:903
 * gastrointestinal neuroendocrine benign tumor
 * class of disease
 * gastrointestinal system benign neoplasm gastrointestinal system disease gastroenteropancreatic neuroendocrine neoplasm
 * Human disease
 * DOID:4148
 * gastrointestinal neuroendocrine tumor
 * class of disease
 * gastrointestinal neoplasm neuroendocrine tumor gastrointestinal system cancer
 * gastrointestinal system cancer that has material basis in neuroendocrine cells
 * DOID:0050626
 * gastrointestinal stromal tumor
 * class of disease
 * Stromal tumor rare genetic intestinal disease inherited digestive tract tumor mesenchymal tumor of small intestine gastrointestinal system cancer
 * human disease
 * DOID:9253
 * C04.557.450.565.370 C06.301.371.308 C06.405.249.308
 * Gastrointestinal stromal tumors
 * GIST 2.jpg
 * gastrointestinal system benign neoplasm
 * class of disease
 * organ system benign neoplasm gastrointestinal neoplasm gastrointestinal system disease
 * organ system benign neoplasm located in gastrointestinal tract organs
 * DOID:0050624
 * Benign neoplasms of gastrointestinal tract
 * gastrointestinal system cancer
 * class of disease
 * digestive system cancer gastrointestinal neoplasm organ system cancer gastrointestinal system disease
 * organ system cancer located in gastrointestinal tract that is manifested in organs of the gastrointestinal system
 * DOID:3119
 * Gastrointestinal cancers
 * gastrointestinal system disease
 * class of disease
 * disease of anatomical entity disease
 * disease involving the gastrointestinal tract
 * DOID:77
 * C06
 * Diseases and disorders of the digestive system
 * gastrointestinal tularemia
 * class of disease
 * tularemia gastrointestinal system disease
 * tularemia that results in formation of ulcerative lesions located in gastrointestinal tract
 * DOID:14239
 * gastrojejunal ulcer
 * class of disease
 * peptic ulcer disease
 * Human disease
 * DOID:10927
 * gastroparesis
 * class of disease
 * functional gastric disease disease
 * Human disease
 * DOID:11914
 * C06.405.748.543 C23.888.592.636.263
 * Gastroparesis
 * GastroparesisXray.jpg
 * geleophysic dysplasia 1
 * class of disease
 * geleophysic dysplasia autosomal recessive disease
 * human disease
 * DOID:0111725
 * geleophysic dysplasia 3
 * class of disease
 * geleophysic dysplasia autosomal dominant disease
 * human disease
 * DOID:0111727
 * gemistocytic astrocytoma
 * class of disease
 * astrocytoma
 * human disease
 * DOID:7005
 * Histopathology of gemistocytic astrocytoma.jpg
 * gender dysphoria
 * class of disease
 * mental disorder dysphoria disease
 * mental distress resulting from mismatch between gender identity and biological gender assigned at birth
 * DOID:1234
 * F03.835.550
 * gene duplication disease
 * class of disease
 * monogenic disease
 * human disease
 * DOID:0080712
 * generalized anxiety disorder
 * class of disease
 * anxiety disorder disease
 * anxiety disorder that is characterized by long-lasting anxiety that is not focused on any one object or situation
 * DOID:14320
 * Generalized anxiety disorder
 * generalized atherosclerosis
 * class of disease
 * atherosclerosis
 * Human disease
 * DOID:2347
 * generalized dystonia
 * class of disease
 * dystonia
 * human disease
 * DOID:0050835
 * C10.228.140.079.357 C10.228.662.300.200 C10.574.500.393 C16.320.400.330
 * generalized epidermolysis bullosa simplex
 * class of disease
 * epidermolysis bullosa simplex basal epidermolysis bullosa simplex autosomal dominant disease
 * epidermolysis bullosa simplex that is characterized by widespread blisters that appear at birth or in early infancy
 * DOID:0080511
 * generalized epilepsy
 * class of disease
 * epilepsy seizure
 * epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from independent foci or epileptic circuits that involve the whole brain
 * DOID:1827
 * C10.228.140.490.375
 * generalized epilepsy with febrile seizures plus 1
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111302
 * generalized epilepsy with febrile seizures plus 10
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111296
 * generalized epilepsy with febrile seizures plus 2
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111294
 * generalized epilepsy with febrile seizures plus 4
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111293
 * generalized epilepsy with febrile seizures plus 6
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111300
 * generalized epilepsy with febrile seizures plus 7
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111295
 * generalized epilepsy with febrile seizures plus 8
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111299
 * generalized epilepsy with febrile seizures plus 9
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111301
 * genetic disease
 * class of disease
 * hereditary disorder disease
 * health problem caused by one or more abnormalities in the genome
 * DOID:630 DOID:0050325
 * C16.320
 * Genetic diseases and disorders
 * geniculate ganglionitis
 * class of disease
 * facial nerve disease
 * Human disease
 * DOID:14075
 * geniculate herpes zoster
 * class of disease
 * herpes zoster poliomyelitis facial nerve disease
 * disorder that is caused by the reactivation of varicella zoster virus in the geniculate ganglion, a nerve cell bundle of the facial nerve
 * DOID:9210
 * C01.925.256.466.930.750.733 C07.465.299.750 C09.218.513 C10.292.319.750
 * Ramsay Hunt syndrome type II
 * genital leiomyoma
 * class of disease
 * reproductive organ benign neoplasm leiomyoma cutis
 * human disease
 * DOID:5147
 * geographic tongue
 * class of disease symptom or sign
 * inflammation tongue disease smooth tongue disease
 * atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface
 * DOID:1455
 * C07.465.910.363.447
 * Geographic tongue
 * germ cell and embryonal cancer
 * class of disease
 * germ cell cancer sarcoma
 * germ cell cancer that is derives from a mixture of germs cells and embryonal cells
 * DOID:3095
 * germ cell benign neoplasm
 * class of disease
 * benign neoplasms by histologic type germ cell tumor
 * human disease
 * DOID:0080601
 * germ cell cancer
 * class of disease
 * cell type cancer germ cell tumor
 * A cell type cancer that has_material_basis_in abnormally proliferating cells derived_from germ cells.
 * DOID:2994
 * Germ cell cancers
 * germinoma
 * class of disease
 * germ cell cancer disease
 * germ cell cancer that lacks histologic differentiation, usually a brain tumor
 * DOID:3304
 * C04.557.465.330
 * Germinoma
 * gestational choriocarcinoma
 * class of disease
 * choriocarcinoma extragonadal non-dysgerminomatous germ cell tumor extragonadal germ cell cancer gestational trophoblastic disease
 * Human disease
 * DOID:2025
 * gestational diabetes
 * class of disease
 * diabetes complication of pregnancy, childbirth and the puerperium diabetes mellitus and pregnancy disease
 * condition in which a woman without diabetes develops high blood sugar levels during pregnancy
 * DOID:11714 DOID:1550
 * C12.050.703.170 C18.452.394.750.448 C19.246.200
 * Gestational diabetes
 * Blue circle for diabetes.svg
 * gestational ovarian choriocarcinoma
 * class of disease
 * choriocarcinoma of ovary malignant non-dysgerminomatous germ cell tumor of ovary ovarian cancer gestational choriocarcinoma
 * Human disease
 * DOID:7591
 * gestational uterine corpus choriocarcinoma
 * class of disease
 * gestational choriocarcinoma uterine corpus choriocarcinoma
 * Human disease
 * DOID:8187
 * giant axonal neuropathy
 * class of disease
 * axonal neuropathy genetic disease autosomal recessive disease
 * human disease
 * DOID:0090068
 * C10.500.300.490 C10.574.500.495.490 C10.668.829.325 C10.668.829.800.300.490 C16.131.666.300.490 C16.320.400.375.490
 * giant cell glioblastoma
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by a prevalence of bizarre, multinucleated giant cells
 * DOID:3074
 * giant cell reparative granuloma
 * class of disease
 * giant-cell tumor of bone
 * Human disease
 * DOID:1866
 * C05.500.368 C07.320.391 C07.465.714.258.557 C23.550.382.468
 * giant cell tumor
 * class of disease
 * connective tissue neoplasm bone benign neoplasm
 * Human disease
 * DOID:200
 * C04.557.450.565.380
 * Giant cell tumors
 * giant hemangioma
 * class of disease
 * cavernous hemangioma
 * Human disease
 * DOID:5774
 * giant papillary conjunctivitis
 * class of disease
 * blepharoconjunctivitis papillary conjunctivitis allergic conjunctivitis
 * Human disease
 * DOID:2457
 * giant-cell carcinoma of the lung
 * class of disease
 * large-cell lung carcinoma Sarcomatoid carcinoma of the lung malignant giant cell tumor
 * lung carcinoma that is located in large undifferentiated cells
 * DOID:5583
 * C04.557.470.200.220
 * Giant cell carcinoma - Case 284 (13107156794).jpg
 * giant-cell tumor of bone
 * class of disease
 * bone neoplasm giant cell tumor disease
 * giant cell tumor and bone cancer and bone tissue neoplasm that results in the presence of multinucleated giant cells (osteoclast-like cell)
 * DOID:4305
 * C04.557.450.565.380.380 C04.557.450.565.575.420
 * Giant-cell tumor of bone
 * Giant cell tumour of bone - high mag.jpg
 * gingival disease
 * class of disease
 * periodontal disease
 * human disease
 * DOID:1483
 * C07.465.714.258
 * gingival fibromatosis 5
 * class of disease
 * gingival fibromatosis autosomal dominant disease
 * human disease
 * DOID:0080280
 * gingival hypertrophy
 * class of disease
 * gingival overgrowth
 * Human disease
 * DOID:5338
 * C07.465.714.258.428.260
 * gingival overgrowth
 * class of disease
 * gingival disease
 * Human disease
 * DOID:3086
 * C07.465.714.258.428
 * Gingival enlargement
 * gingival recession
 * class of disease
 * gingival disease periodontal atrophy
 * human disease
 * DOID:1134
 * C07.465.714.258.447 C07.465.714.354.625
 * Gingival recession
 * gingivitis
 * class of disease symptom or sign
 * symptom gingival disease periodontitis disease
 * inflammation of the gums
 * DOID:3087
 * C07.465.714.258.480
 * Gingivitis
 * Gingivitis (crop).jpg
 * glandular cystitis
 * class of disease
 * chronic cystitis
 * A reactive inflammatory disorder affecting the bladder. It is characterized by the development of small cysts in the bladder wall. The cysts are lined by metaplastic glandular cells.
 * DOID:2392
 * Cystitis glandularis
 * glandular pattern ovarian yolk sac tumor
 * class of disease
 * ovarian endodermal sinus tumor
 * Human disease
 * DOID:6511
 * glandular tularemia
 * class of disease
 * tularemia
 * tularemia that results in swelling of regional lymph glands
 * DOID:0050382
 * glandular-alveolar pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:7930
 * glans penis cancer
 * class of disease
 * penile cancer
 * Human disease
 * DOID:11839
 * glassy cell variant cervical adenosquamous carcinoma
 * class of disease
 * cervical adenosquamous carcinoma
 * cervical adenosquamous carcinoma that is a rare form and is composed of cells with a glass-like cytoplasm
 * DOID:8361
 * glaucoma
 * class of disease
 * eye disease disease
 * eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function
 * DOID:1686
 * C11.525.381
 * Glaucoma
 * Acute Angle Closure-glaucoma.jpg
 * glaucomatous atrophy of optic disc
 * class of disease
 * optic atrophy eye degenerative disease
 * human disease
 * DOID:10337
 * glioblastoma
 * class of disease
 * astrocytoma disease
 * human disease
 * DOID:3068
 * C04.557.465.625.600.380.080.335 C04.557.470.670.380.080.335 C04.557.580.625.600.380.080.335
 * Glioblastoma
 * Glioblastoma (1).jpg
 * glioblastoma classical subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by abnormally high levels of epidermal growth factor receptor and the absence of p53 mutations
 * DOID:0050803
 * glioblastoma mesenchymal subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by the most frequent number of mutation of the Neurofibromin 1 gene
 * DOID:0050805
 * glioblastoma neural subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by the expression of several gene types that are also typical of the brain&#39;s normal, noncancerous nerve cells, or neurons
 * DOID:0050806
 * glioblastoma proneural subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by IDH1 and p53 mutations and Platelet Derived Growth Factor A amplification
 * DOID:0050804
 * glioma
 * class of disease
 * cell type cancer brain tumor spinal disease bone cancer brain cancer disease
 * type of tumor that starts in the brain or spine
 * DOID:3070
 * C04.557.465.625.600.380 C04.557.470.670.380 C04.557.580.625.600.380
 * Gliomas
 * Glioma.gif
 * gliomatosis cerebri
 * class of disease
 * brain cancer
 * rare primary brain tumor
 * DOID:6128
 * Gliomatosis cerebri
 * Gliomatosis cerebri.jpg
 * gliosarcoma
 * class of disease
 * glioblastoma
 * Human disease
 * DOID:3071
 * C04.557.465.625.600.380.400 C04.557.470.670.380.400 C04.557.580.625.600.380.400
 * Gliosarcoma
 * globe disease
 * class of disease
 * eye disease
 * Human disease
 * DOID:1242
 * globoszoospermia
 * class of disease
 * Teratospermia male infertility autosomal recessive disease spermatogenic failure
 * male infertility characterized by round-headed spermatozoa lacking an acrosome
 * DOID:0111156
 * Globoszoospermia
 * Globozoospermia.png
 * glomangioma
 * class of disease
 * benign perivascular tumor glomus tumor
 * Human disease
 * DOID:2436
 * glomangiomatosis
 * class of disease
 * benign perivascular tumor glomus tumor
 * Human disease
 * DOID:6906
 * glomangiomyoma
 * class of disease
 * benign perivascular tumor glomus tumor
 * human disease
 * DOID:8020
 * glomangiosarcoma
 * class of disease
 * glomus tumor
 * Human disease
 * DOID:5233
 * glomeruloid hemangioma
 * class of disease
 * hemangioma
 * Human disease
 * DOID:486
 * glomerulonephritis
 * class of disease symptom or sign
 * nephritis glomerulopathy disease
 * nephritis that causes inflammation of the glomeruli located in kidney
 * DOID:2921
 * C12.777.419.570.363 C13.351.968.419.570.363
 * Glomerulonephritis
 * Crescentic glomerulonephritis HE stain.JPEG
 * glomerulosclerosis
 * class of disease
 * glomerulonephritis
 * glomerulonephritis that is characterized by hardening of the glomerulus in the kidney
 * DOID:0050851
 * Glomerulosclerosis
 * glossitis
 * class of disease symptom or sign
 * tongue disease inflammatory disease disease
 * soreness of the tongue, or more usually inflammation with depapillation of the dorsal surface of the tongue
 * DOID:1456
 * C07.465.910.363
 * Glossitis
 * Scharlach.JPG
 * glossopharyngeal motor neuropathy
 * class of disease
 * motor neuritis glossopharyngeal nerve disease
 * Human disease
 * DOID:7558
 * glossopharyngeal nerve disease
 * class of disease
 * cranial nerve disease
 * Human disease
 * DOID:3418
 * C10.292.450
 * glossopharyngeal nerve paralysis
 * class of disease
 * glossopharyngeal nerve disease cranial nerve palsy
 * Human disease
 * DOID:3816
 * glossopharyngeal neuralgia
 * class of disease
 * glossopharyngeal nerve disease neuralgia cranial neuralgia
 * Human disease
 * DOID:14423
 * glottis cancer
 * class of disease
 * laryngeal cancer glottis neoplasm
 * Human disease
 * DOID:2595
 * glottis carcinoma
 * class of disease
 * glottis cancer carcinoma
 * Human disease
 * DOID:2599
 * glottis neoplasm
 * class of disease
 * laryngeal neoplasm
 * Human disease
 * DOID:2597
 * glucocorticoid deficiency 1
 * class of disease
 * familial glucocorticoid deficiency autosomal recessive disease
 * human disease
 * DOID:0080621
 * glucocorticoid-induced osteoporosis
 * class of disease
 * corticosteroid-induced osteoporosis osteoporosis
 * Human disease
 * DOID:0060343
 * glucose intolerance
 * class of disease
 * hyperglycemia disease
 * pre-diabetic state of hyperglycemia that is associated with insulin resistance and increased risk of cardiovascular pathology. IGT may precede type 2 diabetes mellitus by many years
 * DOID:10603
 * C18.452.394.952.500
 * glucose metabolism disease
 * class of disease
 * carbohydrate metabolism disease metabolic disease
 * metabolic disorder characterized by abnormal blood glucose levels
 * DOID:4194
 * C18.452.394
 * Glucose metabolism disorders
 * glucose-6-phosphate dehydrogenase deficiency
 * class of disease
 * carbohydrate metabolic disorder disease
 * carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH)
 * DOID:2862
 * C15.378.071.141.150.480 C16.320.070.480 C16.320.565.202.402 C18.452.648.202.402
 * Glucose-6-phosphate dehydrogenase deficiency
 * G6PD - 3D structure - PDB1qki.png
 * glutathionuria
 * class of disease
 * Congenital disorders of amino acid metabolism inborn disorder of the gamma-glutamyl cycle amino acid metabolic disorder autosomal recessive disease
 * Gamma-glutamyl transpeptidase deficiency is characterized by increased glutathione concentration in the plasma and urine
 * DOID:0111257
 * gluten allergy
 * class of disease
 * food allergy gluten-related disorder
 * allergy involving gluten
 * DOID:0060057
 * glycogen metabolism disorder
 * class of disease
 * carbohydrate metabolic disorder
 * carbohydrate metabolism disorder that is characterized by abnormal accumulation or depletion of liver glycogen
 * DOID:0050728
 * glycogen storage disease
 * class of disease
 * glycogen metabolism disorder overload disease carbohydrate metabolic disorder disease
 * glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types
 * DOID:2747
 * C16.320.565.202.449 C18.452.648.202.449
 * Glycogen storage disease
 * Glycogen storage disorder (PAS with diastase).jpg
 * glycogen storage disease IX
 * class of disease
 * glycogen storage disease
 * glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity
 * DOID:0050594
 * Glycogen storage disease type IX
 * glycogen-rich clear cell breast carcinoma
 * class of disease
 * breast adenocarcinoma clear cell carcinoma
 * Human disease
 * DOID:5310
 * goat milk allergy
 * class of disease
 * milk allergy
 * milk allergy triggered by Capra hircus milk
 * DOID:0060522
 * goiter
 * class of disease
 * thyroid gland disease disease
 * swelling of the thyroid gland
 * DOID:12176
 * C19.874.283
 * Goiters
 * Kone med stor struma.jpg
 * gonadal disease
 * class of disease
 * endocrine system disease
 * endocrine system disease that is located in the gonads
 * DOID:2277
 * C19.391
 * Diseases and disorders of gonads
 * gonadal dysgenesis
 * class of disease
 * hypogonadism sex differentiation disease disease
 * congenital disorder of the reproductive system
 * DOID:14447
 * C12.706.316.309 C13.351.875.253.309 C16.131.939.316.309 C19.391.119.309
 * gonadoblastoma
 * class of disease
 * benign neoplasms by histologic type
 * cell type benign neoplasm that is composed of a mixture of gonadal elements
 * DOID:3301
 * C04.557.465.420 C04.557.475.395 C12.706.316.096.687.500 C12.706.316.309.388.500 C13.351.875.253.096.687.500 C13.351.875.253.309.388.500 C16.131.939.316.096.687.500 C16.131.939.316.309.388.500 C19.391.119.096.687.500 C19.391.119.309.388.500
 * Gonadoblastoma
 * gonococcal bursitis
 * class of disease
 * bursitis gonococcal infectious diseases
 * Human disease
 * DOID:13453
 * gonococcal seminal vesiculitis
 * class of disease
 * vesiculitis gonorrhea
 * human disease
 * DOID:10400
 * gonococcal spondylitis
 * class of disease
 * spondylitis gonorrhea
 * Human disease
 * DOID:13127
 * gonococcal synovitis
 * class of disease
 * synovitis gonococcal infectious diseases
 * Human disease
 * DOID:13454
 * gout
 * class of disease symptom or sign
 * arthritis genetic disease crystal arthropathy metabolic disease disease
 * medical condition that results in recurrent pain and swelling of joints
 * DOID:13189
 * C05.550.114.423 C05.550.354.500 C05.799.414 C16.320.565.798.368 C18.452.648.798.368
 * Gout
 * Gout2010.JPG
 * granular cell carcinoma
 * class of disease
 * carcinoma
 * carcinoma that derives from epithelial cells, with polygonal accumulation of secondary lysosomes in the cytoplasm
 * DOID:4903
 * granular cell leiomyosarcoma
 * class of disease
 * leiomyosarcoma rare nervous system tumor malignant granular cell myoblastoma
 * Human disease
 * DOID:5258
 * granular cell tumor
 * class of disease
 * skin benign neoplasm
 * Human disease
 * DOID:2411
 * C04.557.450.590.350
 * Granular cell tumor
 * Granular cell tumor Case 174 (5600864519).jpg
 * granuloma annulare
 * class of disease
 * dermatitis necrobiotic disorders
 * Human disease
 * DOID:3777
 * C17.300.200.495.380 C17.800.550.380 C23.550.382.375
 * Granuloma annulare
 * Granuloma annulare.jpg
 * granulomatous amebic encephalitis
 * class of disease
 * Balamuthia infection acanthamoebiasis primary amebic meningoencephalitis encephalopathy
 * Human disease
 * DOID:0050246
 * Granulomatous amoebic encephalitis
 * granulomatous angiitis
 * class of disease
 * vasculitis central nervous system vasculitis
 * Human disease
 * DOID:2555
 * granulomatous dermatitis
 * class of disease
 * dermatitis
 * Human disease
 * DOID:4397
 * granulomatous endometritis
 * class of disease
 * endometritis chronic endometritis
 * Human disease
 * DOID:4561
 * granulomatous gastritis
 * class of disease
 * gastritis chronic gastritis
 * Human disease
 * DOID:4038
 * granulomatous hepatitis
 * class of disease
 * hepatitis hepatic granuloma
 * Human disease
 * DOID:2239
 * granulomatous myositis
 * class of disease
 * myositis
 * Human disease
 * DOID:3428
 * granulomatous orchitis
 * class of disease
 * testicular disease
 * Human disease
 * DOID:3089
 * granulosa cell tumour
 * class of disease
 * ovarian cancer sex cord-gonadal stromal tumor
 * Human disease
 * DOID:2999
 * C04.557.475.750.656 C04.588.322.455.398 C13.351.500.056.630.705.398 C13.351.937.418.685.398 C19.344.410.398 C19.391.630.705.398
 * Granulosa cell tumors
 * gray zone lymphoma
 * class of disease
 * lymphoma
 * lymphoma that is characterized by having cellular features of both classic Hodgkin&#39;s lymphomas and large B-cell Lymphomas
 * DOID:5822
 * green color blindness
 * class of disease
 * dichromatopsia deuteranopia
 * human disease
 * DOID:13909
 * green mud crab allergy
 * class of disease
 * crustacean allergy
 * crustacean allergy triggered by Scylla paramamosain
 * DOID:0060526
 * growth hormone insensitivity syndrome with immune dysregulation 2
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0080837
 * growth hormone secreting pituitary adenoma 2
 * class of disease
 * growth hormone secreting pituitary adenoma
 * human disease
 * DOID:0112007
 * gynatresia
 * class of disease
 * female reproductive system disease atresia
 * Human disease
 * DOID:429
 * C13.351.500.320
 * gynecomastia
 * class of disease
 * sex differentiation disease
 * human disorder, which causes the appearance of breasts in males
 * DOID:12698
 * C17.800.090.875
 * Gynecomastia
 * gyrate atrophy of the choroid
 * class of disease
 * disease choroid disease central gyrate choroidal dystrophy
 * Human disease
 * DOID:1415
 * C11.270.468 C11.941.160.578 C16.320.290.468
 * haemophilus meningitis
 * class of disease
 * bacterial meningitis Haemophilus influenzae infectious disease
 * bacterial meningitis that has material basis in Haemophilus influenzae infection
 * DOID:0080179
 * C01.150.252.223.500.425 C01.150.252.400.700.433.615 C10.228.228.180.500.425 C10.586.625.280.393 C01.207.180.500.425
 * hair diseases
 * class of disease
 * integumentary system disease
 * integumentary system disease that is located in hair
 * DOID:421
 * C17.800.329
 * hair follicle neoplasm
 * class of disease
 * skin benign neoplasm hair diseases
 * skin tumor derived from the hair matrix
 * DOID:5375
 * hairy cell leukemia
 * class of disease
 * chronic lymphocytic leukemia B-cell leukemia disease
 * chronic lymphocytic leukemia that is characterized by over production of B cells (lymphocytes) by the bone marrow where the B cells appear hairy under a microscope
 * DOID:285
 * C04.557.337.415 C15.604.515.553 C20.683.515.517
 * Hairy cell leukemia
 * hairy tongue
 * class of disease
 * tongue disease disease
 * Human disease
 * DOID:13500
 * C07.465.910.791
 * Black hairy tongue
 * Black tongue.jpg
 * hallucinogen abuse
 * class of disease
 * substance abuse
 * substance abuse that involves the recurring use of hallucinogenic drugs despite negative consequences
 * DOID:12797
 * hallucinogen dependence
 * class of disease
 * substance dependence hallucinogen abuse
 * drug dependence that involves the continued use of hallucinogenic drugs despite problems related to use of the substance
 * DOID:9977
 * hand dermatosis
 * class of disease
 * skin disease
 * disease class
 * DOID:3158
 * C17.800.338
 * head and neck cancer
 * class of disease
 * organ system cancer head and neck neoplasms respiratory system cancer disease
 * organ system cancer in the head or neck region
 * DOID:11934 DOID:3680
 * Head and neck cancer
 * PET-CT scanning of lymph node metastases in cancer 2.jpg
 * head and neck carcinoma
 * class of disease
 * head and neck cancer carcinoma
 * human disease
 * DOID:1542
 * heart cancer
 * class of disease
 * cardiovascular cancer Primary tumors of the heart heart disease thoracic cancer
 * cardiovascular cancer located in the heart
 * DOID:117
 * Heart cancer
 * Myxoma.jpg
 * heart disease
 * class of disease
 * cardiovascular disease
 * cardiovascular system disease that involves the heart
 * DOID:114
 * C14.280
 * Diseases and disorders of the heart
 * heart fibrosarcoma
 * class of disease
 * heart sarcoma fibrosarcoma
 * Human disease
 * DOID:6033
 * heart leiomyosarcoma
 * class of disease
 * heart sarcoma
 * Human disease
 * DOID:5261
 * heart lipoma
 * class of disease
 * cardiovascular organ benign neoplasm Primary tumors of the heart heart disease benign neoplasm of heart lipoma
 * Human disease
 * DOID:6285
 * heart lymphoma
 * class of disease
 * heart cancer lymphoma
 * Human disease
 * DOID:6547
 * heart malignant hemangiopericytoma
 * class of disease
 * heart sarcoma hemangiopericytoma
 * heart sarcoma that is a soft tissue sarcoma located in the heart
 * DOID:6034
 * heart sarcoma
 * class of disease
 * heart cancer
 * sarcoma and malignant neoplasm of heart that is located in the heart
 * DOID:5262
 * heart septal defect
 * class of disease
 * congenital heart disease
 * Human disease
 * DOID:1681
 * C14.240.400.560 C14.280.400.560 C16.131.240.400.560
 * Heart septal defects
 * heart valve disease
 * class of disease
 * heart disease disease
 * disease in the valves of the heart
 * DOID:4079
 * C14.280.484
 * Diseases and disorders of the heart valves
 * heavy chain disease
 * class of disease
 * type IV hypersensitivity
 * hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains
 * DOID:0060125
 * C15.378.147.780.490 C15.604.515.435 C20.683.780.490
 * hemangioblastoma
 * class of disease
 * hemangioma rare nervous system tumor disease
 * tumor of the central nervous system that originates from the vascular system
 * DOID:5241
 * C04.557.645.375.380.370
 * Hemangioblastomas
 * Hemangioblastoma cerebellum.jpg
 * hemangioma
 * class of disease
 * angioma vascular neoplasm cardiovascular organ benign neoplasm benign neoplasms by histologic type vascular disease disease
 * cell type benign neoplasm that has physical basis in endothelial cells that line blood vessels
 * DOID:255
 * C04.557.645.375
 * Skin hemangioma
 * Capillary haemangioma.jpg
 * hemangioma of intra-abdominal structure
 * class of disease
 * hemangioma
 * Human disease
 * DOID:254
 * hemangioma of lung
 * class of disease
 * hemangioma lung benign neoplasm
 * human disease
 * DOID:490
 * hemangioma of orbit
 * class of disease
 * orbital disease hemangioma
 * Human disease
 * DOID:14459
 * hemangioma of peripheral nerve
 * class of disease
 * hemangioma peripheral nervous system benign neoplasm peripheral neuropathy
 * Human disease
 * DOID:482
 * hemangioma of spleen
 * class of disease
 * splenic disease hemangioma of intra-abdominal structure
 * Human disease
 * DOID:256
 * hemangioma of subcutaneous tissue
 * class of disease
 * skin hemangioma subcutaneous tissue disease vascular skin disease skin benign neoplasm hemangioma
 * Human disease
 * DOID:13081
 * hemangiopericytic tumor
 * class of disease
 * perivascular tumor
 * Human disease
 * DOID:3850
 * hemangiopericytoma
 * class of disease
 * connective tissue neoplasm hemangiopericytic tumor
 * soft tissue cancer that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries
 * DOID:264
 * C04.557.645.380
 * Haemangiopericytoma
 * hematocele of tunica vaginalis testis
 * class of disease symptom or sign
 * testicular disease hematocele
 * Human disease
 * DOID:12332
 * C12.294.287 C23.550.414.817
 * Hematocele
 * hematologic cancer
 * class of disease symptom or sign
 * organ system cancer hematopoietic system disease tumor of hematopoietic and lymphoid tissues
 * immune system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes
 * DOID:2531
 * Cancers of the lymph nodes and haematopoiesis
 * hematopoietic system disease
 * class of disease
 * symptom disease of anatomical entity
 * disorder which primarily affects the blood
 * DOID:74
 * C15.378
 * Diseases and disorders of the blood
 * hemidystonia
 * class of disease
 * multifocal dystonia
 * multifocal dystonia that involves the arm and leg on the same side of the body
 * DOID:0050846
 * hemiparesis
 * class of disease symptom or sign
 * paresis paralysis central nervous system disease disease
 * weakness of one side of the body
 * DOID:10969
 * hemochromatosis type 1
 * class of disease
 * HFE hereditary haemochromatosis genetic disease
 * hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22
 * DOID:0111029
 * hemochromatosis type 2
 * class of disease
 * iron overload HFE hereditary haemochromatosis
 * hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis
 * DOID:0111034
 * hemochromatosis type 2B
 * class of disease
 * hemochromatosis type 2 genetic disease
 * hemochromatosis type 2 that has material basis in homozygous mutation in the HAMP gene on chromosome 19q13
 * DOID:0111032
 * hemoglobin C
 * class of disease
 * hemoglobinopathy congenital hemolytic anemia disease
 * Human disease
 * DOID:2859
 * C15.378.071.141.150.490 C15.378.420.463 C16.320.070.490 C16.320.365.463
 * hemoglobin D disease
 * class of disease
 * hemoglobinopathy congenital hemolytic anemia
 * Human disease
 * DOID:5378
 * hemoglobin E
 * class of disease
 * hemoglobinopathy congenital hemolytic anemia
 * variant form of human hemoglobin
 * DOID:5379
 * D12.776.124.400.463.375 D12.776.422.316.762.426.375
 * hemoglobin H disease
 * class of disease
 * alpha thalassemia
 * alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other
 * DOID:0110031
 * hemoglobinopathy
 * class of disease
 * congenital hemolytic anemia genetic disease hemolytic anemia hemoglobin variant disease
 * genetic defect causing abnormal hemoglobin structure
 * DOID:2860
 * C15.378.420 C16.320.365
 * hemoglobinuria
 * class of disease
 * proteinuria hemolytic anemia disease
 * condition in which the oxygen transport protein hemoglobin is found in abnormally high concentrations in the urine
 * DOID:582
 * C12.777.934.734.634 C13.351.968.934.734.634 C23.888.942.750.634
 * 1GZX Haemoglobin.png
 * hemolytic-uremic syndrome
 * class of disease
 * kidney disease disease
 * Human disease
 * DOID:12554
 * C12.050.351.968.419.936.463 C12.200.777.419.936.463 C15.378.071.141.610 C15.378.140.855.925.500 C12.950.419.936.463 C15.378.243.937.925.500
 * Hemolytic-uremic syndrome
 * Schizocyte smear 2009-12-22.JPG
 * hemometra
 * class of disease
 * uterine disease menstrual disorder disease
 * Human disease
 * DOID:9958
 * C13.351.500.852.495
 * Hematometra
 * hemopericardium
 * class of disease
 * pericardial effusion
 * pericardial effusion that results from blood in the pericardial sac
 * DOID:11482
 * Hemopericardium
 * hemophagocytic lymphohistiocytosis
 * class of disease
 * lymphatic system disease disease
 * uncommon hematologic disorder seen more often in children than in adults
 * DOID:0050120
 * C15.604.250.410.575
 * Hemophagocytic lymphohistiocytosis
 * Hemophagocytic syndrome - cropped - very high mag.jpg
 * hemophilia A
 * class of disease symptom or sign
 * hemophilia coagulation factor deficiency X-linked recessive disease blood coagulation disease disease
 * X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged
 * DOID:12134
 * C15.378.100.100.500 C15.378.100.141.500 C15.378.463.500 C16.320.099.500
 * Hemophilia A
 * hemophilia B
 * class of disease
 * coagulation factor deficiency inherited blood coagulation disease X-linked recessive disease blood coagulation disease disease
 * An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
 * DOID:12259
 * C15.378.100.100.510 C15.378.100.141.510 C15.378.463.510 C16.320.099.510 C16.320.322.235
 * Hemophilia B
 * hemopneumothorax
 * class of disease
 * pneumothorax hemothorax disease
 * medical term describing the combination of two conditions: pneumothorax, or air in the chest cavity, and hemothorax (also called hæmothorax), or blood in the chest cavity
 * DOID:2718
 * C08.528.338 C23.550.414.904.500
 * hemorrhagic cystitis
 * class of disease
 * cystitis
 * Inflammation of the bladder resulting in bloody urine
 * DOID:0050859
 * C12.050.351.968.829.495.250 C12.200.777.829.495.250 C12.950.829.495.250
 * hemorrhagic disease
 * class of disease
 * blood coagulation disease disease
 * human disease
 * DOID:2213
 * C15.378.463
 * hemorrhoid
 * class of disease
 * gastrointestinal system disease pelvic varices anorectal disorder anal disease skin disease disease
 * vascular structures in the anal canal
 * DOID:9746
 * C06.405.469.860.401 C14.907.449
 * Hemorrhoids
 * Hemorrhoid.png
 * hemosiderosis
 * class of disease
 * iron overload iron metabolism disease disease
 * iron metabolism disease that has material basis in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload
 * DOID:12119
 * C18.452.565.500.500
 * Hemosiderosis
 * Hemosiderin1.jpg
 * hepatic angiomyolipoma
 * class of disease
 * liver neoplasm
 * Human disease
 * DOID:3317
 * hepatic flexure cancer
 * class of disease
 * ascending colon cancer
 * Human disease
 * DOID:260
 * hepatic hemangioma
 * class of disease
 * liver neoplasm hemangioma of intra-abdominal structure hemangioma hepatic vascular disease
 * non-cancerous tumor of the liver
 * DOID:271
 * Liver hemangioma
 * hepatic infarction
 * class of disease
 * hepatic vascular disease infarction ischemic hepatitis
 * Human disease
 * DOID:13738
 * C06.552.289 C23.550.513.355.500 C23.550.717.489.500
 * Hepatic infarction
 * hepatic osteogenic sarcoma
 * class of disease
 * extraosseous osteosarcoma liver cancer
 * Human disease
 * DOID:6370
 * hepatic vascular disease
 * class of disease
 * vascular disease liver disease
 * vascular disease that is located in the liver
 * DOID:272
 * hepatic veno-occlusive disease
 * class of disease
 * hepatic vascular disease vein disorder
 * hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver
 * DOID:0080177
 * C06.552.360 C14.907.460
 * hepatitis
 * class of disease symptom or sign
 * liver disease inflammation liver symptom disease
 * inflammation of the liver tissue
 * DOID:2237
 * C06.552.380
 * Hepatitis
 * Alcoholic hepatitis.jpg
 * hepatobiliary neoplasm
 * class of disease
 * gastrointestinal system benign neoplasm liver and intrahepatic bile duct neoplasm
 * gastrointestinal system neoplasm located in the hepatobiliary system
 * DOID:3117
 * hepatobiliary system cancer
 * class of disease
 * gastrointestinal system cancer liver and intrahepatic bile duct neoplasm
 * gastrointestinal system cancer that is located in the hepatobiliary system
 * DOID:0080355
 * hepatoblastoma
 * class of disease
 * liver cancer disease
 * uncommon malignant liver cancer occurring in infants and children
 * DOID:687
 * C04.557.435.380
 * Hepatoblastoma
 * Hepatoblastoma.jpg
 * hepatocellular adenoma
 * class of disease
 * liver neoplasm endocrine gland cancer benign neoplasms by histologic type adenoma disease
 * Hepatocellular adenoma (HA) is a rare benign tumor of the liver
 * DOID:0050868
 * C04.557.470.035.120 C04.588.274.623.040 C06.301.623.040 C06.552.697.040
 * Hepatic adenoma
 * Hepatic adenoma low mag.jpg
 * hepatocellular carcinoma
 * class of disease
 * liver carcinoma disease
 * liver carcinoma that has material basis in undifferentiated hepatocytes
 * DOID:684
 * C04.557.470.200.025.255 C04.588.274.623.160 C06.301.623.160 C06.552.697.160
 * Hepatocellular carcinoma
 * Hepatocellular carcinoma 1.jpg
 * hepatocellular clear cell carcinoma
 * class of disease
 * hepatocellular carcinoma clear cell carcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5016
 * hepatoid adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver
 * DOID:0060534
 * hepatoid pattern ovarian yolk sac tumor
 * class of disease
 * ovarian endodermal sinus tumor
 * Human disease
 * DOID:6512
 * hepatoid pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8195
 * hepatopulmonary syndrome
 * class of disease
 * liver disease
 * Human disease
 * DOID:900
 * C06.552.455 C08.381.385
 * hepatorenal syndrome
 * class of disease
 * acute kidney injury disease
 * Human disease
 * DOID:11823
 * C06.552.465 C12.777.419.291 C13.351.968.419.291
 * Hepatorenal syndrome
 * hereditary ataxia
 * class of disease
 * neurodegeneration
 * neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements
 * DOID:0050951
 * hereditary Wilms' tumor
 * class of disease
 * nephroblastoma inherited renal tumor
 * nephroblastoma that results in either bilateral disease or a family history of Wilms&#39; tumour
 * DOID:5183
 * hereditary alpha tryptasemia syndrome
 * class of disease
 * gene duplication disease syndrome
 * DOID:0080714
 * hereditary angioedema
 * class of disease symptom or sign
 * angioedema disease
 * Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain
 * DOID:14735
 * C14.907.079.500 C16.320.798.500.500 C17.800.862.945.066.500 C20.543.480.904.066.500 C20.673.795.500.500
 * Hereditary angioedema
 * Gezichtsoedeem.jpg
 * hereditary breast ovarian cancer
 * class of disease
 * autosomal dominant disease hereditary neoplastic syndromes syndrome disease
 * autosomal dominant disease characterized by the higher than normal tendency to develop breast and ovarian cancers in genetically related families
 * DOID:5683
 * C04.588.180.483 C04.588.322.455.431 C04.700.517 C13.351.500.056.630.705.431 C13.351.937.418.685.431 C16.320.700.517 C17.800.090.500.483 C19.344.410.431 C19.391.630.705.431
 * hereditary choroidal atrophy
 * class of disease
 * choroidal sclerosis
 * human disease
 * DOID:9794
 * hereditary combined deficiency of vitamin K-dependent clotting factors
 * class of disease
 * monogenic disease blood coagulation disease
 * human disease
 * DOID:0112172
 * hereditary conventional renal cell carcinoma
 * class of disease
 * hereditary renal cell carcinoma renal clear cell carcinoma
 * Human disease
 * DOID:7192
 * hereditary diffuse gastric cancer
 * class of disease
 * hereditary gastric cancer stomach cancer autosomal dominant disease diffuse gastric cancer
 * medical condition
 * DOID:0080764
 * hereditary lymphedema
 * class of disease
 * lymphedema Primary lymphedema disease
 * lymphedema commonly located in legs, caused by congenital abnormalities in the lymphatic system
 * DOID:0050580
 * hereditary lymphedema I
 * class of disease
 * hereditary lymphedema
 * hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood
 * DOID:0070212
 * hereditary lymphedema IA
 * class of disease
 * hereditary lymphedema genetic disease autosomal dominant disease
 * hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the FLT4 gene on chromosome 5q35
 * DOID:0070210
 * hereditary lymphedema IB
 * class of disease
 * hereditary lymphedema autosomal dominant disease
 * A hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in the chromosomal region 6q16.2-q22.1.
 * DOID:0070211
 * hereditary lymphedema IC
 * class of disease
 * hereditary lymphedema genetic disease autosomal dominant disease
 * hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the GJC2 gene on chromosome 1q42
 * DOID:0070208
 * hereditary lymphedema ID
 * class of disease
 * hereditary lymphedema genetic disease autosomal dominant disease
 * hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the VEGFC gene on chromosome 4q34
 * DOID:0070209
 * hereditary lymphedema II
 * class of disease
 * hereditary lymphedema autosomal dominant disease
 * hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance
 * DOID:0070213
 * hereditary mixed polyposis syndrome 1
 * class of disease
 * hereditary mixed polyposis syndrome chromosomal duplication syndrome
 * human disease
 * DOID:0111685
 * hereditary motor and sensory neuropathy
 * class of disease
 * congenital disorder Sensorimotor neuropathy peripheral neuropathy hereditary peripheral neuropathy
 * congenital disorder of nervous system
 * DOID:2477
 * C10.500.300 C10.574.500.495 C10.668.829.800.300 C16.131.666.300 C16.320.400.375
 * Hereditary motor and sensory neuropathies
 * hereditary neutrophilia
 * class of disease
 * leukocyte disease neutrophilia rare genetic immune disease genetic hematologic disease genetic disease autosomal dominant disease
 * human disease
 * DOID:0090120
 * hereditary night blindness
 * class of disease
 * night blindness
 * Human disease
 * DOID:8498
 * hereditary nonpolyposis colorectal cancer type 2
 * class of disease
 * Lynch syndrome
 * A Lynch syndrome that has material basis in mutations in the MLH1 gene on chromosome 3p22.2.
 * DOID:0070274
 * hereditary nonpolyposis colorectal cancer type 4
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutation in the PMS2 gene on chromosome 7p22
 * DOID:0070275
 * hereditary nonpolyposis colorectal cancer type 5
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutation in the MSH6 gene on chromosome 2p16
 * DOID:0070272
 * hereditary nonpolyposis colorectal cancer type 6
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p22
 * DOID:0070273
 * hereditary nonpolyposis colorectal cancer type 7
 * class of disease
 * Lynch syndrome
 * A Lynch syndrome that has material basis in mutation in the MLH3 gene on chromosome 14q24.3.
 * DOID:0070276
 * hereditary nonpolyposis colorectal cancer type 8
 * class of disease
 * Lynch syndrome chromosomal deletion syndrome
 * human disease
 * DOID:0070270
 * hereditary papulotranslucent acrokeratoderma
 * class of disease
 * cholesteatoma
 * keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis
 * DOID:0060360
 * hereditary renal cell carcinoma
 * class of disease
 * renal cell carcinoma inherited renal tumor
 * human disease
 * DOID:4455
 * hereditary retinal dystrophy
 * class of disease
 * fundus dystrophy genetic disease hereditary eye disease
 * Human disease
 * DOID:8500
 * hereditary sensory and autonomic neuropathy
 * class of disease
 * hereditary disorder peripheral neuropathy
 * congenital disorder of nervous system
 * DOID:0050548
 * C10.500.250 C10.574.500.493 C10.668.829.800.175 C16.131.666.310 C16.320.400.415
 * hereditary sensory and autonomic neuropathy type 1
 * class of disease
 * hereditary sensory and autonomic neuropathy
 * hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance
 * DOID:0070162
 * hereditary sensory and autonomic neuropathy type 1A
 * class of disease
 * hereditary sensory and autonomic neuropathy type 1 genetic disease autosomal dominant disease
 * hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has material basis in heterozygous mutation in the SPTLC1 gene on chromosome 9q22
 * DOID:0070152
 * hereditary sensory and autonomic neuropathy type 2
 * class of disease
 * hereditary sensory and autonomic neuropathy
 * hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood
 * DOID:0070161
 * hereditary sensory neuropathy X-linked
 * class of disease
 * hereditary sensory and autonomic neuropathy X-linked recessive disease
 * hereditary sensory neuropathy characterized by X-linked inheritance of slowly progressing neuropathy with onset in the first or second decade of life
 * DOID:0070159
 * hereditary sensory neuropathy type 1B
 * class of disease
 * hereditary sensory and autonomic neuropathy genetic disease autosomal dominant disease
 * hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has material basis in variation in the chromosome region 3p24-p22
 * DOID:0070148
 * hereditary spastic paraplegia 14
 * class of disease
 * hereditary spastic paraplegia pure or complex autosomal recessive spastic paraplegia autosomal recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 3q27-q28
 * DOID:0110767
 * hereditary spastic paraplegia 16
 * class of disease
 * hereditary spastic paraplegia pure or complex X-linked spastic paraplegia X-linked recessive disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2.
 * DOID:0110769
 * hereditary spastic paraplegia 19
 * class of disease
 * hereditary spastic paraplegia autosomal dominant pure spastic paraplegia autosomal dominant disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 9q
 * DOID:0110772
 * hereditary spastic paraplegia 24
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 13q14
 * DOID:0110775
 * hereditary spastic paraplegia 25
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 6q23-q24.1.
 * DOID:0110776
 * hereditary spastic paraplegia 27
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 10q22.1-q24.1.
 * DOID:0110778
 * hereditary spastic paraplegia 29
 * class of disease
 * hereditary spastic paraplegia autosomal dominant complex spastic paraplegia autosomal dominant disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1.
 * DOID:0110780
 * hereditary spastic paraplegia 32
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 14q12-q21
 * DOID:0110783
 * hereditary spastic paraplegia 34
 * class of disease
 * hereditary spastic paraplegia X-linked pure spastic paraplegia X-linked recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq24-q25
 * DOID:0110785
 * hereditary spastic paraplegia 36
 * class of disease
 * hereditary spastic paraplegia autosomal dominant complex spastic paraplegia autosomal dominant disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 12q23-q24
 * DOID:0110787
 * hereditary spastic paraplegia 37
 * class of disease
 * hereditary spastic paraplegia autosomal dominant pure spastic paraplegia autosomal dominant disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 8p21.1-q13.3.
 * DOID:0110788
 * hereditary spastic paraplegia 38
 * class of disease
 * hereditary spastic paraplegia autosomal dominant complex spastic paraplegia autosomal dominant disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15
 * DOID:0110789
 * hereditary spastic paraplegia 41
 * class of disease
 * hereditary spastic paraplegia autosomal dominant pure spastic paraplegia autosomal dominant disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2.
 * DOID:0110793
 * hereditary spherocytosis
 * class of disease
 * congenital hemolytic anemia spherocytosis disease
 * congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape
 * DOID:12971
 * C15.378.071.141.150.785 C16.320.070.785
 * Hereditary spherocytosis
 * hereditary spherocytosis type 3
 * class of disease
 * hereditary spherocytosis genetic disease autosomal recessive disease
 * A hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.
 * DOID:0110918
 * hernia of ovary and fallopian tube
 * class of disease
 * female reproductive system disease
 * Human disease
 * DOID:12735
 * heroin dependence
 * class of disease
 * opiate dependence
 * opiate dependence that involves the continued use of heroin despite problems related to use of the substance
 * DOID:9976
 * C25.775.675.400
 * herpes gestationis
 * class of disease
 * vesiculobullous skin disease dermatosis of pregnancy pemphigoid autoimmune skin disease disease
 * dermatosis of pregnancy
 * DOID:14482 DOID:0040098
 * C13.703.570 C17.800.865.700
 * Gestational pemphigoid
 * Pemphigoid gestationis - high mag.jpg
 * hexahydrophthalic anhydride allergic asthma
 * class of disease
 * allergic asthma
 * allergic asthma that has allergic trigger hexahydrophthalic anhydride
 * DOID:0040051
 * hexamethylene diisocyanate allergic asthma
 * class of disease
 * isocyanates allergic asthma
 * allergic asthma to isocyanates that has allergic trigger hexamethylene diisocyanate
 * DOID:0040040
 * hidradenitis
 * class of disease
 * sweat gland disease
 * human disease
 * DOID:2282
 * C17.800.946.315
 * hidradenoma
 * class of disease
 * sweat gland neoplasm epithelial skin neoplasm benign neoplasms by histologic type
 * human disease
 * DOID:3896
 * C04.557.470.035.175 C04.557.470.550.175
 * Hidradenoma
 * hidrocystoma
 * class of disease
 * apocrine sweat gland neoplasm benign neoplasm of sweat gland
 * Human disease
 * DOID:3893
 * C04.557.470.035.175.375 C04.557.470.550.175.375
 * Hidrocystoma
 * high pressure neurological syndrome
 * class of disease
 * central nervous system disease diving disorder
 * neurological and physiological disorder experienced by divers
 * DOID:3230
 * C10.228.566 C24.410
 * hilar lung carcinoma
 * class of disease
 * lung carcinoma lung hilum cancer
 * Human disease
 * DOID:8207
 * hilar lung neoplasm
 * class of disease
 * lung benign neoplasm
 * Human disease
 * DOID:5767
 * histidine metabolism disease
 * class of disease
 * amino acid metabolic disorder
 * amino acid metabolic disorder that involves deficiency in histidine
 * DOID:9265
 * histidinemia
 * class of disease
 * histidine metabolism disease
 * histidine metabolism disease that involves a deficiency of the enzyme histidase
 * DOID:0060168
 * L-histidine-skeletal.png
 * histiocytic and dendritic cell cancer
 * class of disease
 * hematologic cancer lymphoid hemopathy
 * sarcoma and hematologic cancer that derives from follicular lymphoma
 * DOID:5621
 * histiocytoid hemangioma
 * class of disease
 * hemangioma
 * Human disease
 * DOID:474
 * histiocytoma
 * class of disease
 * connective tissue neoplasm connective tissue benign neoplasm
 * Human disease
 * DOID:4231
 * C04.557.450.565.590.425
 * Histiocytoma
 * histiocytosis
 * class of disease
 * lymphatic system disease disease
 * lymphatic system disease that is characterized by an excessive number of histiocytes
 * DOID:3405
 * C15.604.250
 * Histiocytoses
 * histoplasmosis
 * class of disease
 * primary systemic mycosis genetic disease disease
 * human disease
 * DOID:1731
 * C01.150.703.450
 * Histoplasmosis
 * Histoplasmosis capsulatum.jpg
 * histoplasmosis meningitis
 * class of disease
 * fungal meningitis histoplasmosis
 * Human disease
 * DOID:12246
 * histoplasmosis retinitis
 * class of disease
 * retinitis
 * Human disease
 * DOID:11316
 * Presumed ocular histoplasmosis syndrome
 * histrionic personality disorder
 * class of disease
 * personality disorder disease
 * personality disorder characterized by excessive emotionality and attention-seeking
 * DOID:334
 * F03.675.400
 * Histrionic personality disorder
 * hole retinal cyst
 * class of disease
 * degeneration of macula and posterior pole retinoschisis and retinal cysts retinal perforation
 * Human disease
 * DOID:13214
 * holoprosencephaly
 * class of disease symptom or sign
 * nervous system malformations syndrome disease
 * congenital disorder of the nervous system
 * DOID:4621
 * C05.660.207.410 C10.500.034.875 C16.131.077.410 C16.131.260.380 C16.131.621.207.410 C16.131.666.034.875 C16.320.180.380
 * Holoprosencephaly
 * Alobar holoprosencephaly.jpg
 * holoprosencephaly 1
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * A holoprosencephaly that has material basis in variation in the chromosome region 21q22.3.
 * DOID:0110881
 * holoprosencephaly 2
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * holoprosencephaly that has material basis in mutation in the homeobox-containing SIX3 gene on chromosome 2p21
 * DOID:0110872
 * holoprosencephaly 5
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * holoprosencephaly that has material basis in heterozygous mutation in the ZIC2 gene on chromosome 13q32
 * DOID:0110878
 * holoprosencephaly 6
 * class of disease
 * holoprosencephaly genetic disease
 * A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.
 * DOID:0110874
 * holoprosencephaly 8
 * class of disease
 * holoprosencephaly genetic disease
 * holoprosencephaly that has material basis in variation in the chromosome region 14q13
 * DOID:0110879
 * holoprosencephaly 9
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * holoprosencephaly that has material basis in heterozygous mutation in the GLI2 gene on chromosome 2q14
 * DOID:0110873
 * homocarnosinosis
 * class of disease
 * gamma-amino butyric acid metabolism disorder inborn disorder of peptide metabolism encephalopathy
 * gamma-amino butyric acid metabolism disorder that is characterized by an excess of homocarnosine in the brain and has material basis in a deficiency of serum carnosinase in its ability to hydrolyze homocarnosine
 * DOID:0060177
 * hordeolum
 * class of disease symptom or sign
 * blepharitis eyelid disease disease
 * bacterial infection of an oil gland in the eyelid
 * DOID:9909
 * C01.150.252.289.400 C01.375.354.400 C11.294.354.400 C11.338.648
 * Stye
 * Stye02.jpg
 * hordeolum externum
 * class of disease
 * blepharitis
 * human disease
 * DOID:13134
 * horned turban snail allergy
 * class of disease
 * snail allergy
 * snail allergy triggered by Turbo cornutus
 * DOID:0060531
 * human cytomegalovirus infection
 * class of disease
 * viral infectious disease cytomegaloviral disease
 * human disease
 * DOID:0080827
 * human immunodeficiency virus infectious disease
 * class of disease
 * viral infectious disease Lentivirus infectious disease
 * disease affecting the human immune system
 * DOID:526
 * C20.673.480 C01.778.640.400 C01.925.782.815.616.400 C01.925.813.400 C01.221.250.875 C01.221.812.640.400 C12.100.937.640.400
 * human monocytic ehrlichiosis
 * class of disease
 * ehrlichiosis disease
 * human disease
 * DOID:0050026
 * Echaff.jpg
 * humeroradial synostosis
 * class of disease
 * synostosis
 * Human disease
 * DOID:0060467
 * hyaline body myopathy
 * class of disease
 * congenital myopathy
 * human disease
 * DOID:0111267
 * hyaline fibromatosis syndrome
 * class of disease
 * autosomal recessive disease connective tissue disease fibromatosis
 * human disease
 * DOID:0111669
 * hyalinizing trabecular adenoma
 * class of disease
 * follicular adenoma thyroid adenoma
 * human disease
 * DOID:6203
 * hydranencephaly with renal aplasia-dysplasia
 * class of disease
 * genetic disease autosomal recessive disease syndrome
 * human disease
 * DOID:0080327
 * hydrocele
 * class of disease
 * male reproductive system disease
 * human disease
 * DOID:9912
 * C12.294.882
 * Hydrocele
 * Gray1148.png
 * hydrolethalus syndrome 1
 * class of disease
 * hydrolethalus syndrome
 * human disease
 * DOID:0111355
 * hydrolethalus syndrome 2
 * class of disease
 * hydrolethalus syndrome
 * human disease
 * DOID:0111356
 * hydronephrosis
 * class of disease
 * urinary tract obstruction kidney disease disease
 * human disease
 * DOID:11111
 * C12.777.419.307 C13.351.968.419.307
 * Hydronephrosis
 * hydrophthalmos
 * class of disease
 * primary congenital glaucoma
 * Human disease
 * DOID:11212
 * C11.250.480 C11.525.381.407.480 C16.131.384.480 C16.614.438
 * hydrops of gallbladder
 * class of disease
 * gallbladder disease
 * Human disease
 * DOID:9717
 * hyper IgE recurrent infection syndrome 2
 * class of disease
 * autosomal recessive disease Job's syndrome
 * human disease
 * DOID:0080594
 * hyper IgE recurrent infection syndrome 3
 * class of disease
 * Job's syndrome autosomal recessive disease
 * human disease
 * DOID:0080595
 * hyper IgE recurrent infection syndrome 4
 * class of disease
 * autosomal recessive disease Job's syndrome
 * human disease
 * DOID:0080596
 * hyper-IgM syndrome type 4
 * class of disease
 * hyper IgM syndrome hyperimmunoglobulin syndrome
 * hyperimmunoglobulin syndrome characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process
 * DOID:0060760
 * hyperalphalipoproteinemia 1
 * class of disease
 * cholesterol-ester transfer protein deficiency autosomal dominant disease hyperalphalipoproteinemia
 * human disease
 * DOID:0111369
 * hyperandrogenism
 * class of disease
 * gonadal disease sex differentiation disease disease
 * medical condition characterized by excessive levels of androgens in the body
 * DOID:11613
 * C12.050.351.875.253.064.500 C12.050.351.875.253.090.750 C16.131.939.316.064.500 C16.131.939.316.129.750 C19.391.119.064.500 C19.391.119.090.750 C12.200.706.316.064.500 C12.200.706.316.090.750 C12.800.316.064.500 C12.800.316.090.750
 * Hyperandrogenism
 * hypercalcemia
 * class of disease
 * calcium metabolism disease disease
 * high calcium (Ca2+) level in the blood serum
 * DOID:12678
 * C18.452.174.451 C18.452.950.340
 * Hypercalcemia
 * hypercalcemic sarcoidosis
 * class of disease
 * sarcoidosis hypercalcemia
 * Human disease
 * DOID:13407
 * hypercalcemic type ovarian small cell carcinoma
 * class of disease
 * ovarian small cell carcinoma
 * Human disease
 * DOID:7651
 * hypercementosis
 * class of disease
 * teeth hard tissue disease
 * Human disease
 * DOID:12733
 * C07.793.422
 * hyperekplexia 1
 * class of disease
 * hyperekplexia genetic disease autosomal recessive disease autosomal dominant disease
 * hyperekplexia that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the GLRA1 gene on chromosome 5q32
 * DOID:0060696
 * C10.228.590
 * hyperekplexia 4
 * class of disease
 * hyperekplexia autosomal recessive disease
 * hyperekplexia that is characterized by extreme hypertonia, stiff and rigid appeareance and that has material basis in homozygous mutation in the ATAD1 gene on chromosome 10q23
 * DOID:0080581
 * hyperglobulinemic purpura
 * class of disease
 * purpura
 * Human disease
 * DOID:3325
 * C14.907.454.550 C15.378.100.802.250 C15.378.463.515.550 C23.550.414.950.250 C23.888.885.687.250
 * hyperglycemia
 * class of disease abnormally high value
 * glucose metabolism disease disease
 * human disease
 * DOID:4195
 * C18.452.394.952
 * Hyperglycemia
 * Hyperglycemia.png
 * hyperhomocysteinemia
 * class of disease
 * sulfuraminoacidemia amino acid metabolic disorder disease
 * amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood
 * DOID:9279
 * C16.320.565.100.480 C18.452.603.378 C18.452.648.100.480 C18.654.521.500.133.699.418
 * L-Homocysteine.svg
 * hyperimmunoglobulin syndrome
 * class of disease
 * B cell deficiency
 * Human disease
 * DOID:2959
 * hyperinsulinemia
 * class of disease
 * endocrine pancreas disease glucose metabolism disease pancreas disease
 * condition in which there are excess levels of insulin circulating in the blood relative to the level of glucose
 * DOID:2018
 * hyperlipoproteinemia type IV
 * class of disease
 * hyperlipidemia familial hyperlipidemia
 * human disease
 * DOID:1172
 * C16.320.565.398.487 C18.452.584.500.500.644.490 C18.452.584.500.500.851.500 C18.452.648.398.487 C18.452.584.563.487
 * hypermanganesemia with dystonia
 * class of disease
 * metal metabolism disorder
 * metal metabolism disorder that is characterized by involuntary, sustained muscle contractions (dystonia) and other uncontrolled movements resulting from excessive accumulation of manganese
 * DOID:0080535
 * hypermanganesemia with dystonia 1
 * class of disease
 * hypermanganesemia with dystonia
 * human disease
 * DOID:0080536
 * hypermethioninemia
 * class of disease
 * amino acid metabolic disorder
 * An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body.
 * DOID:0050544
 * hypermobility of coccyx
 * class of disease
 * spondyloarthropathy
 * Human disease
 * DOID:12537
 * hypermobility syndrome
 * class of disease
 * arthropathy joint hypermobility disease
 * human disease: joints that stretch farther than normal
 * DOID:13781
 * Hypermobility
 * Doublejointedfinger.JPG
 * hyperopia
 * class of disease symptom or sign
 * refractive error disease
 * visual defect which causes to see the far objects clearly and near objects unclearly
 * DOID:9834
 * C11.744.479
 * Hyperopia
 * Hypermetropia.svg
 * hyperostosis
 * class of disease
 * bone remodeling disease disease
 * human disease
 * DOID:205
 * C05.116.540
 * Hyperostosis
 * hyperphosphatemia
 * class of disease
 * phosphorus metabolism disease genetic disease disease
 * electrolyte disorder in which there is an elevated level of phosphate in the blood.
 * DOID:0050459
 * C18.452.750.199
 * Hyperphosphatemia
 * hyperphosphatemic familial tumoral calcinosis
 * class of disease
 * calcinosis genetic disease Tumoral calcinosis autosomal recessive disease
 * human disease
 * DOID:0111063
 * hyperpigmentation of eyelid
 * class of disease
 * pigmentation disorder eyelid disease
 * Human disease
 * DOID:10122
 * hyperpituitarism
 * class of disease
 * pituitary gland disease anterior pituitary gland disease disease
 * endocrine disease
 * DOID:2444
 * C10.228.140.617.738.250 C19.700.355
 * hyperprolinemia type 1
 * class of disease
 * hyperprolinemia autosomal recessive disease
 * hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the proline dehydrogenase gene on chromosome 22q11
 * DOID:0080542
 * hyperprolinemia type 2
 * class of disease
 * hyperprolinemia autosomal recessive disease
 * hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36
 * DOID:0080543
 * hyperprothrombinemia
 * class of disease
 * thrombophilia autosomal dominant disease
 * human disease
 * DOID:0080701
 * hypersecretion glaucoma
 * class of disease
 * glaucoma
 * Human disease
 * DOID:11148
 * hypersensitivity vasculitis
 * class of disease
 * type III hypersensitivity
 * Human disease
 * DOID:9809
 * C14.907.940.910 C20.543.520.910
 * hypersomnia
 * class of disease symptom or sign
 * sleep disorder neurological disorder sleep disturbance disease
 * excessive sleep
 * DOID:8619
 * C10.886.425.800.200 F03.870.400.800.200
 * hypersplenism
 * class of disease
 * splenic disease disease
 * Human disease
 * DOID:6376
 * C15.604.744.293
 * hypertensive encephalopathy
 * class of disease
 * intracranial hypertension encephalomyelitis disease
 * general brain dysfunction due to significantly high blood pressure
 * DOID:9427
 * C10.228.140.631.500
 * hypertensive retinopathy
 * class of disease
 * retinal disease complications of hypertension disease
 * Human disease
 * DOID:11561
 * C11.768.346 C14.907.489.815
 * Hypertensive retinopathy
 * Hypertensiveretinopathy.jpg
 * hyperthecosis
 * class of disease
 * ovarian disease
 * hyperplasia of the theca interna of the ovary
 * DOID:7347
 * hypertrichosis
 * class of disease
 * hair diseases epidermal disease genetic hair anomaly disease
 * hair disease characterized by hair growth that is abnormal in quantity or location
 * DOID:420
 * C17.800.329.875
 * Hypertrichosis
 * Alice Teennager.JPG
 * hypertrichosis of eyelid
 * class of disease
 * eyelid degenerative disease hypertrichosis nervous system heredodegenerative disease eyelid disease
 * hypertrichosis (disease) that involves the eyelid
 * DOID:11669
 * hypertrophic cardiomyopathy 1
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYH7 gene on chromosome 14q12
 * DOID:0110307
 * hypertrophic cardiomyopathy 10
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene
 * DOID:0110316
 * hypertrophic cardiomyopathy 11
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the ACTC1 gene on chromosome 15q14
 * DOID:0110317
 * hypertrophic cardiomyopathy 12
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the CSRP3 gene on chromosome 11p15
 * DOID:0110318
 * hypertrophic cardiomyopathy 13
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21
 * DOID:0110319
 * hypertrophic cardiomyopathy 14
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in mutation in the MYH6 gene
 * DOID:0110320
 * hypertrophic cardiomyopathy 15
 * class of disease
 * familial hypertrophic cardiomyopathy
 * human disease
 * DOID:0110321
 * hypertrophic cardiomyopathy 16
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26
 * DOID:0110322
 * hypertrophic cardiomyopathy 17
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12
 * DOID:0110323
 * hypertrophic cardiomyopathy 18
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
 * DOID:0110324
 * hypertrophic cardiomyopathy 2
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)
 * DOID:0110308
 * hypertrophic cardiomyopathy 20
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
 * DOID:0110326
 * hypertrophic cardiomyopathy 21
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.
 * DOID:0110311
 * hypertrophic cardiomyopathy 25
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TCAP gene on chromosome 17q12
 * DOID:0110328
 * hypertrophic cardiomyopathy 3
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22
 * DOID:0110309
 * hypertrophic cardiomyopathy 4
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11
 * DOID:0110310
 * hypertrophic cardiomyopathy 6
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2)
 * DOID:0110312
 * hypertrophic cardiomyopathy 7
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
 * DOID:0110313
 * hypertrophic cardiomyopathy 8
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene
 * DOID:0110314
 * hypertrophic elongation of cervix
 * class of disease
 * cervix disease
 * Human disease
 * DOID:2251
 * hypertrophic pyloric stenosis
 * class of disease
 * pyloric stenosis
 * pyloric stenosis characterized by the enlargement of the muscle surrounding the pylorus, causing severe projectile non-bilious vomiting
 * DOID:12638
 * C06.405.748.340.690.500
 * hypertrophy of tongue papillae
 * class of disease
 * tongue disease
 * Human disease
 * DOID:13333
 * hypertropia
 * class of disease
 * strabismus disease
 * Human disease
 * DOID:9837
 * Hypertropia
 * hyperuricemia
 * class of disease
 * acquired metabolic disease disease
 * acquired metabolic disease that has material basis in an abnormally high level of uric acid in the blood.
 * DOID:1920
 * C23.550.449
 * Hyperuricemia
 * hypervitaminosis A
 * class of disease
 * overnutrition hypervitaminosis disease
 * Human disease
 * DOID:9972
 * C18.654.301
 * All-trans-Retinol2.svg
 * hypervitaminosis D
 * class of disease
 * overnutrition hypervitaminosis disease
 * excess of Vitamin D leading to abnormalities
 * DOID:9971
 * hypoactive sexual desire disorder
 * class of disease
 * psychosexual disorder sexual dysfunction disease
 * sexual dysfunction
 * DOID:13868
 * F03.835
 * hypobetalipoproteinemia
 * class of disease
 * hypolipoproteinemia disease
 * hypolipoproteinemia characterized by permanently low levels of apolipoprotein B and LDL cholesterol resulting from an impaired ability to absorb and transport fats
 * DOID:1390
 * C16.320.565.398.500.440 C18.452.584.500.875.440 C18.452.648.398.500.440 C18.452.584.563.500.440
 * hypochondriasis
 * class of disease
 * somatoform disorder nosophobia disease
 * somatoform disorder that involves an excessive preoccupation or worry about having a serious illness
 * DOID:12883
 * F03.875.450
 * hypochondrogenesis
 * class of disease
 * osteochondrodysplasia achondrogenesis genetic disease spinal disease monogenic disease
 * human disease
 * DOID:0080044
 * hypochromic anemia
 * class of disease
 * anemia
 * generic term for any type of anemia in which the red blood cells (erythrocytes) are paler than normal
 * DOID:11759
 * C15.378.071.196
 * hypoglossal nerve disease
 * class of disease
 * glossopharyngeal nerve disease
 * human disease
 * DOID:13814
 * C10.292.525
 * hypoglossal nerve neoplasm
 * class of disease
 * cranial nerve neoplasm hypoglossal nerve disease
 * Human disease
 * DOID:3198
 * hypoglycemic coma
 * class of disease
 * encephalopathy coma hypoglycemia
 * human disease
 * DOID:1607
 * hypogonadism
 * class of disease
 * gonadal disease disease
 * endocrine disease
 * DOID:1924
 * C19.391.482
 * Hypogonadism
 * hypogonadotropic hypogonadism 12 with or without anosmia
 * class of disease
 * hypogonadotropic hypogonadism genetic disease
 * hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21
 * DOID:0090072
 * hypogonadotropic hypogonadism 16 with or without anosmia
 * class of disease
 * hypogonadotropic hypogonadism genetic disease autosomal dominant disease
 * hypogonadotropic hypogonadism that has material basis in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes
 * DOID:0090080
 * hypogonadotropic hypogonadism 2 with or without anosmia
 * class of disease
 * hypogonadotropic hypogonadism genetic disease
 * hypogonadotropic hypogonadism that has material basis in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes
 * DOID:0090083
 * hypohidrosis
 * class of disease
 * sweat gland disease abnormal sudomotor regulation
 * Human disease
 * DOID:11155
 * C17.800.946.370
 * hypolipoproteinemia
 * class of disease
 * lipid metabolism disorder disease
 * Human disease
 * DOID:1387
 * C16.320.565.398.500 C18.452.584.500.875 C18.452.648.398.500 C18.452.584.563.500
 * hypomyelinating leukodystrophy
 * class of disease
 * leukodystrophy Hereditary CNS demyelinating disease
 * leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system
 * DOID:0060786
 * hypomyelinating leukodystrophy 14
 * class of disease
 * hypomyelinating leukodystrophy autosomal recessive disease
 * human disease
 * DOID:0080296
 * hypomyelinating leukoencephalopathy
 * class of disease
 * spinocerebellar ataxia
 * Human disease
 * DOID:0050987
 * hypoparathyroidism, familial isolated
 * class of disease
 * genetic hypoparathyroidism hypoparathyroidism
 * human disease
 * DOID:0111387
 * hypopharynx cancer
 * class of disease
 * carcinoma pharyngeal cancer neoplasm of hypopharynx
 * pharynx cancer that is located in the hypopharynx
 * DOID:8533
 * Hypopharyngeal cancer
 * HypopharynxCa.jpg
 * hypophosphatemic nephrolithiasis/osteoporosis
 * class of disease
 * kidney disease familial hypophosphatemia
 * human disease
 * DOID:0080655
 * hypopigmentation of eyelid
 * class of disease
 * eyelid degenerative disease pigmentation disorder eyelid disease
 * human disease
 * DOID:11668
 * hypopyon
 * class of disease symptom or sign
 * iridocyclitis eye symptom disease
 * Human disease
 * DOID:10443
 * Hypopyon
 * Hypopyon.jpg
 * hypopyon ulcer
 * class of disease
 * hypopyon corneal ulcer
 * Human disease
 * DOID:10442
 * hypospadias
 * class of disease
 * non-syndromic urogenital tract malformation of male penile disease congenital disorder disease
 * condition in which the urethra does not open from the head of the penis
 * DOID:10892
 * C12.294.494.400 C12.706.516 C13.351.875.466 C16.131.939.516
 * Hypospadias
 * Hypospadias3.jpg
 * hypothalamic disease
 * class of disease
 * thalamic disease encephalopathy
 * human disease
 * DOID:1931
 * C10.228.140.617
 * hypothalamic neoplasm
 * class of disease
 * diencephalic neoplasm brain cancer connective tissue neoplasm hypothalamic disease
 * human disease
 * DOID:3644
 * C04.588.614.250.195.885.500 C10.228.140.211.885.500 C10.228.140.617.477 C10.551.240.250.700.500
 * hypothyroidism
 * class of disease
 * thyroid gland disease disease
 * human disease
 * DOID:1459
 * C19.874.482
 * Hypothyroidism
 * hypotonia-cystinuria syndrome
 * class of disease
 * syndrome cystinuria chromosomal deletion syndrome
 * human disease
 * DOID:0060858
 * hypotrichosis 1
 * class of disease
 * hypotrichosis genetic disease autosomal dominant disease
 * A hypotrichosis that has material basis in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.
 * DOID:0110698
 * hypotrichosis 10
 * class of disease
 * hypotrichosis genetic disease autosomal recessive disease
 * A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.
 * DOID:0110707
 * hypotrichosis 14
 * class of disease
 * hypotrichosis simplex hypotrichosis
 * human disease
 * DOID:0080582
 * hypotrichosis 4
 * class of disease
 * hypotrichosis genetic disease autosomal dominant disease
 * A hypotrichosis that has material basis in a autosomal dominant mutation of HR on chromosome 8p21.3.
 * DOID:0110701
 * hypotrichosis 5
 * class of disease
 * hypotrichosis genetic disease autosomal dominant disease
 * A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3.
 * DOID:0110702
 * hypotrichosis 9
 * class of disease
 * hypotrichosis genetic disease autosomal recessive disease
 * A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 10q11.23-q22.3.
 * DOID:0110706
 * hypotrichosis of eyelid
 * class of disease
 * eyelid degenerative disease hypotrichosis eyelid disease
 * hypotrichosis that involves the eyelid
 * DOID:11671
 * hypotropia
 * class of disease
 * strabismus
 * Human disease
 * DOID:9841
 * ichthyosis follicularis-alopecia-photophobia syndrome 1
 * class of disease
 * X-linked recessive disease syndrome Ichthyosis follicularis with alopecia and photophobia syndrome
 * human disease
 * DOID:0111821
 * ideomotor apraxia
 * class of disease
 * apraxia
 * Human disease
 * DOID:4627
 * C10.597.606.881.350.200 C23.888.592.604.882.350.200 F01.700.875.350.200
 * idiopathic corneal edema
 * class of disease
 * corneal edema
 * Human disease
 * DOID:11033
 * idiopathic generalized epilepsy 11
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111312
 * idiopathic generalized epilepsy 12
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111313
 * idiopathic generalized epilepsy 13
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111314
 * idiopathic generalized epilepsy 14
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111315
 * idiopathic generalized epilepsy 15
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111316
 * idiopathic generalized epilepsy 2
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111317
 * idiopathic generalized epilepsy 3
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111318
 * idiopathic generalized epilepsy 4
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111319
 * idiopathic generalized epilepsy 5
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111320
 * idiopathic generalized epilepsy 7
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111321
 * idiopathic generalized epilepsy 9
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111323
 * idiopathic orbital inflammatory disease
 * class of disease
 * orbital granuloma chronic orbital inflammation
 * Human disease
 * DOID:9369
 * C11.675.679
 * Inflammatory pseudotumor - Plasma cell granuloma Case 176 (5601449638).jpg
 * idiopathic peripheral autonomic neuropathy
 * class of disease
 * autonomic nervous system disease autonomic peripheral neuropathy
 * human disease
 * DOID:11488
 * idiopathic progressive polyneuropathy
 * class of disease
 * polyneuropathy
 * human disease
 * DOID:10593
 * idiopathic pulmonary fibrosis
 * class of disease
 * idiopathic interstitial pneumonia pulmonary fibrosis
 * chronic, irreversible and ultimately fatal disease characterized by a progressive decline in lung function
 * DOID:0050156
 * C08.381.483.487.500 C08.381.765.500
 * Idiopathic pulmonary fibrosis
 * idiopathic scoliosis
 * class of disease
 * scoliosis
 * scoliosis with no known cause
 * DOID:0060250
 * ileal neoplasm
 * class of disease
 * small intestine neoplasm ileal disease
 * human disease
 * DOID:10156
 * C04.588.274.476.411.501 C06.301.371.411.501 C06.405.249.411.501 C06.405.469.420.501 C06.405.469.491.501
 * ileitis
 * class of disease
 * Crohn's disease enteritis
 * inflammatory bowel disease characterized by inflammation located in ileum, has symptom diarrhea, has symptom abdominal pain, often in the right lower quadrant, has symptom weight loss
 * DOID:0060189
 * C06.405.205.462.624 C06.405.469.326.875 C06.405.469.420.520
 * Ileitis
 * ileum cancer
 * class of disease
 * small intestine cancer ileal neoplasm
 * small intestine cancer that is located in the ileum
 * DOID:10153
 * ileus
 * class of disease
 * bowel obstruction disease
 * human disease characterized by impairment of intestinal peristalsis; in modern language usually excludes mechanical bowel obstruction
 * DOID:8440
 * C06.405.469.531.492
 * Ileus
 * iliac vein thrombophlebitis
 * class of disease
 * thrombophlebitis
 * Human disease
 * DOID:10880
 * immature cataract
 * class of disease
 * senile cataract
 * Human disease
 * DOID:10997
 * immature teratoma
 * class of disease
 * teratoma
 * Human disease
 * DOID:5563
 * immature teratoma of ovary
 * class of disease
 * malignant ovarian germ cell neoplasm malignant non-dysgerminomatous germ cell tumor of ovary ovarian biphasic or triphasic teratoma
 * Human disease
 * DOID:6331
 * immune disorder
 * class of disease
 * disease of anatomical entity
 * a disease of the immune system
 * DOID:2914
 * C20
 * Diseases and disorders of the immune system
 * immune system cancer
 * class of disease
 * organ system cancer immune disorder
 * organ system cancer located in the immune system that is characterized by uncontrolled cellular proliferation in organs of the immune system
 * DOID:0060083
 * immune system organ benign neoplasm
 * class of disease
 * organ system benign neoplasm immune disorder
 * organ system benign neoplasm located in the immune system organs
 * DOID:0060092
 * immune-complex glomerulonephritis
 * class of disease
 * glomerulonephritis
 * Human disease
 * DOID:4784
 * immunodeficiency 11A
 * class of disease
 * autosomal recessive disease severe combined immunodeficiency
 * human disease
 * DOID:0111957
 * immunodeficiency 11B
 * class of disease
 * autosomal dominant disease T cell deficiency
 * human disease
 * DOID:0111958
 * immunodeficiency 15A
 * class of disease
 * autosomal dominant disease combined immunodeficiency severe combined immunodeficiency due to IKK2 deficiency
 * human disease
 * DOID:0111960
 * immunodeficiency 15B
 * class of disease
 * severe combined immunodeficiency autosomal recessive disease severe combined immunodeficiency due to IKK2 deficiency
 * human disease
 * DOID:0111959
 * immunodeficiency 18
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease
 * human disease
 * DOID:0111971
 * immunodeficiency 19
 * class of disease
 * autosomal recessive disease severe combined immunodeficiency
 * human disease
 * DOID:0111972
 * immunodeficiency 28
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease
 * human disease
 * DOID:0111995
 * immunodeficiency 32A
 * class of disease
 * autosomal dominant disease dendritic cell deficiency
 * human disease
 * DOID:0111986
 * immunodeficiency 32B
 * class of disease
 * monocyte, dendritic cell, and NK cell deficiency autosomal recessive disease
 * human disease
 * DOID:0111985
 * immunodeficiency 45
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
 * human disease
 * DOID:0111994
 * immunodeficiency 51
 * class of disease
 * primary immunodeficiency disease autosomal recessive disease
 * human disease
 * DOID:0111996
 * immunodeficiency 52
 * class of disease
 * T cell deficiency autosomal recessive disease
 * human disease
 * DOID:0111983
 * immunodeficiency 53
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0111992
 * immunodeficiency 55
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0111993
 * immunodeficiency 57
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease
 * human disease
 * DOID:0111952
 * immunodeficiency 58
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0111984
 * immunodeficiency 59
 * class of disease
 * autosomal recessive disease B cell and dendritic cell deficiency
 * human disease
 * DOID:0111974
 * immunodeficiency 60
 * class of disease
 * combined immunodeficiency autosomal dominant disease
 * human disease
 * DOID:0111954
 * immunodeficiency 62
 * class of disease
 * autosomal recessive disease B cell deficiency
 * human disease
 * DOID:0111991
 * immunodeficiency 63
 * class of disease
 * autosomal recessive disease T cell and NK cell immunodeficiency
 * human disease
 * DOID:0111997
 * immunodeficiency 64
 * class of disease
 * T cell, B cell, and NK cell deficiency autosomal recessive disease
 * human disease
 * DOID:0111980
 * immunodeficiency 65
 * class of disease
 * primary immunodeficiency disease autosomal recessive disease
 * human disease
 * DOID:0111978
 * immunodeficiency 66
 * class of disease
 * primary immunodeficiency disease autosomal recessive disease
 * human disease
 * DOID:0111998
 * immunodeficiency 69
 * class of disease
 * autosomal recessive disease T cell and NK cell immunodeficiency
 * human disease
 * DOID:0112006
 * immunodeficiency 70
 * class of disease
 * autosomal dominant disease combined immunodeficiency
 * human disease
 * DOID:0112005
 * immunodeficiency 71
 * class of disease
 * combined immunodeficiency autosomal recessive disease
 * human disease
 * DOID:0112004
 * immunodeficiency 72
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0112015
 * immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
 * class of disease
 * autosomal dominant disease combined immunodeficiency
 * human disease
 * DOID:0112061
 * immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
 * class of disease
 * combined immunodeficiency autosomal recessive disease
 * human disease
 * DOID:0112062
 * immunodeficiency-centromeric instability-facial anomalies syndrome
 * class of disease
 * autosomal recessive disease DNA repair defect other than combined T-cell and B-cell immunodeficiencies syndrome
 * autosomal recessive disease characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases
 * DOID:0090007
 * immunoglobulin A deficiency
 * class of disease
 * selective immunoglobulin deficiency disease B cell deficiency genetic disease disease
 * dysgammaglobulinemia characterized by a deficiency of immunoglobulin A
 * DOID:0060025
 * C15.378.147.333.500 C20.673.430.500
 * immunoglobulin beta deficiency
 * class of disease
 * B cell deficiency
 * Human disease
 * DOID:0060026
 * imperforate anus
 * class of disease
 * congenital disorder atresia anorectal anomalies anal disease
 * congenital disorder of digestive system
 * DOID:10488
 * C06.198.050 C16.131.314.094
 * Imperforate anus
 * Rectovestibular fistula in females.jpg
 * impulse control disorder
 * class of disease
 * mental disorder disease
 * disease of mental health that involves a failure to resist an impulsive act or behaviour that may be harmful to self or others
 * DOID:10937
 * F03.250
 * Habit and impulse disorders
 * in situ carcinoma
 * class of disease
 * pre-malignant neoplasm In situ neoplasm disease
 * human disease
 * DOID:8719
 * C04.557.470.200.240
 * Carcinomas in situ
 * In situ carcinoma-en.svg
 * inborn errors of purine–pyrimidine metabolism
 * class of disease
 * inherited metabolic disorder
 * inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism
 * DOID:653
 * C16.320.565.798 C18.452.648.798
 * inborn errors pyruvate metabolism
 * class of disease
 * carbohydrate metabolic disorder
 * human disease
 * DOID:3648
 * C16.320.565.202.810 C18.452.648.202.810
 * inborn metabolic brain disease
 * class of disease
 * metabolic brain disease
 * Human disease
 * DOID:889
 * C10.228.140.163.100 C16.320.565.189 C18.452.132.100 C18.452.648.189
 * inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
 * class of disease
 * inclusion body myopathy with Paget disease of bone and frontotemporal dementia autosomal dominant disease
 * human disease
 * DOID:0111385
 * inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
 * class of disease
 * inclusion body myopathy with Paget disease of bone and frontotemporal dementia autosomal dominant disease
 * human disease
 * DOID:0111384
 * inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
 * class of disease
 * inclusion body myopathy with Paget disease of bone and frontotemporal dementia autosomal dominant disease
 * human disease
 * DOID:0111386
 * incontinentia pigmenti achromians
 * class of disease
 * skin disease disease
 * Human disease
 * DOID:3156
 * indeterminate leprosy
 * class of disease
 * leprosy paucibacillary leprosy
 * leprosy that is an early form of the disease which causes one to a few hypopigmented or erythematous macules
 * DOID:11851
 * indolent myeloma
 * class of disease
 * smouldering myeloma multiple myeloma
 * Human disease
 * DOID:9550
 * indolent systemic mastocytosis
 * class of disease
 * mastocytoma systemic mastocytosis
 * human disease
 * DOID:4660
 * infancy electroclinical syndrome
 * class of disease
 * electroclinical syndrome epilepsy syndrome Epilepsy in children
 * electroclinical syndrome with onset in infancy occurring between birth and one year of age
 * DOID:0050703
 * infant gynecomastia
 * class of disease
 * breast disease gynecomastia
 * human disease
 * DOID:11603
 * infantile epileptic encephalopathy
 * class of disease
 * infancy electroclinical syndrome childhood onset epileptic encephalopathy West syndrome
 * Human disease
 * DOID:2481
 * C10.228.140.490.375.760 C10.228.140.490.493.875
 * infantile hypophosphatasia
 * class of disease
 * hypophosphatasia
 * A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.
 * DOID:0110914
 * infantile or early childhood epileptic encephalopathy 1
 * class of disease
 * electroclinical syndrome infantile epileptic encephalopathy
 * human disease
 * DOID:0080472
 * infantile or early childhood epileptic encephalopathy 2
 * class of disease
 * electroclinical syndrome autosomal dominant disease
 * electroclinical syndrome characterized by onset of seizures in infancy or early childhood, global developmental delay and variable intellectual disability that has material basis in heterozygous mutation in the GABRB2 gene on chromosome 5q34
 * DOID:0080471
 * infantile osteopetrosis with neuroaxonal dysplasia
 * class of disease
 * neuroaxonal dystrophy osteopetrosis
 * This syndrome is characterized by osteopetrosis, agenesis of the corpus callosum, cerebral atrophy and a small hippocampus
 * DOID:0070343
 * infantile-onset distal myopathy
 * class of disease
 * distal muscular dystrophy
 * distal muscular dystrophy characterized by autosomal dominant inheritance, infantile onset and progressive disease development
 * DOID:0070196
 * infected hydrocele
 * class of disease
 * hydrocele
 * Human disease
 * DOID:9911
 * infectious disease
 * class of disease
 * disease infection associated with diseases
 * disease caused by infection of pathogenic biological agents in a host organism
 * DOID:0050117
 * C01.539.221
 * Infectious diseases and disorders
 * Malaria.jpg
 * infective endocarditis
 * class of disease
 * endocarditis cardiovascular Infection infectious disease disease
 * endocarditis that is characterized by inflammation of the endocardium caused by infectious agents.
 * DOID:0060000
 * Haemophilus parainfluenzae Endocarditis PHIL 851 lores.jpg
 * infective urethral stricture
 * class of disease
 * urethral stricture
 * Human disease
 * DOID:13658
 * inferior myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5850
 * C14.280.647.500.187 C14.907.585.500.187 C23.550.513.355.750.187 C23.550.717.489.750.187
 * inferolateral myocardial infarct
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5852
 * infertility
 * class of disease symptom or sign
 * reproductive system disease reproductive system symptom disease
 * inability of a person, animal or plant to reproduce by natural means that is no intervention of contraceptive techniques
 * DOID:5223
 * C12.294.365 C13.351.500.365
 * Infertility
 * Infertility causes.png
 * infertility due to extratesticular cause
 * class of disease
 * male infertility
 * Human disease
 * DOID:14096
 * infiltrating angiolipoma
 * class of disease
 * angiolipoma
 * Human disease
 * DOID:3615
 * infiltrating bladder lymphoepithelioma-like carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * human disease
 * DOID:7600
 * infiltrating bladder urothelial carcinoma sarcomatoid variant
 * class of disease
 * invasive bladder transitional cell carcinoma sarcomatoid transitional cell carcinoma
 * Human disease
 * DOID:7553
 * infiltrating lipoma
 * class of disease
 * lipoma
 * Human disease
 * DOID:7014
 * infiltrating nipple syringomatous adenoma
 * class of disease
 * nipple neoplasm
 * Human disease
 * DOID:7839
 * infiltrating renal pelvis transitional cell carcinoma
 * class of disease
 * renal pelvis transitional cell carcinoma
 * Human disease
 * DOID:0050620
 * infiltrating ureter transitional cell carcinoma
 * class of disease
 * ureter transitional cell carcinoma
 * Human disease
 * DOID:6845
 * infiltrative basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4299
 * inflamed seborrheic keratosis
 * class of disease
 * seborrheic keratosis
 * Human disease
 * DOID:11685
 * inflammatory MFH
 * class of disease
 * malignant fibrous histiocytoma
 * Human disease
 * DOID:6192
 * inflammatory and toxic neuropathy
 * class of disease
 * peripheral neuropathy acquired peripheral neuropathy
 * Human disease
 * DOID:2537
 * inflammatory bowel disease 1
 * class of disease
 * inflammatory bowel diseases genetic disease
 * An inflammatory bowel disease that has material basis in mutations in the NOD2 gene on chromosome 16q12.1.
 * DOID:0110892
 * inflammatory bowel disease 11
 * class of disease
 * inflammatory bowel diseases genetic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 7q22
 * DOID:0110894
 * inflammatory bowel disease 12
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 3p21.3
 * DOID:0110887
 * inflammatory bowel disease 13
 * class of disease
 * inflammatory bowel diseases genetic disease
 * An inflammatory bowel disease that has material basis in variation in the ABCB1 gene on chromosome 7q21.1.
 * DOID:0110893
 * inflammatory bowel disease 15
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 10q21
 * DOID:0110897
 * inflammatory bowel disease 16
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 9q32
 * DOID:0110896
 * inflammatory bowel disease 17
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the IL23R gene on chromosome 1p31.3.
 * DOID:0110883
 * inflammatory bowel disease 18
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 5p13.1.
 * DOID:0110888
 * inflammatory bowel disease 2
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 12p13.2-q24.1.
 * DOID:0110900
 * inflammatory bowel disease 20
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 10q23-q24
 * DOID:0110898
 * inflammatory bowel disease 21
 * class of disease
 * inflammatory bowel diseases genetic disease autosomal dominant disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 18p11
 * DOID:0110906
 * inflammatory bowel disease 22
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 17q21.2.
 * DOID:0110905
 * inflammatory bowel disease 23
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 1q32.1.
 * DOID:0110884
 * inflammatory bowel disease 24
 * class of disease
 * inflammatory bowel diseases genetic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome 20q13
 * DOID:0110908
 * inflammatory bowel disease 26
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 12q15
 * DOID:0110901
 * inflammatory bowel disease 27
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 13q13.3
 * DOID:0110902
 * inflammatory bowel disease 3
 * class of disease
 * inflammatory bowel diseases genetic disease autosomal dominant disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 6p21.3.
 * DOID:0110891
 * inflammatory bowel disease 4
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 14q11-q12
 * DOID:0110903
 * inflammatory bowel disease 5
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 5q31
 * DOID:0110889
 * inflammatory bowel disease 6
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 19p13
 * DOID:0110907
 * inflammatory bowel disease 7
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 1p36
 * DOID:0110882
 * inflammatory bowel disease 8
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 16p
 * DOID:0110904
 * inflammatory bowel disease 9
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 3p26
 * DOID:0110886
 * inflammatory bowel diseases
 * class of disease
 * intestinal disease immune disorder disease
 * intestinal disease characterized by inflammation located in all parts of digestive tract
 * DOID:0050589
 * C06.405.205.731 C06.405.469.432
 * Inflammatory bowel diseases
 * Cryptitis high mag.jpg
 * inflammatory breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:6263
 * inflammatory diarrhea
 * class of disease
 * diarrhea mucositis
 * Human disease
 * DOID:0050132
 * inflammatory leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5251
 * inflammatory liposarcoma
 * class of disease
 * atypical lipomatous tumor
 * Human disease
 * DOID:8233
 * inflammatory myofibroblastic tumour
 * class of disease
 * mesenchymal cell neoplasm connective tissue benign neoplasm
 * mesenchymal cell neoplasm that has material basis in myofibroblastic cells admixed with inflammatory cells
 * DOID:0050905
 * Inflammatory myofibroblastic tumour
 * inflammatory spondylopathy
 * class of disease
 * spondylitis
 * Human disease
 * DOID:12105
 * infratentorial cancer
 * class of disease
 * brain cancer infratentorial neoplasm
 * brain cancer that is located in the infratentorial region
 * DOID:4706
 * infundibulocystic basal cell carcinoma
 * class of disease
 * basal-cell carcinoma inherited skin tumor
 * Human disease
 * DOID:4279
 * inguinal hernia
 * class of disease
 * intestinal disease disease
 * intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal
 * DOID:0060320
 * C23.300.707.374.875
 * Inguinal hernia
 * Inguinalhernia.gif
 * inherited metabolic disorder
 * class of disease
 * genetic disease rare disease metabolic disease disease
 * class of disease including endocrine diseases, nutritional diseases and metabolic diseases
 * DOID:655
 * C16.320.565 C18.452.648
 * Inborn errors of metabolism
 * inhibited female orgasm
 * class of disease
 * female reproductive system disease anorgasmia female orgasm
 * Human disease
 * DOID:7518 DOID:11110
 * inner ear cancer
 * class of disease
 * auricular cancer inner ear neoplasm
 * Human disease
 * DOID:5102
 * inner ear disease
 * class of disease
 * ear disease
 * human disease
 * DOID:2952 DOID:4539
 * C09.218.568
 * insulinoma
 * class of disease
 * pancreatic cystadenoma benign neoplasms by histologic type islet cell adenoma disease
 * tumor that produces too much insulin
 * DOID:3892
 * C04.557.470.035.100.852 C04.588.274.761.249.500 C04.588.322.475.249.500 C06.301.761.249.500 C06.689.667.249.500 C19.344.421.249.500
 * Insulinoma
 * Pancreatic insulinoma (2).JPG
 * integrative agnosia
 * class of disease
 * agnosia apperceptive agnosia
 * agnosia that is a loss of the ability to integrate these elements together into comprehensible perceptual wholes while recognizing elements of the whole
 * DOID:0060143
 * integumentary system benign neoplasm
 * class of disease
 * organ system benign neoplasm integumentary system neoplasm
 * organ system benign neoplasm located in the integumentary system organs
 * DOID:0060121
 * integumentary system cancer
 * class of disease
 * organ system cancer integumentary system neoplasm integumentary system disease
 * organ system cancer that is located in the skin, hair and nails
 * DOID:0060122
 * integumentary system disease
 * class of disease
 * disease of anatomical entity
 * disease of anatomical entity that is located in the integumentary system comprising the skin and its appendages
 * DOID:16
 * intellectual developmental disorder with short stature and behavioral abnormalities
 * class of disease
 * syndrome autosomal recessive disease syndromic intellectual disability
 * human disease
 * DOID:0111674
 * intellectual disability
 * class of disease
 * specific developmental disorder cognitive deficit disability disease
 * generalized neurodevelopmental disorder
 * DOID:1059
 * C23.888.592.604.646 C10.597.606.360 F01.700.687 F03.625.539
 * Intellectual disabilities
 * interdigitating dendritic cell sarcoma
 * class of disease
 * histiocytic and dendritic cell cancer dendritic cell sarcoma
 * histiocytic and dendritic cell cancer that effect dendritic cells
 * DOID:7848
 * C04.557.227.199 C15.604.250.390.199
 * interleukin-7 receptor alpha deficiency
 * class of disease
 * severe combined immunodeficiency
 * human disease
 * DOID:0060015
 * intermediate malignant teratoma
 * class of disease
 * immature teratoma
 * Human disease
 * DOID:7202
 * intermediate uveitis
 * class of disease
 * uveitis
 * human disease
 * DOID:12732
 * C11.941.879.900
 * Intermediate uveitis
 * intermittent asthma
 * class of disease
 * chronic asthma
 * human disease
 * DOID:0080812
 * intermittent explosive disorder
 * class of disease
 * impulse control disorder disease
 * Mood disorder identified by frequent episodes of anger and rage
 * DOID:12401
 * intermittent proptosis
 * class of disease
 * orbital disease exophthalmos
 * Human disease
 * DOID:12363
 * intermittent squint
 * class of disease
 * strabismus
 * Human disease
 * DOID:1942
 * intermixed schwannian stroma-rich ganglioneuroblastoma
 * class of disease
 * ganglioneuroblastoma
 * Human disease
 * DOID:5194
 * internal hemorrhoid
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9749
 * internal resorption
 * class of disease
 * tooth resorption
 * human disease
 * DOID:13239
 * internuclear ophthalmoplegia
 * class of disease
 * ophthalmoplegia strabismus
 * Human disease
 * DOID:538
 * Internuclear ophthalmoplegia.jpg
 * interstitial keratitis
 * class of disease
 * connective tissue disease deep keratitis
 * human disease
 * DOID:9857
 * interstitial myocarditis
 * class of disease
 * mediastinitis myocarditis
 * Inflammation of the heart characterized by infiltration of the interstitial tissues by inflammatory cells, histiocytes, and the formation of granulomas. Giant cells are often present.
 * DOID:817
 * interstitial nephritis
 * class of disease
 * nephritis kidney disease disease
 * type of nephritis affecting the interstitium of the kidneys surrounding the tubules
 * DOID:1063
 * C12.200.777.419.570.643 C12.050.351.968.419.570.643 C12.950.419.570.643
 * Tubulointerstitial disease
 * interval angle-closure glaucoma
 * class of disease
 * primary angle-closure glaucoma
 * Human disease
 * DOID:13549
 * intestinal atresia
 * class of disease
 * intestinal disease intestinal malformation
 * congenital disorder of digestive system
 * DOID:10486
 * C06.198.719 C06.405.469.445 C16.131.314.466
 * Intestinal atresia
 * DuodAtres.png
 * intestinal benign neoplasm
 * class of disease
 * gastrointestinal system benign neoplasm intestinal neoplasm intestinal disease
 * gastrointestinal system benign neoplasm that is located in the intestine
 * DOID:4610
 * intestinal cancer
 * class of disease
 * gastrointestinal system cancer intestinal neoplasm intestinal disease
 * gastrointestinal system cancer that is located in the intestine
 * DOID:10155
 * Intestinal cancers
 * intestinal disaccharidase deficiency
 * class of disease
 * metabolic disease with intestinal involvement intestinal disease carbohydrate metabolic disorder
 * Human disease
 * DOID:9868
 * intestinal disease
 * class of disease
 * gastrointestinal system disease
 * gastrointestinal system disease that is located in the intestine
 * DOID:5295
 * C06.405.469
 * Diseases and disorders of intestines
 * intestinal impaction
 * class of disease
 * bowel obstruction
 * Human disease
 * DOID:8448
 * intestinal neuroendocrine benign tumor
 * class of disease
 * intestinal benign neoplasm gastrointestinal neuroendocrine benign tumor
 * Human disease
 * DOID:4119
 * intestinal perforation
 * class of disease
 * intestinal disease gastrointestinal perforation
 * Human disease
 * DOID:2074
 * C06.405.469.557
 * intestinal tuberculosis
 * class of disease
 * gastrointestinal tuberculosis intestinal disease
 * human disease
 * DOID:13282
 * intestinal variant cervical mucinous adenocarcinoma
 * class of disease
 * cervical mucinous adenocarcinoma intestinal type carcinoma
 * Human disease
 * DOID:8339
 * intestinal volvulus
 * class of disease
 * bowel obstruction disease
 * Human disease
 * DOID:8445
 * C06.405.469.531.568 C23.300.970.500
 * Volvulus
 * intestine carcinoma in situ
 * class of disease
 * carcinoma in situ of digestive organ in situ carcinoma intestinal disease
 * Human disease
 * DOID:9024
 * intra-abdominal lymph node mast cell malignancy
 * class of disease
 * lymph node cancer mast cell malignancy of lymph nodes mastocytoma
 * Human disease
 * DOID:13005
 * intracerebral cystic meningioma
 * class of disease
 * cerebral meningioma
 * Human disease
 * DOID:6113
 * intracortical osteogenic sarcoma
 * class of disease
 * conventional central osteosarcoma
 * Human disease
 * DOID:7602
 * intracranial abscess
 * class of disease
 * central nervous system disease abscess
 * central nervous system disease that is located in the skull and is characterized by a collection of pus (infected material) inside the skull
 * DOID:10095
 * intracranial aneurysm
 * class of disease
 * aneurysm cerebrovascular disease cerebral arterial disease disease
 * cerebrovascular disorder
 * DOID:10941
 * C10.228.140.300.510.600 C14.907.055.635 C14.907.253.560.300
 * Cerebral aneurysms
 * Aneurysem.jpg
 * intracranial arterial disease
 * class of disease
 * cerebrovascular disease
 * human disease
 * DOID:13089
 * C10.228.140.300.510 C14.907.253.560
 * intracranial arteriosclerosis
 * class of disease
 * arteriosclerosis
 * human disease
 * DOID:13097
 * C10.228.140.300.510.800 C14.907.137.126.372 C14.907.253.560.350
 * intracranial berry aneurysm
 * class of disease
 * intracranial aneurysm
 * intracranial aneurysm with a characteristic rounded shape; the most common form of cerebral aneurysm
 * DOID:0060228
 * intracranial berry aneurysm 11
 * class of disease
 * intracranial berry aneurysm
 * human disease
 * DOID:0080974
 * intracranial berry aneurysm 9
 * class of disease
 * intracranial berry aneurysm
 * human disease
 * DOID:0080972
 * intracranial cavernous angioma
 * class of disease
 * intracranial structure hemangioma
 * Human disease
 * DOID:2516
 * intracranial chondrosarcoma
 * class of disease
 * extraosseous chondrosarcoma extraskeletal myxoid chondrosarcoma intracranial tumor
 * Human disease
 * DOID:7903
 * intracranial embolism
 * class of disease
 * cerebrovascular disease disease
 * Human disease
 * DOID:4372
 * C10.228.140.300.525.400 C14.907.253.566.300 C14.907.355.590.213.300
 * Intracranial embolism
 * intracranial liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5714
 * intracranial primitive neuroectodermal tumor
 * class of disease
 * central nervous system primitive neuroectodermal neoplasm medulloblastoma
 * Human disease
 * DOID:4788
 * intracranial structure hemangioma
 * class of disease
 * hemangioma intracranial tumor
 * Human disease
 * DOID:2517
 * intracranial thrombosis
 * class of disease
 * thrombosis cerebrovascular disease thromboembolism
 * Human disease
 * DOID:4193
 * C10.228.140.300.525.425 C14.907.253.566.350 C14.907.355.590.213.350
 * intracranial vasospasm
 * class of disease
 * vasospasm cerebrovascular disease disease
 * Human disease
 * DOID:13100
 * C10.228.140.300.900 C14.907.253.951
 * intracystic papillary adenoma
 * class of disease
 * adenoma
 * Human disease
 * DOID:2682
 * intraductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:8068
 * intraductal breast neoplasm
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:3013
 * intraductal carcinoma
 * class of disease
 * breast carcinoma in situ breast ductal carcinoma disease
 * Human disease
 * DOID:0060074
 * C04.557.470.200.025.275 C04.557.470.200.240.187.250 C04.557.470.615.275
 * Ductal carcinoma in situ
 * Breast DCIS histopathology (1).jpg
 * intraductal papillary breast neoplasm
 * class of disease
 * intraductal breast neoplasm
 * Human disease
 * DOID:1628
 * intraductal papilloma
 * class of disease
 * breast benign neoplasm papilloma intraductal breast neoplasm disease
 * human disease
 * DOID:1627
 * C04.557.470.615.670
 * Intraductal papilloma
 * intrahepatic bile duct adenoma
 * class of disease
 * bile duct adenoma
 * Human disease
 * DOID:5437
 * intrahepatic bile duct cystadenoma
 * class of disease
 * bile duct cystadenoma intrahepatic bile duct adenoma
 * Human disease
 * DOID:6733
 * intrahepatic biliary papillomatosis
 * class of disease
 * biliary papillomatosis
 * Human disease
 * DOID:8230
 * intrahepatic cholangiocarcinoma
 * class of disease
 * cholangiocarcinoma
 * Human disease
 * DOID:4928
 * intrahepatic cholestasis
 * class of disease
 * cholestasis
 * medical condition
 * DOID:1852
 * C06.130.120.135.250 C06.552.150
 * intrahepatic cholestasis of pregnancy
 * class of disease
 * intrahepatic cholestasis liver disease of pregnancy disease
 * intrahepatic cholestasis characterized by reversible cholestasis typically occurring in the second or third trimester of pregnancy, elevated serum aminotransferases and bile acid level and resolution of symptoms by 2 to 3 weeks after delivery
 * DOID:0070227
 * Cholestasis high mag.jpg
 * intrahepatic gall duct cancer
 * class of disease
 * gallbladder cancer
 * Human disease
 * DOID:12298
 * intramuscular hemangioma
 * class of disease
 * hemangioma muscle neoplasm
 * Human disease
 * DOID:468
 * intraneural perineurioma
 * class of disease
 * perineurioma
 * Human disease
 * DOID:4696
 * intraocular lymphoma
 * class of disease
 * eye lymphoma
 * human disease
 * DOID:775
 * C04.557.386.435 C04.588.364.447 C15.604.515.569.417 C20.683.515.761.417
 * intraorbital meningioma
 * class of disease
 * orbital cancer meningioma
 * meningioma by site and orbital neoplasm that is located in the area around the eye sockets of the skull and results in pressure in the eyes, giving a bulging appearance
 * DOID:4141
 * intrapelvic lymph node leukemic reticuloendotheliosis
 * class of disease
 * lymph node cancer
 * Human disease
 * DOID:12972
 * intratubular embryonal carcinoma
 * class of disease
 * embryonal testis carcinoma
 * embryonal testis carcinoma that is located within a tubule
 * DOID:8275
 * intravascular angioleiomyoma
 * class of disease
 * angiomyoma vascular neoplasm
 * Human disease
 * DOID:4266
 * intravascular fasciitis
 * class of disease
 * pseudosarcomatous fibromatosis
 * Human disease
 * DOID:9603
 * intravenous leiomyomatosis
 * class of disease
 * leiomyomatosis vascular disease
 * Human disease
 * DOID:5729
 * intraventricular meningioma
 * class of disease
 * cerebral ventricle cancer meningioma
 * Human disease
 * DOID:3772
 * intrinsic asthma
 * class of disease
 * asthma chronic asthma
 * human disease
 * DOID:9360
 * intussusception
 * class of disease
 * bowel obstruction genetic disease disease
 * human disease
 * DOID:8446
 * C06.405.469.531.577
 * Intussusception
 * VolvulusCT.PNG
 * invasive bladder transitional cell carcinoma
 * class of disease
 * bladder urothelial carcinoma Invasive urothelial carcinoma
 * Human disease
 * DOID:6477
 * invasive lobular carcinoma
 * class of disease
 * breast lobular carcinoma invasive breast carcinoma carcinoma breast cancer disease
 * Human disease
 * DOID:3457
 * Histopathology of invasive lobular carcinoma (ILC)
 * invasive malignant thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:3283
 * invasive tubular breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive ductal carcinoma
 * Human disease
 * DOID:6587
 * inverted follicular keratosis
 * class of disease
 * seborrheic keratosis
 * Human disease
 * DOID:6945
 * Inverted follicular keratosis
 * inverted papilloma
 * class of disease
 * papilloma
 * Human disease
 * DOID:3179
 * C04.557.470.700.600.610
 * Inverted papillomas
 * inverted transitional papilloma
 * class of disease
 * transitional papilloma inverted papilloma
 * Human disease
 * DOID:4630
 * iodine hypothyroidism
 * class of disease
 * hypothyroidism
 * Human disease
 * DOID:5083
 * iris cancer
 * class of disease
 * iris neoplasm uveal cancer iris disease
 * Human disease
 * DOID:3478
 * iris disease
 * class of disease
 * uveal disease
 * Human disease
 * DOID:240 DOID:4738
 * C11.941.375
 * iritis
 * class of disease
 * iris disease anterior uveitis disease
 * human disease
 * DOID:1406
 * C11.941.375.385 C11.941.879.780.880.448
 * iron deficiency anemia
 * class of disease symptom or sign
 * deficiency anemia nutritional deficiency disease iron deficiency hypochromic anemia disease
 * anemia caused by a lack of iron
 * DOID:11758
 * C15.378.071.196.300 C18.452.565.100
 * Iron-deficiency anemia
 * Heme b.svg
 * iron metabolism disease
 * class of disease
 * mineral metabolism disease
 * Human disease
 * DOID:2351
 * C18.452.565
 * irregular astigmatism
 * class of disease
 * astigmatism
 * Human disease
 * DOID:13919
 * irritable bowel syndrome
 * class of disease symptom or sign
 * functional colonic disease syndrome intestinal disease disease
 * syndrome that is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause
 * DOID:9778
 * C06.405.469.158.272.608
 * Irritable bowel syndrome
 * Irritable bowel syndrome.jpg
 * irritant dermatitis
 * class of disease
 * contact dermatitis
 * human disease
 * DOID:2772
 * C17.800.174.255.400 C17.800.815.255.400
 * Irritant contact dermatitis
 * ischemic bone disease
 * class of disease
 * bone disease ischemia
 * bone disease that results in an interruption of blood supply located in bone
 * DOID:0080008
 * ischemic colitis
 * class of disease
 * colitis
 * colitis caused by inadequate blood supply to the colon
 * DOID:0060181
 * C06.405.205.265.115 C06.405.469.158.188.115 C14.907.286
 * Ischemic colitis
 * ischemic fasciitis
 * class of disease
 * fasciitis
 * human disease
 * DOID:9601
 * Ischemic fasciitis
 * ischemic neuropathy
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:1195
 * islet cell carcinoma
 * class of disease
 * islet cell tumor gastrointestinal carcinoma disease
 * islet cell tumor that has material basis in epithelial cells
 * DOID:1798
 * C04.557.470.200.025.290 C04.588.274.761.500 C04.588.322.475.500 C06.301.761.500 C06.689.667.500 C19.344.421.500
 * Pancreatic neuroendocrine tumors
 * islet cell tumor
 * class of disease
 * pancreatic cancer
 * pancreatic cancer that is located in the pancreatic islet cells
 * DOID:1799
 * isocyanates allergic asthma
 * class of disease
 * allergic asthma occupational asthma
 * allergic asthma that has allergic trigger isocyanates
 * DOID:0040041
 * isolated cryptophthalmia
 * class of disease
 * cryptophthalmos
 * human disease
 * DOID:0111717
 * isolated ectopia lentis
 * class of disease
 * lens disease ectopia lentis
 * A lens disease characterized by abnormal stretching of the zonular fibers resulting in dislocation of the lens. This dislocation may be mild to severe and may progress with age.
 * DOID:0111148
 * isolated growth hormone deficiency type IA
 * class of disease
 * isolated growth hormone deficiency
 * human disease
 * DOID:0060873
 * isolated growth hormone deficiency type IB
 * class of disease
 * isolated growth hormone deficiency
 * human disease
 * DOID:0060874
 * isolated growth hormone deficiency type II
 * class of disease
 * isolated growth hormone deficiency
 * human disease
 * DOID:0060872
 * isolated growth hormone deficiency type III
 * class of disease
 * isolated growth hormone deficiency X-linked recessive disease
 * An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material basis in mutation in the BTK gene on chromosome Xq22.1.
 * DOID:0060875
 * isolated microphthalmia
 * class of disease
 * microphthalmia
 * microphthalmia that is not part of a larger syndrome
 * DOID:0080637
 * isolated microphthalmia 1
 * class of disease
 * microphthalmia genetic disease isolated microphthalmia autosomal recessive disease
 * microphthalmia that has material basis in variation in the chromosomal region 14q32
 * DOID:0060840
 * isoniazide allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger isoniazide
 * DOID:0040008
 * isthmicoma
 * class of disease
 * hair follicle neoplasm
 * Human disease
 * DOID:8426
 * Isthmicoma
 * isthmus cancer
 * class of disease
 * uterine corpus cancer
 * Human disease
 * DOID:9459
 * jaw cancer
 * class of disease
 * bone cancer neoplasm of jaw
 * bone cancer and jaw disease that is located in the jaw and results in a swollen jaw, results in numbness or a tingling sensation in jaw, and results in an abnormal growth of the jaw bone
 * DOID:1862
 * jaw-winking syndrome
 * class of disease
 * cranial nerve disease ptosis genetic peripheral neuropathy
 * autosomal dominant condition with incomplete penetrance, in which nursing infants will have rhythmic upward jerking of their upper eyelid
 * DOID:560
 * Marcus Gunn phenomenon
 * jejunal adenocarcinoma
 * class of disease
 * jejunal cancer adenocarcinoma
 * jejunal cancer that is located in the jejunum and has material basis in epithelial tissue that has glandular origin
 * DOID:0050926
 * jejunal cancer
 * class of disease
 * small intestine cancer jejunal neoplasm
 * human disease
 * DOID:13499
 * jejunal neoplasm
 * class of disease
 * small intestine neoplasm jejunal disease
 * human disease
 * DOID:3218
 * C04.588.274.476.411.523 C06.301.371.411.523 C06.405.249.411.523 C06.405.469.491.523 C06.405.469.600.523
 * jejunal somatostatinoma
 * class of disease
 * jejunal cancer
 * Human disease
 * DOID:3216
 * junctional epidermolysis bullosa Herlitz type
 * class of disease
 * junctional epidermolysis bullosa genetic disease autosomal recessive disease
 * Human disease
 * DOID:0060737
 * juvenile absence epilepsy
 * class of disease
 * adolescence-adult electroclinical syndrome
 * adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures
 * DOID:0060172
 * juvenile absence epilepsy 1
 * class of disease
 * juvenile absence epilepsy
 * human disease
 * DOID:0111324
 * juvenile amyotrophic lateral sclerosis with dementia
 * class of disease
 * amyotrophic lateral sclerosis juvenile amyotrophic lateral sclerosis
 * juvenile amyotrophic lateral sclerosis that is slowly progressive with concomitantly progressive dementia
 * DOID:0110067
 * juvenile ankylosing spondylitis
 * class of disease
 * autoimmune disease of musculoskeletal system ankylosing spondylitis
 * autoimmune disease of musculoskeletal system that is an ankylosing spondylitis with onset during childhood
 * DOID:0040092
 * juvenile astrocytoma
 * class of disease
 * astrocytoma childhood cancer
 * Human disease
 * DOID:3079
 * juvenile dermatitis herpetiformis
 * class of disease
 * dermatitis herpetiformis
 * Human disease
 * DOID:8507
 * juvenile glaucoma
 * class of disease
 * autosomal dominant disease primary open angle glaucoma
 * Human disease
 * DOID:1068
 * juvenile myelomonocytic leukemia
 * class of disease
 * myelodysplastic/myeloproliferative neoplasm monocytic leukemia childhood leukemia
 * Human disease
 * DOID:0050458
 * C04.557.337.539.525 C15.378.190.615.520
 * juvenile myoclonic epilepsy
 * class of disease
 * adolescence-adult electroclinical syndrome Idiopathic generalized epilepsy myoclonic epilepsy
 * adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years
 * DOID:4890
 * C10.228.140.490.493.063.670 C10.228.140.490.375.130.670
 * juvenile myoclonic epilepsy 10
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111325
 * juvenile myoclonic epilepsy 3
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111326
 * juvenile myoclonic epilepsy 4
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111327
 * juvenile myoclonic epilepsy 9
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111328
 * juvenile pilocytic astrocytoma
 * class of disease
 * childhood pilocytic astrocytoma pilocytic astrocytoma
 * Human disease
 * DOID:6811
 * juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
 * class of disease
 * autosomal dominant disease syndrome juvenile polyposis syndrome hereditary hemorrhagic telangiectasia
 * human disease
 * DOID:0111543
 * juvenile type testicular granulosa cell tumor
 * class of disease
 * testicular granulosa cell tumor
 * Human disease
 * DOID:6032
 * juvenile xanthogranuloma
 * class of disease
 * non-Langerhans-cell histiocytosis histiocytosis xanthogranuloma
 * Human disease
 * DOID:4424
 * C15.604.250.410.900 C17.800.973
 * Juvenile xanthogranuloma
 * juvenile-onset Parkinson disease
 * class of disease
 * Parkinson's disease young-onset Parkinson disease
 * human disease
 * DOID:0060893
 * juxtacortical chondroma
 * class of disease
 * chondroma
 * Human disease
 * DOID:2601
 * juxtacortical chondrosarcoma
 * class of disease
 * chondrosarcoma
 * human disease
 * DOID:5866
 * juxtacortical osteosarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:3373
 * C04.557.450.565.575.650.655 C04.557.450.795.620.655
 * keratinizing squamous cell carcinoma
 * class of disease
 * squamous cell carcinoma
 * squamous cell carcinoma that presents as single, isolated cells with bizzare cytoplasmic shapes, intense cytoplasmic eosinophilia, and intensely hyperchromatic, angular nuclei in a background of necrotic and keratinous debris
 * DOID:5521
 * keratitis
 * class of disease symptom or sign
 * corneal disease eye inflammation inflammatory disease cornea symptom disease
 * corneal disease that is characterized by inflammation of the cornea.
 * DOID:4677
 * C11.204.564
 * Keratitis
 * Clare-314.jpg
 * keratoacanthoma
 * class of disease
 * cutaneous squamous-cell carcinoma disease
 * Human disease
 * DOID:3149
 * C17.800.417
 * Keratoacanthoma
 * Keratoacanthoma 2.jpg
 * keratoconjunctivitis
 * class of disease
 * keratitis conjunctivitis eye disease
 * inflammation ("-itis") of the cornea and conjunctiva.
 * DOID:9368
 * C11.187.183.394 C11.204.564.585
 * Keratoconjunctivitis
 * Gade corneyo-djontivite clamidia3.jpg
 * keratoconjunctivitis sicca
 * class of disease
 * dry eye syndrome keratoconjunctivitis disease
 * condition of having dry eyes
 * DOID:12895
 * C11.187.183.394.550 C11.204.564.585.630 C11.496.260.394
 * Dry eye syndrome
 * keratomalacia
 * class of disease
 * corneal degeneration vitamin A deficiency keratitis related to vitamin deficiency disease
 * Human disease
 * DOID:11267
 * keratopathy
 * class of disease
 * corneal disease
 * Human disease
 * DOID:2283
 * keratosis
 * class of disease
 * skin disease keratoma disease
 * skin disease characterized by growth of keratin on the skin or mucous membranes
 * DOID:161
 * C17.800.428
 * Keratosis pilaris arm.jpg
 * keratosis follicularis spinulosa decalvans, autosomal dominant
 * class of disease
 * keratosis follicularis spinulosa decalvans
 * human disease
 * DOID:0080755
 * keratosis pilaris atrophicans faciei
 * class of disease
 * keratosis pilaris atropicans
 * human disease
 * DOID:0080752
 * keratosis pilaris atropicans
 * class of disease
 * keratosis pilaris autosomal recessive disease ichthyosis
 * human disease
 * DOID:0080751
 * kernicterus
 * class of disease symptom or sign
 * encephalopathy neurometabolic disease neonatal jaundice disease
 * congenital disorder of nervous system
 * DOID:2382
 * C10.228.140.163.480 C15.378.295.502 C16.614.304.502 C18.452.132.480 C20.306.502 C23.550.429.750
 * Kernicterus
 * kernicterus due to isoimmunization
 * class of disease
 * neonatal jaundice kernicterus
 * Human disease
 * DOID:12043
 * ketoprofen photoallergic dermatitis
 * class of disease
 * photodermatitis drug allergy
 * photoallergic dermatitis that has allergic trigger ketoprofen
 * DOID:0040060
 * kidney angiomyolipoma
 * class of disease
 * kidney benign neoplasm angiomyolipoma benign perivascular tumor
 * angiomyolipoma arising from the kidney
 * DOID:8411
 * Renal angiomyolipoma
 * kidney benign neoplasm
 * class of disease
 * urinary system benign neoplasm kidney neoplasm kidney disease lipoma
 * A non-metastasizing neoplasm that arises from the kidney. Representative examples include cystic nephroma, metanephric adenoma, oncocytoma, and urothelial papilloma of the renal pelvis.
 * DOID:3116
 * kidney cancer
 * class of disease
 * urinary system cancer kidney neoplasm kidney disease disease
 * urinary system cancer that is located in the kidney
 * DOID:263
 * Cancers of kidney
 * kidney carcinoma in situ
 * class of disease
 * kidney disease in situ carcinoma
 * Human disease
 * DOID:9234
 * kidney clear cell sarcoma
 * class of disease
 * kidney cancer kidney sarcoma inherited renal tumor clear-cell sarcoma
 * kidney sarcoma that has material basis in clear cells that are characterized as cells that look clear when viewed under a microscope
 * DOID:4880
 * kidney cortex disease
 * class of disease
 * kidney disease
 * human disease
 * DOID:0080616
 * kidney failure
 * class of disease symptom or sign
 * kidney disease impaired renal function disease chronic renal disease urological symptom disease
 * disease where the kidneys fail to adequately filter waste products from the blood
 * DOID:1074
 * C12.777.419.780 C13.351.968.419.780
 * kidney fibrosarcoma
 * class of disease
 * kidney sarcoma fibrosarcoma
 * Human disease
 * DOID:5982
 * kidney hemangiopericytoma
 * class of disease
 * kidney cancer
 * kidney cancer which is manifested in the kidney
 * DOID:262
 * kidney hypertrophy
 * class of disease
 * kidney disease
 * Global enlargement of the renal parenchyma in one or both kidneys
 * DOID:9622
 * kidney infection
 * class of disease
 * infection kidney disease infectious disease
 * type of infection that afflicts the kidneys
 * DOID:782
 * kidney leiomyosarcoma
 * class of disease
 * kidney sarcoma
 * leiomyosarcoma and sarcoma of kidney that is located in the kidney
 * DOID:5287
 * kidney lipoma
 * class of disease
 * kidney benign neoplasm
 * Human disease
 * DOID:10194
 * kidney liposarcoma
 * class of disease
 * liposarcoma kidney sarcoma kidney cancer
 * liposarcoma that is located in the kidney
 * DOID:5699
 * kidney osteogenic sarcoma
 * class of disease
 * kidney sarcoma extraosseous osteosarcoma
 * kidney sarcoma that starts in the bones and that is located in the kidney
 * DOID:5983
 * kidney papillary necrosis
 * class of disease
 * kidney disease disease
 * Human disease
 * DOID:2981
 * C12.777.419.493 C13.351.968.419.493
 * kidney pelvis papillary carcinoma
 * class of disease
 * renal pelvis transitional cell carcinoma renal pelvis papillary tumor papillary transitional carcinoma
 * Human disease
 * DOID:5973
 * kidney pelvis sarcomatoid transitional cell carcinoma
 * class of disease
 * sarcomatoid transitional cell carcinoma transitional cell carcinoma renal pelvis carcinoma
 * Human disease
 * DOID:6844
 * kidney rhabdoid cancer
 * class of disease
 * rhabdoid tumor kidney sarcoma
 * embryonal cancer that is located in the kidney
 * DOID:3674
 * kidney sarcoma
 * class of disease
 * kidney cancer sarcoma
 * kidney cancer that is located in the kidney&#39;s connective tissue
 * DOID:4242
 * klebsiellosis
 * class of disease
 * bacterial pneumonia Enterobacteriaceae infectious disease
 * infection by Klebsiella bacteria
 * DOID:13272
 * C01.150.252.400.310.503
 * kleptomania
 * class of disease
 * impulse control disorder disease
 * inability to resist the urge to steal
 * DOID:12400
 * Kleptomania
 * Constant Wauters Der ertappte Hausdiener.jpg
 * kwashiorkor
 * class of disease
 * protein-energy malnutrition disease dystrophy protein deficiency
 * Human disease
 * DOID:13579
 * C18.654.521.719.500
 * Kwashiorkor
 * Kwashiorkor 6180.jpg
 * kyphoscoliotic heart disease
 * class of disease
 * chronic pulmonary heart disease
 * Human disease
 * DOID:12325
 * labia majora carcinoma
 * class of disease
 * vulva carcinoma skin cancer
 * Human disease
 * DOID:13389
 * labia minora cancer
 * class of disease
 * vulvar cancer skin cancer
 * Human disease
 * DOID:1243
 * labia minora carcinoma
 * class of disease
 * vulva carcinoma
 * Human disease
 * DOID:1293
 * labium majus cancer
 * class of disease
 * vulvar cancer
 * Human disease
 * DOID:11905
 * labyrinthine bilateral reactive loss
 * class of disease
 * labyrinthine dysfunction
 * Human disease
 * DOID:14413
 * labyrinthine unilateral reactive loss
 * class of disease
 * labyrinthine dysfunction
 * Human disease
 * DOID:1776
 * labyrinthitis
 * class of disease
 * otitis interna inner ear disease labyrinthosis disease
 * inflammation of the labyrinth, fluid-filled channels in the inner ear
 * DOID:1468
 * C09.218.568.558 C09.218.705.371
 * lacrimal apparatus disease
 * class of disease
 * eye disease eye adnexa disease rare palpebral, lacrimal system and conjunctival disease rare genetic palpebral, lacrimal system and conjunctival disease
 * human disease
 * DOID:1400
 * C11.496
 * lacrimal duct cancer
 * class of disease
 * lacrimal system cancer
 * Human disease
 * DOID:12756
 * lacrimal duct obstruction
 * class of disease
 * lacrimal apparatus disease stenosis and insufficiency of lacrimal passage
 * Human disease
 * DOID:13929
 * C11.496.456
 * Nasolacrimal duct obstruction
 * Tear system.svg
 * lacrimal gland adenocarcinoma
 * class of disease
 * lacrimal gland carcinoma adenocarcinoma
 * human disease
 * DOID:298
 * lacrimal gland cancer
 * class of disease
 * lacrimal system cancer lacrimal gland neoplasm
 * human disease
 * DOID:294
 * lacrimal gland carcinoma
 * class of disease
 * lacrimal gland cancer carcinoma
 * Human disease
 * DOID:293
 * lacrimal passage granuloma
 * class of disease
 * lacrimal apparatus disease
 * Human disease
 * DOID:10174
 * lacrimal system cancer
 * class of disease
 * ocular cancer lacrimal apparatus disease
 * human disease
 * DOID:292
 * lactic acidosis
 * class of disease
 * acidosis metabolic acidosis disease
 * acquired metabolic condition that has material basis in low pH in body tissues and blood accompanied by the buildup of lactate especially D-lactate
 * DOID:3650
 * C18.452.076.176.180
 * Lactic acidosis
 * lactose intolerance
 * class of disease
 * carbohydrate metabolic disorder malabsorption food intolerance disease
 * condition involving a decreased ability to digest lactose due to a lack of lactase in the small intestines, either genetically or from injury
 * DOID:10604
 * C06.405.469.637.506 C16.320.565.202.589 C18.452.603.506 C18.452.648.202.589
 * Lactose intolerance
 * Lactose(lac).png
 * lambda 5 deficiency
 * class of disease
 * B cell deficiency genetic disease monogenic disease
 * A B cell deficiency that has material basis in mutations in the IGLL1 gene. Lambda 5 mutations an cause a block in B cell development at the transition between the pro-B cell and the pre-B cell stage.
 * DOID:0060024
 * language disorder
 * class of disease
 * communication disorder
 * range of neurodevelopmental conditions
 * DOID:93
 * C10.597.606.150.500 C23.888.592.604.150.500
 * large bowel leiomyoma
 * class of disease
 * intestinal benign neoplasm leiomyoma benign neoplasm of large intestine
 * Human disease
 * DOID:5143
 * large cell carcinoma
 * class of disease
 * carcinoma
 * carcinoma that is composed of large, monotonous rounded or overtly polygonal-shaped cells with abundant cytoplasm
 * DOID:4552
 * C04.557.470.200.260
 * large cell carcinoma with rhabdoid phenotype
 * class of disease
 * large-cell lung carcinoma
 * Human disease
 * DOID:7480
 * large cell keratinizing variant squamous cell breast carcinoma
 * class of disease
 * breast squamous cell carcinoma keratinizing squamous cell carcinoma
 * Human disease
 * DOID:7461
 * large cell medulloblastoma
 * class of disease
 * medulloblastoma
 * medulloblastoma that is characterized by cells that are larger than would be normally expected
 * DOID:3857
 * large cell neuroendocrine carcinoma
 * class of disease
 * large cell carcinoma neuroendocrine carcinoma large-cell lung carcinoma
 * Human disease
 * DOID:0050872
 * Large cell neuroendocrine carcinoma
 * large cell neuroendocrine carcinoma of the lung
 * class of disease
 * large cell neuroendocrine carcinoma large-cell lung carcinoma pulmonary neuroendocrine tumor
 * human disease
 * DOID:6658
 * large intestine adenocarcinoma
 * class of disease
 * large intestine cancer adenocarcinoma
 * large intestine cancer that has material basis in epithelial cells of glandular origin
 * DOID:0050913
 * large intestine adenoma
 * class of disease
 * intestinal benign neoplasm gastrointestinal adenoma benign neoplasms by histologic type
 * intestinal benign neoplasm that has material basis in epithelial tissue with glandular origin and is located in the large intestine
 * DOID:0050914
 * large intestine cancer
 * class of disease
 * intestinal cancer colorectal neoplasm
 * intestinal cancer that effects the long, tube-like organ that is connected to the small intestine at one end and the anus at the other
 * DOID:5672
 * large intestine lipoma
 * class of disease
 * intestinal benign neoplasm lipoma benign neoplasm of large intestine
 * Human disease
 * DOID:6460
 * large-cell acanthoma
 * class of disease
 * acanthoma
 * Human disease
 * DOID:4321
 * large-cell lung carcinoma
 * class of disease
 * non-small-cell lung carcinoma large cell carcinoma disease
 * Disease
 * DOID:4556
 * Large-cell lung carcinoma
 * large-cell lymphoma
 * class of disease
 * lymphatic system cancer non-Hodgkin lymphoma
 * Human disease
 * DOID:8538
 * laryngeal adenoid cystic carcinoma
 * class of disease
 * laryngeal carcinoma
 * Human disease
 * DOID:4869
 * laryngeal cancer
 * class of disease
 * head and neck cancer carcinoma laryngeal neoplasm respiratory system cancer disease
 * respiratory system cancer that is located in the larynx
 * DOID:2596
 * Laryngeal cancer
 * Tumor Laryngis-01.jpg
 * laryngeal carcinoma
 * class of disease
 * laryngeal cancer carcinoma
 * larynx cancer that has material basis in epithelial cells
 * DOID:2600
 * laryngeal cartilage cancer
 * class of disease
 * laryngeal cancer
 * Human disease
 * DOID:13348
 * laryngeal disease
 * class of disease
 * upper respiratory tract disease
 * human disease
 * DOID:786
 * C08.360 C09.400
 * laryngeal mucoepidermoid carcinoma
 * class of disease
 * mucoepidermoid carcinoma laryngeal cancer
 * Human disease
 * DOID:4688
 * laryngeal neoplasm
 * class of disease
 * respiratory tract neoplasm laryngeal disease neoplasm respiratory system benign neoplasm
 * human disease
 * DOID:2598
 * C04.588.443.665.481 C08.360.369 C08.785.481 C09.400.369 C09.647.481
 * Neoplasms of larynx
 * laryngitis
 * class of disease symptom or sign
 * laryngeal disease inflammatory disease throat symptom disease
 * inflammation of the larynx
 * DOID:3437
 * C08.360.535 C08.730.368 C09.400.535 C01.748.368
 * Laryngitis
 * Laryngitis gastrica.jpg
 * laryngostenosis
 * class of disease
 * laryngeal disease
 * Human disease
 * DOID:11527
 * C08.360.591 C09.400.591 C16.131.740.658
 * laryngotracheitis
 * class of disease symptom or sign
 * upper respiratory tract disease throat symptom
 * human disease
 * DOID:0050148
 * larynx carcinoma in situ
 * class of disease
 * laryngeal disease in situ carcinoma
 * Human disease
 * DOID:9011
 * larynx leiomyoma
 * class of disease
 * laryngeal neoplasm leiomyoma
 * Human disease
 * DOID:10070
 * larynx leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * larynx sarcoma that is a smooth muscle connective tissue tymor located in the larynx
 * DOID:5288
 * larynx liposarcoma
 * class of disease
 * liposarcoma laryngeal cancer
 * liposarcoma that is located in the larynx
 * DOID:5696
 * larynx sarcoma
 * class of disease
 * laryngeal cancer sarcoma
 * larynx cancer that has material basis in abnormally proliferating cells derived from embryonic mesoderm
 * DOID:2877
 * larynx squamous papilloma
 * class of disease
 * laryngeal neoplasm squamous cell papilloma laryngeal papillomatosis
 * Human disease
 * DOID:10071
 * late congenital syphilis
 * class of disease
 * congenital syphilis
 * Human disease
 * DOID:10039
 * late yaws
 * class of disease
 * yaws
 * yaws that appears after five years of the initial infection and is characterized by disabling consequences of the nose, bones and palmar/plantar hyperkeratosis
 * DOID:10567
 * late-adult onset retinitis pigmentosa
 * class of disease
 * retinitis pigmentosa autosomal recessive disease
 * retinitis pigmentosa that is characterized by onset of symptoms in the fifth or sixth decade of life
 * DOID:0110421
 * lateral cystocele
 * class of disease
 * pelvic organ prolapse cystocele
 * Human disease
 * DOID:14130
 * lateral displacement of eye
 * class of disease
 * orbital disease exophthalmos
 * Human disease
 * DOID:12360
 * lateral medullary syndrome
 * class of disease
 * brain stem infarction
 * neurological disorder causing a range of symptoms due to ischemia in the lateral part of the medulla oblongata in the brainstem
 * DOID:3522
 * C10.228.140.300.150.477.100.500 C10.228.140.300.775.200.100.500 C14.907.253.092.477.100.500 C14.907.253.855.200.100.500 C23.550.513.355.250.100.500 C23.550.717.489.250.100.500
 * Lateral medullary syndrome
 * WallenbergInfarct001.jpg
 * lateral myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5853
 * lateral sinus thrombosis
 * class of disease
 * cerebral venous sinus thrombosis
 * Human disease
 * DOID:3574
 * C10.228.140.300.525.425.500.562 C14.907.253.566.350.500.562 C14.907.355.590.213.350.500.562
 * lateral ventricle meningioma
 * class of disease
 * intraventricular meningioma cerebral meningioma cerebral ventricle cancer
 * Human disease
 * DOID:6115
 * latex allergy
 * class of disease
 * allergy hazard disease
 * hypersensitivity reaction type I disease triggered by latex
 * DOID:0060532
 * C20.543.600
 * learning disability
 * class of disease
 * specific developmental disorder disability disease
 * range of neurodevelopmental conditions
 * DOID:8927
 * C10.597.606.150.550 C23.888.592.604.150.550 F03.625.562 F03.625.374.188
 * Learning disabilities
 * leech infestation
 * class of disease
 * ectoparasitism disease
 * human disease
 * DOID:11079
 * leg dermatosis
 * class of disease
 * skin disease
 * Human disease
 * DOID:3142
 * C17.800.446
 * legionellosis
 * class of disease
 * primary bacterial infectious disease
 * Human disease
 * DOID:10458
 * C01.150.252.400.500 C08.730.382 C01.748.382
 * legume allergy
 * class of disease
 * fruit allergy
 * human disease
 * DOID:0060904
 * leiomyoma
 * class of disease
 * benign neoplasms by histologic type smooth muscle tumour myoma disease
 * cell type benign neoplasm that is a benign tumor of smooth muscle cells
 * DOID:127
 * C04.557.450.590.450
 * Leiomyomas
 * Leiomyoma Uterus 40x.jpg
 * leiomyoma cutis
 * class of disease
 * dermis tumor skin benign neoplasm leiomyoma
 * benign tumor that arises from smooth muscle tissue in a hair follicle, forming a papule
 * DOID:5132
 * Cutaneous leiomyoma
 * leiomyomatosis
 * class of disease
 * leiomyoma
 * Human disease
 * DOID:5138
 * C04.557.450.590.450.465
 * leiomyosarcoma
 * class of disease
 * smooth muscle cancer disease
 * malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis
 * DOID:1967
 * C04.557.450.590.455 C04.557.450.795.455
 * Leiomyosarcoma
 * Cutaneous leiomyosarcoma - high mag.jpg
 * lens disease
 * class of disease
 * eye disease
 * Human disease
 * DOID:110
 * C11.510
 * lens subluxation
 * class of disease
 * lens disease
 * Human disease
 * DOID:11364
 * C11.510.598
 * lens-induced iridocyclitis
 * class of disease
 * iridocyclitis
 * Human disease
 * DOID:9388
 * leptomeninges sarcoma
 * class of disease
 * malignant leptomeningeal tumor meninges sarcoma sarcoma
 * Human disease
 * DOID:7689
 * lesion of sciatic nerve
 * class of disease
 * mononeuritis of lower limb
 * Human disease
 * DOID:12528
 * lethal congenital contracture syndrome 1
 * class of disease
 * lethal congenital contracture syndrome genetic disease
 * lethal congenital contracture syndrome that has material basis in homozygous or compound heterozygous mutation in the mRNA export mediator GLE1 on chromosome 9q34
 * DOID:0060559
 * leucine-sensitive hypoglycemia of infancy
 * class of disease
 * amino acid metabolic disorder autosomal dominant disease
 * human disease
 * DOID:0112262
 * leukemia
 * class of disease symptom or sign
 * hematologic cancer myeloproliferative disorders disease
 * group of cancers that usually begin in the bone marrow
 * DOID:1240
 * C04.557.337
 * Leukemias
 * Symptoms of leukemia.png
 * leukocoria
 * class of disease
 * pupil disorder eye degenerative disease
 * abnormal white reflection from the retina of the eye
 * DOID:11772
 * Leukocoria
 * Rb whiteeye.PNG
 * leukocyte adhesion deficiency 2
 * class of disease
 * leukocyte adhesion deficiency 3
 * leukocyte adhesion deficiency that is characterized by recurrent bacterial infections, severe growth delay and severe intellectual deficit
 * DOID:0080492
 * leukocyte disease
 * class of disease symptom or sign
 * hematopoietic system disease
 * disease involving the leukocyte
 * DOID:9500
 * C15.378.553
 * Leukocyte disorders
 * leukodystrophy
 * class of disease
 * cerebral degeneration disease
 * cerebral degeneration characterized by dysfunction of the white matter of the brain
 * DOID:10579
 * Leukodystrophies
 * leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
 * class of disease
 * nervous system heredodegenerative disease combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111493
 * leukopenia
 * class of disease symptom or sign
 * leukocyte disease cytopenia hemic system symptom disease
 * decrease in the number of white blood cells
 * DOID:615
 * C15.378.553.546
 * leukoplakia of penis
 * class of disease
 * penile disease leukoplakia
 * Human disease
 * DOID:8738
 * leukoplakia of vagina
 * class of disease
 * vaginal disease leukoplakia
 * Human disease
 * DOID:8920
 * leukorrhea
 * class of disease
 * vaginal discharge disease
 * type of vaginal discharge
 * DOID:3766
 * C13.351.500.894.700.500
 * leukostasis
 * class of disease
 * leukocyte disease leukocytosis
 * human disease
 * DOID:12986
 * C15.378.553.560
 * lichen disease
 * class of disease
 * skin disease lichenoid eruption
 * Human disease
 * DOID:8574
 * lichen nitidus
 * class of disease
 * lichen disease
 * Human disease
 * DOID:8573
 * C17.800.859.475.545
 * Lichen nitidus
 * lichen planus
 * class of disease
 * lichen disease disease
 * chronic disease of skin, tongue or oral mucosa
 * DOID:9201
 * C17.800.859.475.560
 * Lichen planus
 * Lichen planus lip.jpg
 * lidocaine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger lidocaine
 * DOID:0040009
 * limb ischemia
 * class of disease
 * ischemia
 * Human disease
 * DOID:0050852
 * Limb ischemia
 * limb-girdle muscular dystrophy
 * class of disease
 * muscular dystrophy progressive muscular dystrophy disease
 * muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles
 * DOID:11724
 * C05.651.534.500.280 C10.668.491.175.500.149 C16.320.577.280
 * limbic encephalitis
 * class of disease
 * paraneoplastic neurologic syndrome encephalitis inflammatory and autoimmune disease with epilepsy autoimmune disease of the nervous system
 * Inflammation involving the limbic system in the brain
 * DOID:0080741
 * C04.588.614.550.450 C04.730.856.437 C10.228.140.430.525 C10.228.228.245.700 C10.574.781.550
 * limited scleroderma
 * class of disease
 * systemic scleroderma
 * the least progressive form of systemic scleroderma with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk
 * DOID:1577
 * C17.300.799.801 C17.800.784.801
 * linear skin defects with multiple congenital anomalies 1
 * class of disease
 * microphthalmia–dermal aplasia–sclerocornea syndrome X-linked dominant disease congenital disorder
 * human disease
 * DOID:0111808
 * lingual goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13196
 * C16.131.894.500.500 C19.874.283.802 C19.874.689.500.500
 * lingual-facial-buccal dyskinesia
 * class of disease
 * movement disorders
 * Human disease
 * DOID:9854
 * linitis plastica
 * class of disease
 * gastric diffuse adenocarcinoma stomach carcinoma disease
 * Human disease
 * DOID:4023
 * C04.557.470.200.025.095.410
 * Linitis plastica
 * lip disease
 * class of disease
 * mouth disease
 * human disease
 * DOID:9297
 * C07.465.409
 * Lip disorders
 * lipid metabolism disorder
 * class of disease
 * inherited metabolic disorder disease
 * high cholesterol & lipids
 * DOID:3146
 * C18.452.584
 * Dyslipidemia
 * Fig21Femme obese.jpg
 * lipid storage disease
 * class of disease
 * lysosomal storage disease disease
 * lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body&#39;s cells and tissues
 * DOID:9455
 * C16.320.565.398.641 C18.452.584.563.641 C18.452.648.398.641
 * Lipid storage disorders
 * lipid-cell variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:7967
 * lipid-rich breast carcinoma
 * class of disease
 * lipid-rich carcinoma bilateral breast cancer
 * lipid-rich carcinoma characterized by the presence of cytoplasmic neutral lipids in the vast majority of the malignant cells
 * DOID:7076
 * lipid-rich carcinoma
 * class of disease
 * breast carcinoma
 * breast carcinoma characterized by the presence of malignant epithelial cells with clear cytoplasm which contains neutral lipids
 * DOID:5658
 * lipoadenoma
 * class of disease
 * adenoma
 * adenoma that is composed of adipose tissue
 * DOID:5398
 * lipoatrophic diabetes
 * class of disease
 * type 2 diabetes
 * type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes
 * DOID:11712
 * C18.452.394.750.149.500 C19.246.300.500
 * lipoid nephrosis
 * class of disease
 * idiopathic nephrotic syndrome nephrotic syndrome disease
 * Human disease
 * DOID:10966
 * C12.777.419.630.477 C13.351.968.419.630.477
 * Minimal change disease
 * lipoma
 * class of disease
 * benign neoplasms by histologic type adipose tissue neoplasm disease
 * benign tumor made of fat tissue
 * DOID:3315
 * C04.557.450.550.400
 * Lipomas
 * Lipoma 02.jpg
 * lipoma of colon
 * class of disease
 * large intestine lipoma colonic disease
 * Human disease
 * DOID:10655
 * lipoma of spermatic cord
 * class of disease
 * paratesticular lipoma lipoma male reproductive organ benign neoplasm
 * Human disease
 * DOID:10206
 * lipoma of the rectum
 * class of disease
 * large intestine lipoma benign neoplasm of rectum
 * Human disease
 * DOID:6459
 * lipomatosis
 * class of disease
 * skin disease
 * Human disease
 * DOID:3153
 * C17.800.463 C18.452.584.718
 * Lipomatosis
 * liposarcoma
 * class of disease
 * lipomatous cancer sarcoma disease
 * lipomatous cancer that arises in fat cells in deep soft tissue retroperitoneum
 * DOID:3382
 * C04.557.450.550.420 C04.557.450.795.465
 * Liposarcoma
 * Myxoid liposarcoma (06).JPG
 * liposarcoma of bone
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3381
 * liposarcoma of the ovary
 * class of disease
 * ovary sarcoma liposarcoma sarcoma ovarian cancer
 * Human disease
 * DOID:5697
 * lissencephaly 3
 * class of disease
 * autosomal dominant disease lissencephaly
 * human disease
 * DOID:0112232
 * liver angiosarcoma
 * class of disease
 * angiosarcoma liver cancer hepatic vascular disease liver sarcoma organ type
 * angiosarcoma and sarcoma of liver and hemangioma of intra-abdominal structure and Ca liver - primary that is located in the liver
 * DOID:268
 * Liver angiosarcoma
 * Gross specimen of liver angiosarcoma.jpg
 * liver cancer
 * class of disease
 * liver tumor liver disease rare hepatic and biliary tract tumor liver neoplasm hepatobiliary system cancer endocrine gland cancer disease
 * human disease
 * DOID:3571
 * Liver cancer
 * Liver Cancer in Mouse Model (42507312762).jpg
 * liver carcinoma
 * class of disease
 * liver cancer carcinoma
 * liver cancer that has material basis in epithelial cells
 * DOID:686
 * liver carcinoma in situ
 * class of disease
 * in situ carcinoma liver disease
 * Human disease
 * DOID:9132
 * liver cirrhosis
 * class of disease
 * liver disease cirrosis disease
 * chronic disease of the liver, characterized by fibrosis
 * DOID:5082
 * C06.552.630 C23.550.355.412
 * Cirrhosis
 * Liver Cirrhosis.png
 * liver disease
 * class of disease
 * hepatobiliary disease endocrine system disease disease
 * disorder of the human liver
 * DOID:409
 * C06.552
 * Diseases and disorders of liver
 * liver fibroma
 * class of disease
 * liver neoplasm fibroma
 * Human disease
 * DOID:907
 * liver fibrosarcoma
 * class of disease
 * liver sarcoma fibrosarcoma
 * fibrosarcoma of soft tissue and sarcoma of liver that is located in the liver
 * DOID:8022
 * liver inflammatory pseudotumor
 * class of disease
 * Inflammatory pseudotumor inflammatory myofibroblastic tumour rare hepatic disease liver neoplasm rare hepatic and biliary tract tumor endocrine gland cancer liver disease
 * Human disease
 * DOID:918
 * liver leiomyoma
 * class of disease
 * liver neoplasm
 * Human disease
 * DOID:917
 * liver leiomyosarcoma
 * class of disease
 * liver sarcoma
 * leiomyosarcoma and sarcoma of liver that is located in the liver
 * DOID:5296
 * liver lipoma
 * class of disease
 * liver neoplasm gastrointestinal system benign neoplasm endocrine organ benign neoplasm
 * human disease
 * DOID:10190
 * liver lymphoma
 * class of disease
 * liver cancer endocrine gland cancer gastrointestinal lymphoma rare hepatic disease lymphoma
 * Human disease
 * DOID:901
 * liver neoplasm
 * class of disease
 * liver tumor hepatobiliary neoplasm liver disease endocrine organ benign neoplasm
 * human disease
 * DOID:916
 * C04.588.274.623 C06.301.623 C06.552.697
 * Benign neoplasms of liver
 * liver rhabdomyosarcoma
 * class of disease
 * liver sarcoma
 * rhabdomyosarcoma and sarcoma of liver that are located in the liver
 * DOID:4047
 * liver sarcoma
 * class of disease
 * liver cancer
 * sarcoma and malignant non-epithelial hepatic and intrahepatic bile duct neoplasm sthat is located in the liver
 * DOID:270
 * lobomycosis
 * class of disease
 * dermatomycosis disease
 * dermatomycosis that results in infection located in skin or located in subcutaneous tissue, has material basis in Lacazia loboi and has symptom crusty plaques, has symptom tumors and results in formation of nodular lesions
 * DOID:13026
 * C01.800.200.475 C01.150.703.302.475 C17.800.838.208.475
 * Lobomycosis
 * lobular neoplasia
 * class of disease
 * breast carcinoma in situ breast neoplasm
 * Human disease
 * DOID:3010
 * localized anterior staphyloma
 * class of disease
 * scleral staphyloma
 * Human disease
 * DOID:13787
 * localized chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5862
 * localized osteosarcoma
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3356
 * localized pulmonary fibrosis
 * class of disease
 * pulmonary fibrosis
 * Human disease
 * DOID:5642
 * localized scleroderma
 * class of disease
 * scleroderma
 * human disease
 * DOID:8472
 * C17.300.787 C17.800.767
 * Morphea
 * MercMorphea.JPG
 * locked-in syndrome
 * class of disease
 * neurological disorder disease
 * condition in which a patient is aware but cannot move or communicate verbally due to complete paralysis of nearly all voluntary muscles in the body except for vertical eye movements and blinking
 * DOID:12697
 * C10.597.622.760.500 C10.668.416 C23.888.592.636.786.500
 * CerebellumArteries.jpg
 * long QT syndrome 1
 * class of disease
 * long QT syndrome genetic disease autosomal dominant disease
 * A long QT syndrome that has material basis in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.
 * DOID:0110644
 * long QT syndrome 10
 * class of disease
 * long QT syndrome genetic disease autosomal dominant disease
 * A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.
 * DOID:0110651
 * long QT syndrome 4
 * class of disease
 * long QT syndrome autosomal dominant disease
 * human disease
 * DOID:0111701
 * long bone adamantinoma
 * class of disease
 * adamantinoma
 * adamantinoma that is located in the long bones and results in focal epithelial differentiation
 * DOID:2775
 * long bones of lower limb cancer
 * class of disease
 * bone cancer lower limb cancer
 * bone cancer that is manifested in the long bones of the lower limb
 * DOID:10149
 * loose anagen syndrome
 * class of disease
 * alopecia baldness
 * human disease
 * DOID:0111702
 * low compliance bladder
 * class of disease
 * bladder disease disease
 * human disease
 * DOID:12144
 * C12.777.829.866 C13.351.968.829.813 C23.888.942.343.780
 * low grade glioma
 * class of disease
 * glioma
 * A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma.
 * DOID:0080829
 * low implantation of placenta
 * class of disease
 * placenta praevia
 * Human disease
 * DOID:1677
 * low tension glaucoma
 * class of disease
 * open-angle glaucoma
 * Human disease
 * DOID:13544
 * C11.640.225
 * lower respiratory tract disease
 * class of disease
 * respiratory disease
 * respiratory system disease which involves the lower respiratory tract
 * DOID:0050161
 * lumbar plexus neoplasm
 * class of disease
 * nerve plexus neoplasm
 * Human disease
 * DOID:8389
 * lumbar spinal canal and spinal cord meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:7515
 * lumbosacral lipoma
 * class of disease
 * bone benign neoplasm lipoma
 * Human disease
 * DOID:7017
 * lumbosacral plexus lesion
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:13913
 * luminal breast carcinoma
 * class of disease
 * breast carcinoma breast carcinoma by gene expression profile
 * Human disease
 * DOID:0060548
 * luminal breast carcinoma B
 * class of disease
 * breast carcinoma luminal breast carcinoma
 * human disease
 * DOID:0080674
 * lung acinar adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * Human disease
 * DOID:6482
 * lung adenoid cystic carcinoma
 * class of disease
 * lung carcinoma adenoid cystic carcinoma
 * Human disease
 * DOID:4872
 * lung adenoma
 * class of disease
 * lung benign neoplasm benign epithelial neoplasm benign neoplasms by histologic type adenoma
 * Human disease
 * DOID:5386
 * lung benign neoplasm
 * class of disease
 * respiratory system benign neoplasm lung disease lung neoplasm thoracic cancer
 * human disease
 * DOID:3683
 * Benign neoplasms of bronchus and lung
 * lung carcinoma
 * class of disease
 * lung cancer carcinoma
 * lung cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the lungs and has symptom cough and has symptom chest discomfort or pain and has symptom weight loss and has symptom hemoptysis
 * DOID:3905
 * lung carcinoma in situ
 * class of disease
 * in situ carcinoma lung disease lung neoplasm
 * Human disease
 * DOID:8800
 * lung clear cell carcinoma
 * class of disease
 * clear cell carcinoma lung carcinoma
 * Human disease
 * DOID:7267
 * lung clear cell-sugar-tumor
 * class of disease
 * lung benign neoplasm perivascular epithelioid cell neoplasm benign perivascular tumor
 * Human disease
 * DOID:5763
 * lung combined large cell neuroendocrine carcinoma
 * class of disease
 * large cell neuroendocrine carcinoma of the lung combined carcinoma of lung
 * Human disease
 * DOID:7207
 * lung combined type small cell carcinoma
 * class of disease
 * lung small cell carcinoma combined carcinoma of lung
 * lung small cell carcinoma that is characterized as a multiphasic lung cancer comprised of a mixture of small cell and non-small cell lung carcinoma cells
 * DOID:5421
 * lung disease
 * class of disease
 * lower respiratory tract disease disease
 * respiratory disease
 * DOID:850
 * C08.381
 * lung hilum cancer
 * class of disease
 * lung cancer hilar lung neoplasm
 * Human disease
 * DOID:7696
 * lung leiomyoma
 * class of disease
 * lung benign neoplasm leiomyoma
 * Human disease
 * DOID:5136
 * lung leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * leiomyosarcoma and sarcoma of lung that is located in the lung
 * DOID:5265
 * lung lymphoma
 * class of disease
 * lung cancer lymphoma
 * Human disease
 * DOID:6760
 * lung meningioma
 * class of disease
 * lung cancer malignant neoplasm of meninges rare genetic respiratory disease genetic nervous system disorder ectopic meningioma
 * Human disease
 * DOID:5764
 * lung mixed small cell and squamous cell carcinoma
 * class of disease
 * pulmonary neuroendocrine tumor lung combined type small cell carcinoma
 * Human disease
 * DOID:7081
 * lung mucoepidermoid carcinoma
 * class of disease
 * lung carcinoma mucoepidermoid carcinoma
 * lung carcinoma that has material basis in a combination of squamous cells, mucus secreting cells and intermediate cells
 * DOID:0050932
 * Mucoepidermoid lung carcinoma
 * lung non-squamous non-small cell carcinoma
 * class of disease
 * non-small-cell lung carcinoma
 * lung non-small cell carcinoma that is characterized by the lack of evidence of squamous differentiation
 * DOID:0080521
 * lung oat cell carcinoma
 * class of disease
 * lung small cell carcinoma
 * Human disease
 * DOID:5411
 * lung occult adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * Human disease
 * DOID:7168
 * lung occult large cell carcinoma
 * class of disease
 * large-cell lung carcinoma lung occult non-small cell carcinoma
 * Human disease
 * DOID:7169
 * lung occult small cell carcinoma
 * class of disease
 * lung small cell carcinoma lung occult carcinoma
 * Human disease
 * DOID:5414
 * lung occult squamous cell carcinoma
 * class of disease
 * squamous cell carcinoma of the lung lung occult carcinoma
 * Human disease
 * DOID:6510
 * lung papillary adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * Human disease
 * DOID:5588
 * lung sarcoma
 * class of disease
 * lung cancer sarcoma
 * lung cancer that is located in the lung and that arises from transformed cells of mesenchymal origin
 * DOID:2784
 * Primary pulmonary sarcoma, NOS - Case 299 (15760799904).jpg
 * lung small cell carcinoma
 * class of disease
 * lung carcinoma small cell carcinoma
 * lung carcinoma that has material basis in primitive-appearing cells that are smaller than normal cells
 * DOID:5409
 * C04.588.894.797.520.109.220.624 C08.381.540.140.750 C08.785.520.100.220.750
 * [[File:Combined small cell lung carcinoma with extensive mucosal involvement; possible SCLC in situ Case 271 (9255562385).jpg|center|64px]]
 * lung superior sulcus carcinoma
 * class of disease
 * Pancoast tumor
 * human disease
 * DOID:8208
 * lupus erythematosus
 * class of disease
 * autoimmune disease autoimmune disease of musculoskeletal system disease
 * human disease
 * DOID:8857
 * Butterflyrash.jpg
 * lupus nephritis
 * class of disease
 * glomerulonephritis disease
 * inflammation of the kidneys
 * DOID:0080162
 * C12.200.777.419.570.363.680 C12.050.351.968.419.570.363.680 C17.300.480.680 C20.111.590.560 C12.950.419.570.363.680
 * Lupus nephritis
 * luteoma
 * class of disease
 * ovarian benign neoplasm ovarian disease disease
 * ovarian benign neoplasm characterized by solid proliferations of luteinized cells, resulting in a tumor-like ovarian enlargement that regresses during the puerperium
 * DOID:7880
 * C04.557.475.750.751 C04.588.322.455.464 C13.351.500.056.630.705.464 C13.351.937.418.685.464 C19.344.410.464 C19.391.630.705.464
 * Luteoma of pregnancy
 * luxation of globe
 * class of disease
 * globe disease
 * Human disease
 * DOID:1241
 * lymph node adenoid cystic carcinoma
 * class of disease
 * lymph node metastasis carcinoma lymph node cancer lymph node carcinoma
 * Human disease
 * DOID:0060219
 * lymph node cancer
 * class of disease
 * lymphatic system cancer lymph node neoplasm lymph node disease
 * lymphatic system cancer that is located in the lymph node
 * DOID:10619
 * Lymph node cancers
 * lymph node carcinoma
 * class of disease
 * carcinoma lymph node cancer
 * human disease
 * DOID:0080618
 * lymph node disease
 * class of disease
 * lymphatic system disease
 * Human disease
 * DOID:9942
 * Diseases and disorders of lymph nodes
 * lymph node palisaded myofibroblastoma
 * class of disease
 * lymph node cancer benign neoplasm of lymph node
 * human disease
 * DOID:8304
 * lymphadenitis
 * class of disease symptom or sign
 * lymph node disease clinical sign lymphatic system symptom adenitis
 * lymph node and lymph vessels inflammation
 * DOID:1602
 * C15.604.315
 * lymphangioma
 * class of disease
 * lymphatic system malformation benign blood vessel neoplasm disease
 * malformations of the lymphatic system characterized by lesions that are thin-walled cysts
 * DOID:1475
 * C04.557.375.450
 * Lymphangiomas
 * Lymphangioma.jpg
 * lymphangiosarcoma
 * class of disease
 * lymphatic system cancer angiosarcoma associated with lymphedema skin carcinoma skin sarcoma disease
 * lymphatic system cancer that has material basis in endothelial cells located in lymphatic vessels
 * DOID:2689
 * C04.557.375.480 C04.557.450.795.480
 * lymphatic system cancer
 * class of disease
 * immune system cancer lymphatic system disease
 * immune system cancer that is located in the lymphatic system and is characterized by uncontrolled cellular proliferation of lymphoid tissue
 * DOID:0060073
 * lymphatic system disease
 * class of disease
 * immune disorder
 * immune system disease that is located in the lymphatic system
 * DOID:75
 * C15.604
 * lymphoblastic leukemia
 * class of disease
 * leukemia
 * leukemia that has material basis in lymphoblasts (immature white blood cells)
 * DOID:1037
 * lymphoblastic lymphoma
 * class of disease symptom or sign
 * non-Hodgkin lymphoma lymphoma lymphatic system symptom
 * lymphoma that has material basis in immature malignant lymphocytes (lymphoblasts) committed to the B-cell or T-cell lineage and located in primarily lymph nodes or located in extranodal sites
 * DOID:0080147
 * lymphocele
 * class of disease
 * lymphatic system disease
 * Human disease
 * DOID:4347
 * C04.182.430 C15.604.510
 * lymphocytic gastritis
 * class of disease
 * gastritis chronic gastritis
 * Human disease
 * DOID:4035
 * lymphoepithelioma-like acinar prostate adenocarcinoma
 * class of disease
 * prostate adenocarcinoma prostatic acinar adenocarcinoma
 * Human disease
 * DOID:7246
 * lymphoepithelioma-like carcinoma
 * class of disease
 * carcinoma large cell carcinoma
 * carcinoma that is a malignant epithelial neoplasm densely infiltrated by lymphoid cells
 * DOID:5660
 * Lymphoepithelioma-like carcinoma
 * lymphoepithelioma-like thymic carcinoma
 * class of disease
 * thymic carcinoma
 * Human disease
 * DOID:7599
 * lymphohistiocytoid mesothelioma
 * class of disease
 * malignant pleural mesothelioma sarcomatoid mesothelioma
 * Human disease
 * DOID:7381
 * lymphoid interstitial pneumonia
 * class of disease
 * idiopathic interstitial pneumonia lymphoproliferative disorders
 * Human disease
 * DOID:0050159
 * lymphoma
 * class of disease symptom or sign
 * hematologic cancer lymphatic system cancer lymphoma and pseudolymphoma lymphoid neoplasm disease
 * hematologic cancer that affects lymphocytes
 * DOID:0060058
 * C04.557.386 C15.604.515.569 C20.683.515.761
 * Lymphomas
 * Gastric MALT lymphoma 2.jpg
 * lymphoma-like variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:7972
 * lymphopenia
 * class of disease symptom or sign
 * leukopenia lymphatic system symptom disease
 * leukopenia that is the condition of having an abnormally low level of lymphocytes in the blood
 * DOID:614
 * C15.378.553.546.605 C20.673.627 C15.378.243.750.605
 * lymphoplasmacyte-rich meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:4591
 * lysosomal and lipase deficiency
 * class of disease
 * lipid storage disease
 * lipid storage disease characterized by lysosomal and lipase deficiency
 * DOID:0080217
 * macrocystic neurilemmoma
 * class of disease
 * neurilemmoma
 * Human disease
 * DOID:3203
 * macrocystic pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:7097
 * macrocytic anemia
 * class of disease symptom or sign
 * anemia
 * Human disease
 * DOID:2361
 * C15.378.071.252
 * macroglobulinemia
 * class of disease
 * plasma protein metabolism disease
 * Human disease
 * DOID:9080
 * macrotrabecular hepatoblastoma
 * class of disease
 * hepatoblastoma
 * Human disease
 * DOID:5798
 * macular degeneration
 * class of disease
 * retinal degeneration maculopathy blindness
 * retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye
 * DOID:4448
 * C11.768.585.439
 * Macular degeneration
 * Intermediate age related macular degeneration.jpg
 * macular hole
 * class of disease
 * retinal disease retinal perforation maculopathy
 * small break in the macula, located in the center of the eye&#39;s light-sensitive tissue called the retina
 * DOID:7633
 * Macular hole
 * macular keratitis
 * class of disease
 * keratitis
 * human disease
 * DOID:11871
 * macular retinal edema
 * class of disease
 * retinal edema maculopathy disease
 * Human disease
 * DOID:4449
 * C11.768.585.439.245
 * Macular edema
 * main bronchus cancer
 * class of disease
 * lung cancer
 * Human disease
 * DOID:3924
 * major depressive disorder
 * class of disease
 * depressive disorder mental depression disease
 * all-encompassing low mood accompanied by low self-esteem, and by loss of interest or pleasure in normally enjoyable activities
 * DOID:1470
 * F03.600.300.375
 * Major depressive disorder
 * Vincent Van Gogh - Sorrow.JPG
 * male breast cancer
 * class of disease
 * breast cancer male breast neoplasm
 * Human disease
 * DOID:1614
 * male genital organ stricture
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:12333
 * male genital organ vascular disease
 * class of disease
 * male reproductive system disease vascular disease
 * Human disease
 * DOID:12335
 * male infertility
 * class of disease symptom or sign
 * male reproductive system disease infertility sexual impotence disease
 * inability to father a child
 * DOID:12336
 * C12.294.365.700
 * Male infertility
 * male reproductive organ benign neoplasm
 * class of disease
 * reproductive organ benign neoplasm male reproductive system neoplasm male reproductive system disease
 * human disease
 * DOID:0060087
 * male reproductive organ cancer
 * class of disease
 * reproductive organ cancer male reproductive system neoplasm male reproductive system disease
 * cancer that is manifested in the male genital system
 * DOID:3856
 * male reproductive system disease
 * class of disease
 * reproductive system disease male urogenital disease
 * reproductive system disease that affects male reproductive organs
 * DOID:48
 * C12.294
 * Diseases and disorders of the male reproductive system
 * male urethral cancer
 * class of disease
 * urethral cancer
 * Human disease
 * DOID:736
 * maleic anhydride allergic asthma
 * class of disease
 * allergic asthma maleic anhydride exposure
 * allergic asthma that has allergic trigger maleic anhydride
 * DOID:0040049
 * malignant acrospiroma
 * class of disease
 * acrospiroma sweat gland cancer
 * Human disease
 * DOID:5570
 * Malignant acrospiroma
 * malignant adenofibroma
 * class of disease
 * carcinosarcoma
 * Human disease
 * DOID:4422
 * malignant adult ependymoma
 * class of disease
 * ependymal tumor anaplastic ependymoma
 * Human disease
 * DOID:5890
 * malignant anus melanoma
 * class of disease
 * anal cancer mucosal melanoma melanoma
 * Human disease
 * DOID:14145
 * malignant biphasic mesothelioma
 * class of disease
 * mesothelioma
 * Human disease
 * DOID:4486
 * malignant breast melanoma
 * class of disease
 * breast cancer
 * Human disease
 * DOID:4364
 * malignant cardiac germ cell tumor
 * class of disease
 * heart cancer
 * Human disease
 * DOID:14535
 * malignant cardiac peripheral nerve sheath neoplasm
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:14534
 * malignant childhood germ cell neoplasm
 * class of disease
 * pediatric germ cell tumor germ cell cancer childhood cancer
 * Human disease
 * DOID:8149
 * malignant ciliary body melanoma
 * class of disease
 * ciliary body cancer
 * Human disease
 * DOID:6524
 * malignant conjunctival melanoma
 * class of disease
 * conjunctival cancer ocular melanoma
 * Human disease
 * DOID:1751
 * malignant cystadenoma
 * class of disease
 * adenocarcinoma cystadenoma
 * human disease
 * DOID:60004
 * malignant cystic nephroma
 * class of disease
 * kidney cancer nephroblastoma childhood multilocular cystic kidney neoplasm kidney cortex disease
 * Human disease
 * DOID:7571
 * malignant dermis tumor
 * class of disease
 * skin cancer
 * Human disease
 * DOID:5274
 * malignant epithelial mesothelioma
 * class of disease
 * mesothelioma
 * Human disease
 * DOID:4489
 * malignant epithelioid hemangioendothelioma
 * class of disease
 * malignant hemangioma epithelioid hemangioendothelioma
 * A malignant hemangioma characterized by the presence of epithelioid endothelial cells. The neoplastic cells are arranged in cords and nests, which are embedded in a myxoid to hyalinized stroma.
 * DOID:0080190
 * malignant essential hypertension
 * class of disease
 * essential hypertension
 * Human disease
 * DOID:10823
 * malignant eyelid melanoma
 * class of disease
 * skin melanoma
 * Human disease
 * DOID:10040
 * malignant fibrous histiocytoma
 * class of disease
 * histiocytoma fibrous histiocytoma sarcoma
 * human disease
 * DOID:1907
 * malignant fibrous histiocytoma of bone
 * class of disease
 * connective tissue neoplasm osteosarcoma
 * Human disease
 * DOID:3352
 * malignant gastric germ cell tumor
 * class of disease
 * stomach cancer extragonadal germ cell cancer gastrointestinal system disease gastrointestinal system cancer
 * Human disease
 * DOID:6949 DOID:4716
 * malignant gastric granular cell tumor
 * class of disease
 * stomach cancer
 * Human disease
 * DOID:10536
 * malignant gastric teratoma
 * class of disease
 * malignant gastric germ cell tumor gastric teratoma extragonadal non-dysgerminomatous germ cell tumor
 * Human disease
 * DOID:6948
 * malignant giant cell tumor
 * class of disease
 * giant cell tumor connective tissue neoplasm
 * Human disease
 * DOID:2705
 * malignant giant cell tumor of soft parts
 * class of disease
 * malignant fibrous histiocytoma malignant giant cell tumor
 * Human disease
 * DOID:5638
 * malignant giant cell tumor of the tendon sheath
 * class of disease
 * synovium cancer
 * Human disease
 * DOID:2704
 * malignant glandular tumor of peripheral nerve sheath
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:8420
 * malignant granular cell esophageal tumor
 * class of disease
 * esophageal cancer granular cell tumor
 * Human disease
 * DOID:5040
 * malignant granular cell myoblastoma
 * class of disease
 * skin cancer malignant peripheral nerve neoplasm granular cell tumor
 * Human disease
 * DOID:5042
 * malignant granular cell skin tumor
 * class of disease
 * malignant dermis tumor malignant granular cell myoblastoma
 * Human disease
 * DOID:7639
 * malignant hemangioma
 * class of disease
 * sarcoma vascular cancer malignant mixed tumor
 * cell type cancer of vascular origin, characterized by proliferation of endothelial cells in and about the vascular lumen
 * DOID:0080189
 * malignant hypertension
 * class of disease symptom or sign
 * arterial hypertension hypertensive crisis disease
 * condition of markedly elevated blood pressure with diastolic pressure typically greater than 120 mm Hg
 * DOID:10824
 * C14.907.489.330
 * malignant hypertensive renal disease
 * class of disease
 * renal hypertension
 * Human disease
 * DOID:10177
 * malignant leptomeningeal tumor
 * class of disease
 * meningioma malignant neoplasm of meninges meningeal carcinomatosis
 * Human disease
 * DOID:6086
 * malignant mediastinal neurogenic neoplasm
 * class of disease
 * mediastinal cancer
 * mediastinal cancer that has material basis in neural cells
 * DOID:4691
 * malignant mediastinum hemangiopericytoma
 * class of disease
 * hemangiopericytoma hemangiopericytoma, malignant mediastinal cancer
 * hemangiopericytoma and sarcoma of the mediastinum that is located in the mediastinum
 * DOID:6209
 * malignant melanocytic neoplasm of the peripheral nerve sheath
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:6345
 * malignant melanocytic peripheral nerve sheath tumor of mediastinum
 * class of disease
 * mediastinal cancer peripheral neuropathy malignant melanocytic neoplasm of the peripheral nerve sheath mediastinum sarcoma nervous system cancer
 * Human disease
 * DOID:7077
 * malignant mesenchymoma
 * class of disease
 * mesenchymoma
 * Human disease
 * DOID:5758
 * malignant mixed tumor
 * class of disease
 * Mixed tumor cell type cancer
 * cell type cancer that has material basis in cells from two tissues
 * DOID:154
 * C04.557.435.525
 * malignant neoplasm of acoustic nerve
 * class of disease
 * cranial nerve malignant neoplasm vestibulocochlear nerve neoplasm inner ear cancer vestibulocochlear nerve disease ear neoplasms
 * Human disease
 * DOID:2814
 * malignant neoplasm of short bones of lower limb
 * class of disease
 * long bones of lower limb cancer
 * Human disease
 * DOID:10151
 * malignant oculomotor nerve tumor
 * class of disease
 * cranial nerve III tumor cranial nerve malignant neoplasm
 * Human disease
 * DOID:2816
 * malignant otitis externa
 * class of disease
 * otitis externa complications of diabetes mellitus
 * Human disease
 * DOID:10516
 * malignant ovarian Brenner tumor
 * class of disease
 * ovarian cancer ovarian Brenner tumor malignant ovarian surface epithelial-stromal neoplasm
 * malignant ovarian surface epithelial-stromal neoplasm that has material basis in the surface epithelium of the ovary
 * DOID:4217
 * malignant ovarian cyst
 * class of disease
 * ovarian cancer ovarian cyst
 * Human disease
 * DOID:2145
 * malignant ovarian germ cell neoplasm
 * class of disease
 * ovarian germ cell neoplasm rare gynecological tumor germ cell cancer ovarian cancer
 * Human disease
 * DOID:2155
 * malignant ovarian surface epithelial-stromal neoplasm
 * class of disease
 * surface epithelial-stromal tumor ovarian cancer
 * Human disease
 * DOID:2151
 * malignant parietal pleura tumor
 * class of disease
 * pleural cancer
 * Human disease
 * DOID:14032
 * malignant pediatric adrenal gland pheochromocytoma
 * class of disease
 * adrenal gland pheochromocytoma
 * adrenal gland pheochromocytoma that is characterized by rare chromaffin cell tumors which secrete catecholamines, and has a higher prevalence of hereditary factors and metastatis in children than adults
 * DOID:0070325
 * malignant peripheral nerve sheath tumor
 * class of disease
 * nerve sheath neoplasms malignant peripheral nerve neoplasm
 * Human disease
 * DOID:5940
 * Malignant peripheral nerve sheath tumor
 * malignant peritoneal solitary fibrous tumor
 * class of disease
 * peritoneum cancer peritoneal solitary fibrous tumor
 * Human disease
 * DOID:4490
 * malignant pheochromocytoma
 * class of disease
 * adrenal medulla cancer
 * adrenal medulla cancer that arises within the adrenal medulla, releasing epinephrines and norepinephrines hormones
 * DOID:0080347
 * malignant pineal area germ cell neoplasm
 * class of disease
 * pinealoma
 * Human disease
 * DOID:1660
 * malignant pleural mesothelioma
 * class of disease
 * pleural cancer benign pleural mesothelioma mesothelioma squamous cell carcinoma respiratory system cancer pleural disease
 * pleural cancer that has material basis in mesothelium cells
 * DOID:7474
 * Pleural mesothelioma
 * malignant renovascular hypertension
 * class of disease
 * malignant secondary hypertension renovascular hypertension renal hypertension
 * Human disease
 * DOID:13730
 * malignant secondary hypertension
 * class of disease
 * secondary hypertension
 * Human disease
 * DOID:13731
 * malignant skin fibrous histiocytoma
 * class of disease
 * malignant dermis tumor malignant fibrous histiocytoma
 * Human disease
 * DOID:1906
 * malignant spindle cell melanoma
 * class of disease
 * melanoma hemangiopericytoma spindle cell cancer
 * melanoma that is most commonly located in sun-exposed skin and results in formation of spindle-like shaped cells that have a high recurrence rate even with treatment
 * DOID:3162
 * malignant spiradenoma
 * class of disease
 * eccrine sweat gland cancer apocrine sweat gland cancer spiradenoma
 * Human disease
 * DOID:7960
 * malignant struma ovarii
 * class of disease
 * struma ovarii immature teratoma of ovary
 * Human disease
 * DOID:5208
 * malignant syringoma
 * class of disease
 * eccrine sweat gland cancer
 * Human disease
 * DOID:5569
 * malignant triton tumor
 * class of disease
 * malignant peripheral nerve sheath tumor
 * human disease
 * DOID:6707
 * malignant tumor of undescended testis
 * class of disease
 * testicular cancer cryptorchidism
 * Human disease
 * DOID:12276
 * malignant type A thymoma
 * class of disease
 * spindle cell thymoma
 * Human disease
 * DOID:7927
 * malignant type AB thymoma
 * class of disease
 * mixed type thymoma
 * Human disease
 * DOID:6723
 * malignant visceral pleura tumor
 * class of disease
 * pleural cancer
 * Human disease
 * DOID:14033
 * malt worker's lung
 * class of disease
 * extrinsic allergic alveolitis
 * extrinsic allergic alveolitis which is caused by inhalation of fungal spores of Aspergillus clavatus and Aspergillus fumigatus from moldy barley
 * DOID:2314
 * mammary Paget's disease
 * class of disease
 * breast adenocarcinoma disease
 * type of cancer that may have the appearance of eczema, involving the nipple
 * DOID:3443
 * C04.557.470.200.240.187.500 C04.557.470.615.275.625
 * Paget's disease of the breast
 * mammary analogue secretory carcinoma
 * class of disease
 * salivary gland cancer carcinoma salivary gland carcinoma secretory carcinoma
 * salivary gland neoplasm
 * DOID:0080808
 * C04.557.470.200.588
 * mammary myofibroblastoma
 * class of disease
 * benign neoplasm muscle tissue neoplasm breast benign neoplasm
 * rare, benign tumor of the breast
 * DOID:1629
 * mantle cell lymphoma
 * class of disease
 * B-cell lymphoma aggressive B-cell non-Hodgkin lymphoma disease
 * B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles
 * DOID:0050746
 * C04.557.386.480.525 C15.604.515.569.480.525 C20.683.515.761.480.525
 * Mantle cell lymphoma
 * Mantle cell lymphoma - intermed mag.jpg
 * marasmus
 * class of disease
 * protein-energy malnutrition disease
 * form of severe malnutrition characterized by energy deficiency
 * DOID:12328
 * Marasmus
 * Starved child.jpg
 * marginal corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10441
 * marginal zone B-cell lymphoma
 * class of disease
 * B-cell lymphoma leukocyte disease
 * group of lymphomas
 * DOID:0050748
 * Marginal zone lymphoma - kidney -- high mag.jpg
 * mast cell leukemia
 * class of disease
 * leukemia rare bone disease mastocytoma
 * rare leukemia (blood cancer) involving mast cells
 * DOID:9254
 * C04.557.337.440 C04.557.337.539.275.440 C20.762.750.750.500
 * Mast cell leukemia
 * mast cell sarcoma
 * class of disease
 * sarcoma mastocytoma
 * human disease
 * DOID:355
 * C04.557.450.565.465.124 C20.762.750.375
 * Mast Cell Sarcoma.jpg
 * mastitis
 * class of disease symptom or sign
 * breast disease breastfeeding difficulties inflammatory disease reproductive system disease skin and integumentary tissue symptom disease
 * inflammation of the breast
 * DOID:10690
 * C13.703.844.603 C17.800.090.968
 * Mastitis
 * [[File:Atlas of clinical surgery; with special reference to diagnosis and treatment for practitioners and students (1908) (14768289625).jpg|center|64px]]
 * mastocytoma
 * class of disease
 * tumor of hematopoietic and lymphoid tissues myeloid neoplasm
 * solid tumor consisting of mast cells, generally benign
 * DOID:3664
 * C04.557.450.565.465.249 C20.762.750.469
 * Mastocytoma
 * mastoiditis
 * class of disease
 * bone inflammation disease middle ear disease disease
 * middle ear disease characterized by an inflammation of the mucosal lining of the mastoid antrum and the mastoid air cell system inside the mastoid process
 * DOID:0060322
 * C01.539.160.495.500 C05.116.165.495.249 C09.218.705.663.652
 * Mastoiditis
 * Mastoiditis1.jpg
 * mature B-cell neoplasm
 * class of disease
 * B-cell lymphoma
 * Human disease
 * DOID:706
 * mature T-cell and NK-cell lymphoma
 * class of disease
 * non-Hodgkin lymphoma mature T-cell neoplasm
 * non-Hodgkin lymphoma that has material basis in mature T lymphocytes and natural killer cells
 * DOID:0050743
 * mature cataract
 * class of disease
 * senile cataract
 * Human disease
 * DOID:13717
 * mature gastric teratoma
 * class of disease
 * gastric teratoma mature teratoma
 * Human disease
 * DOID:8118
 * mature teratoma
 * class of disease
 * teratoma
 * Human disease
 * DOID:5566
 * Mature teratoma Case 164 (5462532633).jpg
 * mature teratoma of the ovary
 * class of disease
 * mature teratoma ovarian biphasic or triphasic teratoma ovarian germ cell teratoma
 * Human disease
 * DOID:6231
 * Mature teratoma of ovary
 * maturity-onset diabetes of the young
 * class of disease
 * diabetes autosomal dominant disease disease
 * genetic disease that has material basis in mutations in the MODY genes disrupting insulin production
 * DOID:0050524
 * maturity-onset diabetes of the young type 14
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young that has material basis in heterozygous mutation in the APPL1 gene on chromosome 3p14
 * DOID:0111111
 * maturity-onset diabetes of the young type 2
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young that has material basis in heterozygous mutation in the GCK gene on chromosome 7p13
 * DOID:0111100
 * maturity-onset diabetes of the young type 3
 * class of disease
 * maturity-onset diabetes of the young
 * A maturity-onset diabetes of the young that has material basis in mutation in the HNF1A gene on chromosome 12q24.31.
 * DOID:0111102
 * maturity-onset diabetes of the young type 4
 * class of disease
 * maturity-onset diabetes of the young
 * A maturity-onset diabetes of the young that has material basis in mutation in the PDX1 gene on chromosome 13q12.2.
 * DOID:0111103
 * maturity-onset diabetes of the young type 5
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young characterized by abnormal renal development resuting in non-diabetic kidney disease and diabetes that has material basis in mutation in the HNF1B gene on chromosome 17q12
 * DOID:0111101
 * maturity-onset diabetes of the young type 6
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young that has material basis in heterozygous mutation in the NEUROD1 gene on chromosome 2q31
 * DOID:0111104
 * maxillary sinus cancer
 * class of disease
 * paranasal sinus cancer maxillary sinus neoplasm
 * Human disease
 * DOID:1357
 * maxillary sinus cholesteatoma
 * class of disease
 * paranasal sinus disease cholesteatoma mouth disease
 * cholesteatoma located in paranasal sinus
 * DOID:867
 * maxillary sinusitis
 * class of disease
 * nose disease sinusitis mouth disease
 * sinusitis which involves infection of maxillary sinuses that causes pain or pressure over the cheeks just below the eyes, tooth ache, and headache
 * DOID:2051
 * C08.460.692.752.578 C08.730.749.578 C09.603.692.752.578 C01.748.749.578
 * mechanical ectropion
 * class of disease
 * ectropion
 * Human disease
 * DOID:1569
 * mechanical entropion
 * class of disease
 * entropion
 * Human disease
 * DOID:13112
 * mechanical lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:13037
 * mechanical strabismus
 * class of disease
 * strabismus
 * Human disease
 * DOID:9306
 * meconium aspiration syndrome
 * class of disease
 * lung disease perinatal respiratory disorder disease
 * Human disease
 * DOID:11049
 * C08.381.520.687 C08.618.580 C13.703.277.785 C16.300.580 C16.614.580
 * Meconium aspiration syndrome
 * Amniotic fluid and meconium aspiration Case 179 (5613700230).jpg
 * medial epicondylitis
 * class of disease
 * bone inflammation disease arm injuries disease
 * bone inflammation disease that results in inflammation located in epicondyle
 * DOID:14087
 * Golfer's elbow
 * Golfers-Elbow SAG.jpg
 * median arcuate ligament syndrome
 * class of disease
 * vascular surgery rare abdominal surgical disease syndrome
 * Human disease
 * DOID:9892
 * C06.198.929C14.240.850.922 C14.907.137.527 C16.131.240.850.898
 * Median arcuate ligament syndrome
 * median nerve neuropathy
 * class of disease
 * mononeuritis of upper limb and mononeuritis multiplex brachial plexus neuritis
 * Human disease
 * DOID:571
 * C10.668.829.500.500
 * mediastinal cancer
 * class of disease
 * thoracic cancer mediastinal neoplasm
 * thoracic cancer that is located in the mediastinum
 * DOID:5559
 * Mediastinal cancers
 * mediastinal granular cell myoblastoma
 * class of disease
 * malignant mediastinal neurogenic neoplasm granular cell tumor mediastinal neurilemmoma
 * Human disease
 * DOID:5046
 * mediastinal gray zone lymphoma
 * class of disease
 * gray zone lymphoma mediastinal malignant lymphoma
 * Human disease
 * DOID:6867
 * mediastinal lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3926
 * MediastinalLipomatosisCT.png
 * mediastinal malignant lymphoma
 * class of disease
 * mediastinal cancer lymphoma
 * Human disease
 * DOID:6868
 * mediastinal melanocytic neurilemmoma
 * class of disease
 * melanotic neurilemmoma
 * Human disease
 * DOID:6484
 * mediastinal mesenchymal tumor
 * class of disease
 * mediastinal neoplasm mesenchymal cell neoplasm
 * Human disease
 * DOID:5560
 * mediastinal neurilemmoma
 * class of disease
 * peripheral nerve schwannoma mediastinal neoplasm
 * Human disease
 * DOID:6175
 * mediastinal osteogenic sarcoma
 * class of disease
 * extraosseous osteosarcoma mediastinum sarcoma
 * Human disease
 * DOID:6208
 * mediastinitis
 * class of disease
 * connective tissue disease mediastinal disease inflammatory disease disease
 * inflammatory process affecting the mediastinum
 * DOID:819
 * C08.846.187.790
 * mediastinum angiosarcoma
 * class of disease
 * angiosarcoma mediastinum sarcoma
 * angiosarcoma and sarcoma of the mediastinum that is located in the mediastinum
 * DOID:4525
 * mediastinum leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of mediastinum thoracic benign neoplasm mediastinal neurilemmoma
 * Human disease
 * DOID:5123
 * mediastinum leiomyosarcoma
 * class of disease
 * mediastinum sarcoma leiomyosarcoma
 * leiomyosarcoma and sarcoma of the mediastinum that derive from smooth muscle and are usually located in the esophagus or located in the main vessels
 * DOID:5292
 * mediastinum liposarcoma
 * class of disease
 * liposarcoma mediastinum sarcoma
 * liposarcoma and mediastinum sarcoma that is located in the mediastinum
 * DOID:5713
 * mediastinum neurofibroma
 * class of disease
 * malignant mediastinal neurogenic neoplasm neurofibroma
 * Human disease
 * DOID:12064
 * mediastinum rhabdomyosarcoma
 * class of disease
 * mediastinum sarcoma rhabdomyosarcoma
 * rhabdomyosarcoma and sarcoma of the mediastinum that is located in the mediastinum and affects children and adolescents
 * DOID:4049
 * mediastinum sarcoma
 * class of disease
 * mediastinal cancer sarcoma mediastinal soft tissue cancer
 * sarcoma and malignant mediastinal mesenchymnal tumor that is located in the mediastinum
 * DOID:4050
 * mediastinum seminoma
 * class of disease
 * mediastinal cancer extragonadal seminoma mediastinal malignant germ cell tumor germ cell cancer
 * Human disease
 * DOID:6249
 * mediastinum synovial sarcoma
 * class of disease
 * mediastinum sarcoma synovial sarcoma
 * sarcoma of the mediastinum and synovial sarcoma that is located in the mediastinum
 * DOID:5488
 * mediastinum teratoma
 * class of disease
 * mediastinal cancer mediastinal germ cell tumor teratoma
 * Human disease
 * DOID:5568
 * medullary colon carcinoma
 * class of disease
 * colon carcinoma
 * colon carcinoma that is characterized by a solid growth pattern
 * DOID:0080183
 * medulloadrenal hyperfunction
 * class of disease
 * adrenal gland disease
 * Human disease
 * DOID:12257
 * medulloblastoma SHH activated
 * class of disease
 * medulloblastoma
 * human disease
 * DOID:0080703
 * medulloblastoma SHH activated and TP53 mutant
 * class of disease
 * medulloblastoma SHH activated
 * human disease
 * DOID:0080704
 * medulloblastoma SHH activated and TP53 wild-type
 * class of disease
 * medulloblastoma SHH activated
 * human disease
 * DOID:0080705
 * medulloblastoma WNT activated
 * class of disease
 * medulloblastoma
 * human disease
 * DOID:0080702
 * medulloblastoma non-WNT/non-SHH
 * class of disease
 * medulloblastoma
 * human disease
 * DOID:0080706
 * medulloblastoma non-WNT/non-SHH group 3
 * class of disease
 * medulloblastoma non-WNT/non-SHH
 * human disease
 * DOID:0080707
 * medulloblastoma non-WNT/non-SHH group 4
 * class of disease
 * medulloblastoma non-WNT/non-SHH
 * human disease
 * DOID:0080708
 * medulloepithelioma
 * class of disease
 * central nervous system primitive neuroectodermal neoplasm
 * Human disease
 * DOID:4790
 * Medulloepithelioma
 * medullomyoblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3861
 * mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
 * class of disease
 * syndromic intellectual disability autosomal dominant disease
 * human disease
 * DOID:0111403
 * megacolon
 * class of disease
 * colonic disease disease
 * colonic disease that is characterized by an abnormal dilation of the colon
 * DOID:11372
 * C06.405.469.158.701
 * Megacolon
 * megaesophagus
 * class of disease
 * esophageal disease disease
 * abnormal dilation of the esophagus not due to obstruction
 * DOID:13186
 * megalencephalic leukoencephalopathy with subcortical cysts 1
 * class of disease
 * megalencephalic leukoencephalopathy with subcortical cysts genetic disease autosomal recessive disease
 * human disease
 * DOID:0080316
 * meibomian cyst
 * class of disease symptom or sign
 * internal hordeolum blepharitis disease
 * Cyst in the eyelid caused by chronic granulomatous inflammation of Meibomian gland
 * DOID:9903
 * C04.182.197 C11.338.300
 * Chalazion
 * Chalazion.JPG
 * melancholia
 * class of disease symptom or sign
 * major depressive disorder mental depression disease
 * DSM-IV subtype of clinical depression
 * DOID:2848
 * Accademia - La Meditazione by Domenico Fetti 1618.jpg
 * melanoacanthoma
 * class of disease
 * seborrheic keratosis
 * Human disease
 * DOID:11684
 * melanocytic psammomatous MPNST
 * class of disease
 * malignant melanocytic neoplasm of the peripheral nerve sheath
 * Human disease
 * DOID:6344
 * melanoma and neural system tumor syndrome
 * class of disease
 * hereditary neoplastic syndromes rare nervous system tumor rare genetic developmental defect during embryogenesis inherited nervous system cancer-predisposing syndrome nervous system cancer genetic nervous system disorder inherited tumor autosomal dominant disease syndrome
 * Melanoma and neural system tumor syndrome is an extremely rare tumor association characterized by dual predisposition to melanoma and neural system tumors (typically astrocytoma; see this term)
 * DOID:0111511
 * melanoma in congenital melanocytic nevus
 * class of disease
 * skin melanoma congenital melanocytic nevus
 * skin melanoma that arises from a congenital melanocytic nevus
 * DOID:0070327
 * melanoma with features of a Spitz nevus
 * class of disease
 * Spitzoid lesion melanoma skin melanoma
 * skin melanoma that is characterized by asymmetric shape, diameter greater than 1 cm, a lesion with a deep invasive component, and a high degree of cytologic atypia
 * DOID:0070326
 * Spitzoid melanoma
 * melanomatosis
 * class of disease
 * melanoma
 * Human disease
 * DOID:7206
 * melanotic medulloblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3868
 * melanotic neurilemmoma
 * class of disease
 * neurilemmoma
 * Human disease
 * DOID:3205
 * melanotic neuroectodermal tumor
 * class of disease
 * bone benign neoplasm neuroectodermal tumor
 * Human disease
 * DOID:166
 * C04.557.465.625.630 C04.557.580.625.630
 * Melanotic neuroectodermal tumor of infancy
 * Oral melanotic neuroectodermal tumor infancy LDRT 369 08.tif
 * melon allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Cucumis melo plant fruit food product.
 * DOID:0060509
 * melphalan allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger melphalan
 * DOID:0040066
 * membranous glomerulonephritis
 * class of disease
 * glomerulonephritis lupus nephritis disease
 * human disease
 * DOID:10976
 * C12.777.419.570.363.625 C13.351.968.419.570.363.625 C20.111.535
 * Membranous glomerulonephritis
 * meningeal melanocytoma
 * class of disease
 * central nervous system melanocytic neoplasm primary melanocytic tumor of central nervous system malignant neoplasm of meninges
 * Human disease
 * DOID:5900
 * meningeal melanoma
 * class of disease
 * malignant leptomeningeal tumor central nervous system melanocytic neoplasm
 * Human disease
 * DOID:6085
 * meningeal melanomatosis
 * class of disease
 * central nervous system melanocytic neoplasm melanomatosis malignant neoplasm of meninges
 * Human disease
 * DOID:8243
 * meninges hemangiopericytoma
 * class of disease
 * meningioma hemangiopericytoma malignant neoplasm of meninges
 * Human disease
 * DOID:4957
 * meninges sarcoma
 * class of disease
 * meningioma malignant neoplasm of meninges sarcoma
 * Human disease
 * DOID:7614
 * meningioma
 * class of disease
 * meningeal neoplasm central nervous system cancer disease
 * Tumor forms from meninges
 * DOID:3565
 * C04.557.580.520 C04.557.645.520 C04.588.614.250.580.500 C10.551.240.500.500
 * Meningioma
 * Contrast enhanced meningioma.jpg
 * meningitis
 * class of disease symptom or sign
 * encephalomyelitis central nervous system disease disease
 * inflammation of the membranes around the brain and spinal cord
 * DOID:9471
 * C10.228.614
 * Meningitis
 * Meninges-en.svg
 * meningocele
 * class of disease
 * spina bifida cephalocele
 * Human disease
 * DOID:1088
 * C10.500.680.598 C16.131.666.680.598 C23.300.707.968
 * meningococcal meningitis
 * class of disease
 * bacterial meningitis meningococcal disease
 * bacterial meningitis that has material basis in Neisseria meningitidis infection
 * DOID:0080176 DOID:9929
 * C01.150.252.223.500.750 C01.150.252.400.625.549.449 C10.228.228.180.500.750 C10.586.625.280.505 C01.207.180.500.750
 * meningoencephalitis
 * class of disease symptom or sign
 * central nervous system disease meningitis encephalitis neurological symptom disease
 * central nervous system disease that involves encephalitis which occurs along with meningitis
 * DOID:10554
 * C10.228.140.430.550 C10.228.228.245.550 C10.228.228.570 C01.207.245.550 C01.207.570 C10.586.250.550 C10.586.625.500
 * Méningo-encéphalite amibienne primitive.JPG
 * meningothelial meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:7212
 * meningovascular neurosyphilis
 * class of disease
 * tertiary neurosyphilis syphilitic meningitis
 * Human disease
 * DOID:0050491
 * mental depression
 * class of disease symptom or sign
 * mood disorder neurological and physiological symptom disease
 * state of low mood and aversion to activity, which can affect a person&#39;s thoughts, behavior, motivation, feelings, and sense of well-being
 * DOID:1596
 * F01.145.126.350
 * Depression (mood)
 * Depression-loss of loved one.jpg
 * mental disorder
 * class of disease
 * disease
 * distressing thought or behavior pattern
 * DOID:150
 * F03
 * Mental and behavioural diseases and disorders
 * Gautier - Salpetriere.JPG
 * mepivacaine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger mepivacaine
 * DOID:0040010
 * meropenem allergy
 * class of disease
 * beta-lactam allergy allergic asthma
 * beta-lactam allergy that has allergic trigger meropenem
 * DOID:0040038
 * mesangial proliferative glomerulonephritis
 * class of disease
 * glomerulonephritis proliferative glomerulonephritis lupus nephritis
 * glomerulonephritis associated primarily with the mesangium
 * DOID:4783
 * mesenchymal cell neoplasm
 * class of disease
 * cell type cancer
 * Human disease
 * DOID:3350
 * mesenchymal chondrosarcoma
 * class of disease
 * chondrosarcoma mesenchymal cell neoplasm small cell sarcoma
 * Human disease
 * DOID:4545
 * C04.557.450.565.280.280 C04.557.450.795.300.280
 * mesenchymoma
 * class of disease
 * connective tissue neoplasm
 * Human disease
 * DOID:2668
 * C04.557.435.500
 * mesenteric adenitis
 * class of disease
 * lymphadenitis adenitis
 * lymphadenitis
 * DOID:10782
 * C06.844.520 C15.604.315.618
 * Mesenteric adenitis
 * mesenteric vascular occlusion
 * class of disease
 * peripheral vascular disease mesenteric ischemia
 * Human disease
 * DOID:13252
 * C06.405.469.675 C06.844.550 C14.907.137.534
 * mesocestoidiasis
 * class of disease
 * parasitic helminthiasis infectious disease
 * parasitic helminthiasis infectious disease that involves parasitic cestode infection caused by Mesocestoides lineatus resulting in nausea, diarrhea, abdominal discomfort and vomiting
 * DOID:0050253
 * metabolic acidosis
 * class of disease
 * acidosis acquired metabolic disease disease
 * lactic acidosis that has material basis in high levels of acid
 * DOID:0050758
 * Metabolic acidosis
 * metabolic disease
 * class of disease
 * disease nutritional and metabolic diseases
 * disease that involving errors in metabolic processes of building or degradation of molecules
 * DOID:0014667
 * C18.452
 * Metabolic diseases and disorders
 * Ragged red fibres - gtc - very high mag.jpg
 * metachronous kidney Wilms' tumor
 * class of disease
 * nephroblastoma
 * Human disease
 * DOID:5178
 * metachronous osteosarcoma of the bone
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3379
 * metal allergy
 * class of disease
 * allergy
 * hypersensitivity reaction type I disease triggered by a metal
 * DOID:0060501
 * Metal allergies
 * metal metabolism disorder
 * class of disease
 * mineral metabolism disease inherited metabolic disorder
 * inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals
 * DOID:896
 * C16.320.565.618 C18.452.648.618
 * metanephric adenoma
 * class of disease
 * renal adenoma
 * Human disease
 * DOID:6404
 * Metanephric adenoma
 * metaphyseal dysplasia
 * class of disease
 * osteochondrodysplasia
 * osteochondrodysplasia that results in thinning and the tendency to fracture located in bone
 * DOID:0080019
 * metatypical basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4281
 * methemoglobinemia
 * class of disease
 * hemoglobinopathy disease
 * a form of toxic anemia characterized by the presence of methemoglobin in the blood
 * DOID:10783
 * C15.378.619
 * Methemoglobinemia
 * methotrexate-associated lymphoproliferation
 * class of disease
 * lymphoma
 * Human disease
 * DOID:5821
 * methyl isocyanate allergic asthma
 * class of disease
 * isocyanates allergic asthma
 * allergic asthma to isocyanates that has allergic trigger methyl isocyanate
 * DOID:0040044
 * methylmalonic acidemia cblB type
 * class of disease
 * methylmalonic acidemia genetic disease vitamin B12-responsive methylmalonic acidemia
 * Human disease
 * DOID:0060743
 * methylmalonic aciduria and homocystinuria type cblE
 * class of disease
 * methylmalonic acidemia methylmalonic acidemia with homocystinuria
 * Human disease
 * DOID:0050732
 * methylmalonic aciduria and homocystinuria type cblG
 * class of disease
 * methylmalonic acidemia methylmalonic acidemia with homocystinuria
 * Human disease
 * DOID:0050733
 * microcystic adenoma
 * class of disease
 * pancreatic cystadenoma benign neoplasms by histologic type
 * Human disease
 * DOID:5403
 * microcystic meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:4594
 * microcystic variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:7971
 * microglandular adenosis
 * class of disease
 * breast disease
 * Human disease
 * DOID:5998
 * microglandular adenosis of breast
 * class of disease
 * microglandular adenosis
 * Human disease
 * DOID:8335
 * microinvasive cervical squamous cell carcinoma
 * class of disease
 * cervical squamous cell carcinoma
 * Human disease
 * DOID:8409
 * microinvasive gastric cancer
 * class of disease
 * gastric adenocarcinoma
 * Human disease
 * DOID:10541
 * microlissencephaly
 * class of disease
 * lissencephaly
 * human disease
 * DOID:0112234
 * micronodular basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4289
 * microorchidism
 * class of disease
 * testicular disease hypogonadism, male
 * congenital human disease
 * DOID:11994
 * Microorchidism
 * Mikroorchie.jpg
 * micropapillary variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:6976
 * micropapillomatosis labialis
 * class of disease
 * vulvar squamous papilloma Vestibular papillomatosis
 * Human disease
 * DOID:6569
 * microphthalmia with brain and digit anomalies
 * class of disease
 * syndromic microphthalmia autosomal dominant disease
 * human disease
 * DOID:0111805
 * microphthalmia–dermal aplasia–sclerocornea syndrome
 * class of disease
 * syndromic microphthalmia syndrome
 * human disease
 * DOID:0111875
 * microscopic breast papilloma
 * class of disease
 * breast duct papilloma
 * Human disease
 * DOID:8225
 * microscopic colitis
 * class of disease
 * colitis disease
 * colitis that can only be diagnosed by the examination of colon tissue under a microscope
 * DOID:0060182
 * C06.405.205.265.173 C06.405.469.158.188.173
 * Microscopic colitis
 * middle cerebral artery infarction
 * class of disease
 * cerebral arterial disease cerebral infarction cerebral artery occlusion
 * human disease
 * DOID:3525
 * C10.228.140.300.150.477.200.450 C10.228.140.300.510.200.387 C10.228.140.300.775.200.200.450 C14.907.253.092.477.200.450 C14.907.253.560.200.387 C14.907.253.855.200.200.450
 * middle ear adenoma
 * class of disease
 * sensory organ benign neoplasm middle ear disease neoplasm of middle ear benign neoplasms by histologic type benign neoplasm of ear
 * Human disease
 * DOID:5387
 * middle ear cancer
 * class of disease
 * neoplasm of middle ear auricular cancer middle ear disease
 * auditory system cancer that is located in the middle ear
 * DOID:5099
 * middle ear cholesterol granuloma
 * class of disease
 * otitis media cholesteatoma
 * Human disease
 * DOID:10852
 * middle lobe syndrome
 * class of disease
 * lung disease atelectasis
 * human disease
 * DOID:2810
 * C08.381.730.542
 * midface dysplasia
 * class of disease
 * osteochondrodysplasia disease
 * Human disease
 * DOID:0050767
 * midline cystocele
 * class of disease
 * pelvic organ prolapse cystocele
 * Human disease
 * DOID:14131
 * migraine
 * class of disease
 * encephalopathy disease
 * disorder resulting in recurrent moderate-severe headaches
 * DOID:6364
 * C10.228.140.546.399.750
 * Migraine
 * Migraine.jpg
 * migraine with aura
 * class of disease
 * migraine
 * migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon
 * DOID:10024
 * C10.228.140.546.399.750.250
 * migraine without aura
 * class of disease
 * migraine rare genetic headache disorder
 * migraine that is characterized by migraine headaches that are not accompanied by an aura
 * DOID:12783
 * C10.228.140.546.399.750.450
 * mild pre-eclampsia
 * class of disease
 * pre-eclampsia
 * pre-eclampsia characterized by the presence of hypertension without evidence of end-organ damage, in a woman who was normotensive before 20 weeks&#39; gestation
 * DOID:10590
 * miliaria
 * class of disease
 * sweat gland disease disease
 * Human disease
 * DOID:1382
 * C17.800.946.492
 * Miliaria (disease)
 * miliaria profunda
 * class of disease
 * miliaria
 * miliaria that is characterized by ductal occlusion of the papillary dermis causing the gland&#39;s secretions to leak between the superficial and deep layers of the skin resulting in a rapidly-spreading flesh-colored rash
 * DOID:0070320
 * miliaria pustulosa
 * class of disease
 * miliaria
 * miliaria that is characterized by pustules resulting from inflammation and bacterial infection
 * DOID:0070319
 * miliaria rubra
 * class of disease
 * miliaria
 * Human disease
 * DOID:11153
 * Miliaria rubra
 * milk allergy
 * class of disease
 * food allergy disease
 * type of food allergy caused by milk
 * DOID:4376
 * C20.543.480.370.500
 * Milk allergy
 * Koemelkallegie-Eczeem in knieholte.jpg
 * mineral metabolism disease
 * class of disease
 * acquired metabolic disease disorder of metabolite absorption and transport
 * acquired metabolic disease that is characterized by abnormal mineral metabolism
 * DOID:0050032
 * Disorders of mineral metabolism
 * minor vestibular glands adenoma
 * class of disease
 * vestibular gland benign neoplasm adenoma
 * Human disease
 * DOID:2075
 * mirror agnosia
 * class of disease
 * agnosia visual agnosia
 * agnosia that is a loss of the ability to acknowledge objects in the neglected field that are visible when a mirror reflects the object visible in the non-neglected field
 * DOID:0060144
 * mirror movement disorder
 * class of disease
 * synkinesis movement disorders
 * movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs
 * DOID:0111153
 * mitochondrial DNA depletion syndrome 12b
 * class of disease
 * autosomal recessive disease mitochondrial DNA depletion syndrome mitochondrial DNA depletion syndrome 12
 * human disease
 * DOID:0080335
 * mitochondrial DNA depletion syndrome 14
 * class of disease
 * mitochondrial DNA depletion syndrome
 * human disease
 * DOID:0080336
 * mitochondrial DNA depletion syndrome 15
 * class of disease
 * autosomal recessive disease mitochondrial DNA depletion syndrome
 * human disease
 * DOID:0080337
 * mitochondrial DNA depletion syndrome 17
 * class of disease
 * mitochondrial DNA depletion syndrome
 * human disease
 * DOID:0070448
 * mitochondrial DNA depletion syndrome 8b
 * class of disease
 * mitochondrial DNA depletion syndrome autosomal recessive disease
 * human disease
 * DOID:0070331
 * mitochondrial complex III deficiency
 * class of disease
 * mitochondrial disease
 * mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III
 * DOID:0111139
 * mitochondrial complex V (ATP synthase) deficiency
 * class of disease
 * mitochondrial disease mitochondrial complex deficiency
 * mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex
 * DOID:0111143
 * mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1
 * class of disease
 * mitochondrial complex V (ATP synthase) deficiency
 * human disease
 * DOID:0111748
 * mitochondrial complex V (ATP synthase) deficiency nuclear type 6
 * class of disease
 * mitochondrial complex V (ATP synthase) deficiency
 * human disease
 * DOID:0111749
 * mitochondrial nonsyndromic sensorineural deafness
 * class of disease
 * sensorineural hearing loss mitochondrial deafness
 * human disease
 * DOID:0111751
 * mitochondrial type mitochondrial complex I deficiency
 * class of disease
 * mitochondrial complex I deficiency
 * human disease
 * DOID:0112100
 * mitochondrial type mitochondrial complex I deficiency 1
 * class of disease
 * mitochondrial type mitochondrial complex I deficiency
 * human disease
 * DOID:0112101
 * mitral valve disease
 * class of disease
 * heart valve disease
 * Human disease
 * DOID:61
 * Mitral valve diseases
 * mitral valve insufficiency
 * class of disease
 * mitral valve disease valve insufficiency disease
 * disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood
 * DOID:11502
 * C14.280.484.461
 * Mitral valve insufficiency
 * mitral valve stenosis
 * class of disease
 * mitral valve disease heart valve stenosis disease
 * mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart
 * DOID:1754
 * C14.280.484.517
 * Mitral valve stenosis
 * mixed astrocytoma-ependymoma
 * class of disease
 * mixed glioma
 * Human disease
 * DOID:7907
 * mixed astrocytoma-ependymoma-oligodendroglioma
 * class of disease
 * mixed glioma
 * Human disease
 * DOID:7817
 * mixed cell adenoma
 * class of disease
 * adenoma
 * Human disease
 * DOID:5385
 * mixed cell type adenoma of parathyroid
 * class of disease
 * parathyroid adenoma mixed cell adenoma
 * Human disease
 * DOID:7610
 * mixed cell type kidney Wilms' tumor
 * class of disease
 * nephroblastoma
 * Human disease
 * DOID:5179
 * mixed cerebral palsy
 * class of disease
 * cerebral palsy
 * subtype of cerebral palsy characterized by both the tight muscle tone of spastic cerebral palsy and the writhing, involuntary muscle movements of athetoid cerebral palsy
 * DOID:0050673
 * mixed ductal-endocrine carcinoma
 * class of disease
 * pancreatic ductal adenocarcinoma
 * Human disease
 * DOID:7716
 * mixed endometrial stromal and smooth muscle tumor
 * class of disease
 * uterine corpus cancer
 * Human disease
 * DOID:8302
 * mixed epithelial stromal tumour
 * class of disease
 * malignant mixed tumor
 * Human disease
 * DOID:5088
 * mixed epithelial tumor of ovary
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:6211
 * mixed epithelial/mesenchymal metaplastic breast carcinoma
 * class of disease
 * breast metaplastic carcinoma
 * Human disease
 * DOID:7541
 * mixed extragonadal germ cell cancer
 * class of disease
 * mixed germ cell cancer
 * mixed germ cell cancer that is located in areas of the body other than the ovary or testicle
 * DOID:0050907
 * mixed fibrolamellar hepatocellular carcinoma
 * class of disease
 * fibrolamellar hepatocellular carcinoma
 * fibrolamellar carcinoma that is characteirzed by the presence of both pure fibrolamellar hepatocellular carcinoma and conventional hepatocellular carcinoma components
 * DOID:0080182
 * mixed germ cell cancer
 * class of disease
 * germ cell cancer
 * germ cell cancer that occurs in many forms
 * DOID:3306
 * Mixed germ cell neoplasia
 * mixed germ cell-sex cord neoplasm
 * class of disease
 * malignant mixed tumor sex cord-gonadal stromal tumor
 * Human disease
 * DOID:2996
 * mixed glioma
 * class of disease
 * glioma
 * Human disease
 * DOID:5076
 * mixed gonadal dysgenesis X0/XY
 * class of disease
 * Turner syndrome gonadal dysgenesis disease
 * intersex variation
 * DOID:14449 DOID:0080656
 * C12.706.316.309.391 C12.706.316.795.249 C13.351.875.253.309.391 C13.351.875.253.795.249 C16.131.260.830.835.249 C16.131.939.316.309.391 C16.131.939.316.795.249 C16.320.180.830.835.249 C19.391.119.309.391 C19.391.119.795.249
 * mixed hepatoblastoma
 * class of disease
 * hepatoblastoma
 * Human disease
 * DOID:5789
 * mixed lacrimal gland cancer
 * class of disease
 * lacrimal gland cancer
 * Human disease
 * DOID:296
 * mixed liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5703
 * mixed malaria
 * class of disease
 * malaria
 * malaria that involves infection with more than one species of Plasmodium at the same time
 * DOID:14325
 * mixed oligodendroglioma-astrocytoma
 * class of disease
 * mixed glioma
 * Human disease
 * DOID:7912
 * mixed phenotype acute leukemia with MLL rearranged
 * class of disease
 * acute biphenotypic leukaemia
 * human disease
 * DOID:0081037
 * mixed phenotype acute leukemia, B/myeloid
 * class of disease
 * acute biphenotypic leukaemia
 * human disease
 * DOID:0081038
 * mixed receptive-expressive language disorder
 * class of disease
 * communication disorder
 * neurodevelopmental condition
 * DOID:12685
 * mixed sleep apnea
 * class of disease
 * sleep apnea
 * human disease
 * DOID:0080302
 * mixed testicular germ cell tumor
 * class of disease
 * testicular malignant germ cell cancer mixed germ cell cancer
 * mixed germ cell cancer that is located in the testis
 * DOID:4743
 * mixed type rhabdomyosarcoma
 * class of disease
 * rhabdomyosarcoma
 * Human disease
 * DOID:4065
 * mixed type thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:3280
 * mixed-type liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5709
 * mollusc allergy
 * class of disease
 * shellfish allergy
 * shellfish allergy triggered by Mollusca
 * DOID:0060523
 * molybdenum cofactor deficiency type A
 * class of disease
 * molybdenum cofactor deficiency genetic disease
 * human disease
 * DOID:0111164
 * monoclonal gammopathy of uncertain significance
 * class of disease
 * monoclonal gammopathy blood protein disease
 * human disease
 * DOID:7442
 * C15.378.147.542.640 C15.378.147.780.570 C20.683.460.640 C20.683.780.640
 * monoclonal paraproteinemia
 * class of disease
 * plasma protein metabolism disease paraproteinemia monoclonal gammopathy
 * Human disease
 * DOID:2346
 * monocular esotropia
 * class of disease
 * esotropia
 * Human disease
 * DOID:10293
 * monocular exotropia
 * class of disease
 * exotropia
 * Human disease
 * DOID:11853
 * monocyte, dendritic cell, and NK cell deficiency
 * class of disease
 * combined immunodeficiency
 * human disease
 * DOID:0111966
 * monocytic leukemia
 * class of disease
 * myeloid leukemia
 * type of myeloid leukemia characterized by a dominance of monocytes in the marrow
 * DOID:8527
 * monodermal teratoma
 * class of disease
 * ovarian germ cell teratoma
 * Human disease
 * DOID:5207
 * monofixation syndrome
 * class of disease
 * strabismus
 * Human disease
 * DOID:9843
 * Monofixation syndrome
 * monogenic disease
 * class of disease
 * genetic disease
 * Human disease
 * DOID:0050177
 * mononeuritis
 * class of disease
 * mononeuropathy
 * Human disease
 * DOID:1802
 * mononeuritis multiplex
 * class of disease
 * mononeuritis of upper limb and mononeuritis multiplex
 * Human disease
 * DOID:1835
 * mononeuritis of lower limb
 * class of disease
 * mononeuritis
 * Human disease
 * DOID:9473
 * mononeuritis of upper limb
 * class of disease
 * mononeuritis of upper limb and mononeuritis multiplex
 * Human disease
 * DOID:1844
 * mononeuritis of upper limb and mononeuritis multiplex
 * class of disease
 * mononeuritis
 * Human disease
 * DOID:572
 * mononeuropathy
 * class of disease
 * peripheral neuropathy disease
 * neuropathy that is characterized by damage to a single nerve, which results in loss of movement, sensation, or other function of that nerve
 * DOID:1188
 * C10.668.829.500
 * monophasic synovial sarcoma
 * class of disease
 * synovial sarcoma
 * Human disease
 * DOID:5495
 * mood disorder
 * class of disease
 * mental disorder
 * any of various disorders characterised primarily by disturbance in an individual&#39;s mood
 * DOID:3324
 * F03.600
 * Mood disorders
 * morbid obesity
 * class of disease
 * obesity
 * human disease
 * DOID:11981
 * C18.654.726.500.700 C23.888.144.699.500.500 E01.370.600.115.100.160.120.699.500.500 G07.100.100.160.120.699.500.500
 * Obesity
 * Morbid Obesity.jpg
 * morpheaform basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4292
 * morphine dependence
 * class of disease
 * opiate dependence
 * opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance
 * DOID:2560
 * C25.775.675.600
 * mosaic variegated aneuploidy syndrome
 * class of disease
 * syndrome aneuploidy
 * human disease
 * DOID:0080688
 * mosaic variegated aneuploidy syndrome 3
 * class of disease
 * autosomal recessive disease mosaic variegated aneuploidy syndrome
 * human disease
 * DOID:0080689
 * motility-related diarrhea
 * class of disease
 * diarrhea
 * Human disease
 * DOID:0050131
 * motor neuritis
 * class of disease
 * motor neuron disease
 * Human disease
 * DOID:683
 * motor neuron disease
 * class of disease
 * neurological disorder neurodegeneration disease
 * group of neurological disorders affecting motor neurons
 * DOID:231
 * C10.574.562 C10.668.467
 * Motor neuron diseases
 * mouth cancer
 * class of disease
 * gastrointestinal system cancer mouth disease oral cavity neoplasm head and neck cancer disease
 * gastrointestinal system cancer that is located in the oral cavity
 * DOID:8618
 * Oral cancer
 * ZungenCa2a.jpg
 * mouth disease
 * class of disease
 * gastrointestinal system disease stomatognathic disease disease of anatomical entity disease
 * gastrointestinal system disease that is located in the mouth
 * DOID:403
 * C07.465
 * Diseases and disorders of oral cavity, salivary glands and jaws
 * movement disorders
 * class of disease
 * encephalopathy motor dysfunction disease
 * clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements
 * DOID:480
 * C10.228.662
 * Movement disorders
 * mpox
 * class of disease symptom or sign notifiable disease
 * viral infectious disease Poxviridae infectious disease zoonosis disease
 * viral disease
 * DOID:3292
 * C01.925.256.743.615 C22.735.750 C22.795.600
 * Monkeypox
 * Monkeypox.jpg
 * mu chain disease
 * class of disease
 * heavy chain disease
 * heavy chain disease that results from an overproduction of mu antibody (IgM)
 * DOID:0060128
 * mucin-rich endometrial endometrioid adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:7293
 * mucinosis
 * class of disease
 * connective tissue disease metabolic disease
 * human disease
 * DOID:3141
 * C17.300.550
 * Mucinoses
 * mucinous adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, which produce mucin
 * DOID:3030
 * C04.557.470.200.025.075 C04.557.470.590.075
 * Pseudomyxoma peritonei
 * Invasive mucinous adenocarcinoma Case 250 (8207252350).jpg
 * mucinous adenofibroma
 * class of disease
 * adenofibroma
 * Human disease
 * DOID:2700
 * mucinous cystadenocarcinoma
 * class of disease
 * cystadenocarcinoma mucinous tumor
 * cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with a capsulated structure and mucus-producing cells
 * DOID:3603
 * C04.557.470.200.025.480.225 C04.557.470.590.480.225
 * [[File:Mucinous cystic tumor, atypical, uncertain malignant potential Case 252 (8211727496).jpg|center|64px]]
 * mucinous cystadenocarcinoma of the lung
 * class of disease
 * adenocarcinoma of the lung mucinous cystadenocarcinoma
 * lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue
 * DOID:0080304
 * mucinous cystadenofibroma
 * class of disease
 * cystadenofibroma
 * benign neoplasm characterized by the presence of cystic structures lined by mucinous columnar epithelial cells in a fibrotic stroma
 * DOID:6468
 * mucinous intrahepatic cholangiocarcinoma
 * class of disease
 * intrahepatic cholangiocarcinoma bile duct mucinous adenocarcinoma
 * Human disease
 * DOID:7024
 * mucinous lung adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung mucinous adenocarcinoma
 * lung adenocarcinoma with tumor cells floating in pools of mucin that distend alveolar spaces
 * DOID:0080303
 * mucinous ovarian cystadenoma
 * class of disease
 * ovarian cystadenoma mucinous cystadenoma
 * Human disease
 * DOID:3267
 * Mucinous cystoadenoma of the ovary
 * Mucinous Cystadenoma of Ovary (218889489).jpg
 * mucinous pancreas adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma mucinous adenocarcinoma
 * human disease
 * DOID:0080782
 * mucinous stomach adenocarcinoma
 * class of disease
 * gastric diffuse adenocarcinoma mucinous adenocarcinoma
 * Human disease
 * DOID:3716
 * mucinous tubular and spindle cell carcinoma
 * class of disease
 * renal cell carcinoma tubulopathy spindle cell carcinoma
 * human disease
 * DOID:4472
 * Mucinous tubular and spindle cell carcinoma
 * Renal Mucinous spindle 1.JPG
 * mucocele of appendix
 * class of disease
 * intestinal disease mucocele
 * Human disease
 * DOID:13248
 * mucoepidermoid esophageal carcinoma
 * class of disease
 * esophageal carcinoma mucoepidermoid carcinoma
 * Human disease
 * DOID:4686
 * mucoepidermoid thyroid carcinoma
 * class of disease
 * thyroid carcinoma mucoepidermoid carcinoma thyroid gland adenocarcinoma
 * Human disease
 * DOID:4687
 * mucolipidosis type III gamma
 * class of disease
 * pseudo-Hurler polydystrophy mucolipidosis autosomal recessive disease
 * human disease
 * DOID:0080678
 * mucopolysaccharidosis IV
 * class of disease
 * human disease
 * DOID:0050808
 * mucopolysaccharidosis Ih
 * class of disease
 * autosomal recessive disease mucopolysaccharidosis I
 * human disease
 * DOID:0111390
 * mucopolysaccharidosis Ih/s
 * class of disease
 * autosomal recessive disease mucopolysaccharidosis I
 * human disease
 * DOID:0111389
 * mucopolysaccharidosis type IIIA
 * class of disease
 * Sanfilippo syndrome autosomal recessive disease
 * human disease
 * DOID:0111395
 * mucopolysaccharidosis type IIIB
 * class of disease
 * Sanfilippo syndrome autosomal recessive disease
 * human disease
 * DOID:0111394
 * mucopolysaccharidosis type IIIC
 * class of disease
 * autosomal recessive disease Sanfilippo syndrome
 * human disease
 * DOID:0111393
 * mucopolysaccharidosis type IIID
 * class of disease
 * autosomal recessive disease Sanfilippo syndrome
 * human disease
 * DOID:0111402
 * mucopolysaccharidosis type IVA
 * class of disease
 * Morquio syndrome autosomal recessive disease
 * human disease
 * DOID:0111391
 * mucopolysaccharidosis type IVB
 * class of disease
 * autosomal recessive disease Morquio syndrome
 * human disease
 * DOID:0111392
 * mucormycosis
 * class of disease symptom or sign
 * zygomycosis opportunistic mycosis disease
 * fungal infection by the order Mucorales
 * DOID:8485 DOID:0050595
 * C01.150.703.980.600
 * [[File:Periorbital fungal infection known as mucormycosis, or phycomycosis PHIL 2831 lores.jpg|center|64px]]
 * mucosal melanoma
 * class of disease
 * melanoma extracutaneous melanoma
 * melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract
 * DOID:0050929
 * mucositis
 * class of disease
 * skin disease gastrointestinal system disease
 * gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract
 * DOID:0080178
 * C06.405.205.798 C07.465.584
 * Mucositis
 * multicentric papillary thyroid carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:7086
 * multicentric reticulohistiocytosis
 * class of disease
 * Reticulohistiocytosis syndrome
 * syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis
 * DOID:11824
 * multifocal dystonia
 * class of disease
 * dystonia
 * dystonia that involves two or more unrelated body parts
 * DOID:0050837
 * multifocal osteogenic sarcoma
 * class of disease
 * osteosarcoma bone sarcoma
 * Human disease
 * DOID:3360
 * multilocular cystic clear cell renal cell carcinoma
 * class of disease
 * renal cell carcinoma renal clear cell carcinoma
 * human disease
 * DOID:4463
 * multiminicore disease
 * class of disease
 * human disease
 * DOID:0080991
 * multinodular goiter
 * class of disease
 * goiter nodular goiter
 * goiter characterized by a multinodular enlargement of the thyroid gland
 * DOID:0050489
 * multiple benign circumferential skin creases on limbs
 * class of disease
 * skin disease
 * human disease
 * DOID:0112241
 * multiple chemical sensitivity
 * class of disease
 * syndrome
 * chronic medical condition of disputed but probably multifactorial etiology (genetic and non-genetic)
 * DOID:4661
 * C20.543.312.500 C21.223.500
 * Multiple chemical sensitivity
 * multiple congenital anomalies-hypotonia-seizures syndrome
 * class of disease
 * lipid metabolism disorder
 * lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency
 * DOID:0080503
 * multiple cranial nerve palsy
 * class of disease
 * glossopharyngeal nerve disease cranial nerve disease
 * Human disease
 * DOID:13866
 * multiple endocrine neoplasia
 * class of disease
 * endocrine gland neoplasm multiple polyglandular tumor
 * human disease
 * DOID:3125
 * C04.588.322.400 C04.651.600 C04.700.630 C16.320.700.630 C19.344.400
 * Multiple endocrine neoplasia
 * multiple epiphyseal dysplasia 2
 * class of disease
 * multiple epiphyseal dysplasia genetic disease autosomal dominant disease multiple epiphyseal dysplasia due to collagen 9 anomaly
 * multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A2 gene on chromosome 1p34
 * DOID:0070298
 * multiple epiphyseal dysplasia 3
 * class of disease
 * multiple epiphyseal dysplasia genetic disease multiple epiphyseal dysplasia due to collagen 9 anomaly autosomal dominant disease
 * multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A3 gene on chromosome 20q13
 * DOID:0070304
 * multiple epiphyseal dysplasia 7
 * class of disease
 * multiple epiphyseal dysplasia genetic disease autosomal recessive disease
 * multiple epiphyseal dysplasia that has material basis in homozygous mutation in the CANT1 gene on chromosome 17q25
 * DOID:0070302
 * multiple epiphyseal dysplasia due to collagen 9 anomaly
 * class of disease
 * multiple epiphyseal dysplasia genetic disease monogenic disease
 * multiple epiphyseal dysplasia that has material basis in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3)
 * DOID:0070305
 * multiple epiphyseal dysplasia with myopia and deafness
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0111348
 * multiple mitochondrial dysfunctions syndrome 6
 * class of disease
 * fatal multiple mitochondrial dysfunctions syndrome autosomal recessive disease
 * human disease
 * DOID:0070332
 * multiple mucosal neuroma
 * class of disease
 * neuroma
 * Human disease
 * DOID:5155
 * multiple myeloma
 * class of disease
 * leukocyte disease myeloid neoplasm immunoproliferative disorder disease
 * cancer of plasma cells
 * DOID:9538
 * C04.557.595.500 C14.907.454.460 C15.378.147.780.650 C15.378.463.515.460 C20.683.515.845 C20.683.780.650
 * Multiple myeloma
 * Plasmozytom multiple Osteolysen Unterarm.png
 * multiple spinal canal and spinal cord meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:7646
 * multisystem proteinopathy
 * class of disease
 * motor neuron disease
 * human disease
 * DOID:070355
 * mumps
 * class of disease symptom or sign
 * parotitis mumps virus infectious disease herpangina salivary gland disease disease
 * Human disease caused by paramyxovirus
 * DOID:10264
 * C01.925.782.580.600.680.500 C07.465.815.470.800.630
 * Mumps
 * Mumps.jpg
 * muscle neoplasm
 * class of disease
 * soft tissue neoplasm muscular disease
 * tumors or cancer located in muscle tissue or specific muscles
 * DOID:461
 * C04.588.839.500 C05.651.494
 * muscle tissue disease
 * class of disease
 * muscular disease
 * disease involving the muscle tissue
 * DOID:66
 * muscular atrophy
 * class of disease
 * muscular disease atrophic muscular disease clinical sign
 * human disease
 * DOID:767
 * C10.597.613.612 C23.300.070.500 C23.888.592.608.612
 * Muscle wasting
 * musculoskeletal disorder
 * class of disease
 * disease of anatomical entity
 * disease of anatomical entity that occurs in the muscular and/or skeletal system
 * DOID:17
 * C05
 * Diseases and disorders of the musculoskeletal system
 * Ankle Joint Arthritis.jpg
 * musculoskeletal system benign neoplasm
 * class of disease
 * organ system benign neoplasm musculoskeletal neoplasm
 * organ system benign neoplasm that is located in the muscular and skeletal organs
 * DOID:0060099
 * musculoskeletal system cancer
 * class of disease
 * organ system cancer musculoskeletal disorder musculoskeletal neoplasm
 * organ system cancer located in the muscular and skeletal organs and characterized by uncontrolled cellular proliferation of the musculoskeletal organs
 * DOID:0060100
 * mushroom workers' lung
 * class of disease
 * extrinsic allergic alveolitis
 * Human disease
 * DOID:2708
 * mycoplasma infection
 * class of disease
 * bacterial infectious disease primary Mycoplasmataceae infectious disease disease
 * bacterial infection with a species of the genus Mycoplasma
 * DOID:0050407 DOID:5461
 * C01.150.252.400.610.610
 * mycosis fungoides
 * class of disease
 * cutaneous T cell lymphoma rare disease mycosis fungoides and variants disease
 * Human disease
 * DOID:8691
 * C04.557.386.480.750.800.550 C15.604.515.569.480.750.800.550 C20.683.515.761.480.750.800.550
 * Mycosis fungoides
 * Mycosis fungoides knee.JPG
 * mycotic corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10440
 * myelitis
 * class of disease
 * spinal cord disease
 * spinal cord disease that is characterized by inflammation of the white matter or gray matter of the spinal cord
 * DOID:322
 * C10.228.228.618 C10.228.854.525
 * Myelitis
 * Living anatomy and pathology; (1910) (14571685858).jpg
 * myelodysplastic syndrome
 * class of disease
 * myeloproliferative disorders neoplastic syndrome disease
 * diverse collection of blood-related medical conditions with ineffective production of the myeloid class of blood cells
 * DOID:0050908
 * C15.378.190.625
 * Myelodysplastic syndrome
 * myelodysplastic/myeloproliferative neoplasm
 * class of disease
 * myeloid neoplasm
 * myeloid neoplasm that results in the overproduction of white blood cells
 * DOID:4972
 * myelofibrosis
 * class of disease
 * myeloid neoplasm acquired aplastic anemia rare genetic immune disease disease
 * myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue
 * DOID:4971
 * C15.378.190.636.765
 * Myelofibrosis, Reticulin Stain (6032644716).jpg
 * myeloid and lymphoid neoplasms associated with FGFR1 abnormalities
 * class of disease
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint
 * DOID:0080167
 * myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
 * class of disease
 * myeloid neoplasm associated with PDGFRA rearrangement myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRA gene, most often resulting in the formation of FIP1L1-PDGFRA fusion transcripts
 * DOID:0080165
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * class of disease
 * myeloid neoplasm myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1
 * human disease
 * DOID:0080164
 * myeloid leukemia
 * class of disease
 * leukemia disease
 * leukemia that is located in myeloid tissue
 * DOID:8692
 * C04.557.337.539
 * Myeloid leukemias
 * myeloid leukemia associated with Down Syndrome
 * class of disease
 * acute megakaryoblastic leukemia
 * human disease
 * DOID:0080798
 * myeloid neoplasm
 * class of disease
 * myeloproliferative disorders
 * a bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages.
 * DOID:0070004
 * myeloid neoplasms associated with PDGFRB rearrangement
 * class of disease
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRB gene, most often resulting in the formation of ETV6-PDGFRB fusion transcripts
 * DOID:0080166
 * myeloid sarcoma
 * class of disease
 * hematologic cancer
 * solid tumor composed of immature white blood cells[2] called myeloblasts.
 * DOID:8683
 * C04.557.337.539.775 C04.557.450.795.853
 * Myeloid sarcoma
 * myelophthisic anemia
 * class of disease
 * aplastic anemia
 * aplastic anemia that is characterized by displacement of hemopoietic bone-marrow tissue either by fibrosis, tumors or granulomas
 * DOID:2354
 * C15.378.071.307 C15.378.190.636.085
 * myeloproliferative disorder, chronic, with eosinophilia
 * class of disease
 * myeloproliferative disorders eosinophilia myeloproliferative neoplasm
 * human disease
 * DOID:0111344
 * myeloproliferative disorders
 * class of disease
 * bone marrow disease tumor of hematopoietic and lymphoid tissues connective tissue neoplasm hematologic cancer disease
 * hematopoietic disorders that derive from the blood-forming stem cells of the bone marrow
 * DOID:4960
 * C15.378.190.636
 * Myeloid neoplasms
 * myeloproliferative neoplasm
 * class of disease
 * myeloid neoplasm myeloproliferative disorders
 * myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood
 * DOID:2226
 * myoblastoma
 * class of disease
 * muscle neoplasm
 * human disease
 * DOID:5039
 * myocardial stunning
 * class of disease
 * myocardial infarction
 * state when some section of the myocardium (corresponding to area of a major coronary occlusion) shows a form of contractile abnormality
 * DOID:9767
 * C14.280.671 C23.888.582
 * myocarditis
 * class of disease symptom or sign
 * extrinsic cardiomyopathy myocardial disorder pancarditis cardiovascular system symptom disease
 * extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle
 * DOID:820
 * C14.280.238.625
 * Myocarditis
 * Viral myocarditis (1).JPG
 * myocardium cancer
 * class of disease
 * neoplasm of myocardium heart cancer
 * human disease
 * DOID:9299
 * myoclonic cerebellar dyssynergia
 * class of disease
 * neurodegeneration nervous system heredodegenerative disease Ramsay Hunt syndrome
 * degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment
 * DOID:12707
 * C10.228.140.252.700.250 C10.228.854.787.500 C10.574.500.825.250 C16.320.400.780.500
 * myoclonic dystonia 11
 * class of disease
 * myoclonic dystonia genetic disease autosomal dominant disease
 * myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has material basis in heterozygous mutation in the SGCE gene on chromosome 7q21
 * DOID:0090034
 * myoclonic dystonia 15
 * class of disease
 * myoclonic dystonia genetic disease autosomal dominant disease
 * myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11
 * DOID:0090035
 * myoepithelial carcinoma
 * class of disease
 * carcinoma
 * carcinoma that derives from myoepithelial cells
 * DOID:4838
 * myoepithelioma of the head and neck
 * class of disease
 * sweat gland neoplasm
 * neoplasm composed of outgrowths of myoepithelial cells from a sweat gland
 * DOID:2661
 * C04.557.435.585
 * Myoepithelioma of the head and neck
 * myofascial pain syndrome
 * class of disease
 * muscular disease medically unexplained physical symptom myalgia disease
 * human disease
 * DOID:431
 * C05.651.550
 * myofibrillar myopathy
 * class of disease
 * muscular disease
 * myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles
 * DOID:0080307
 * myofibrillar myopathy 10
 * class of disease
 * autosomal recessive disease myofibrillar myopathy
 * human disease
 * DOID:0112108
 * myofibrillar myopathy 3
 * class of disease
 * myofibrillar myopathy autosomal dominant disease
 * Human disease
 * DOID:0080094
 * myofibroma
 * class of disease
 * connective tissue neoplasm benign perivascular tumor connective tissue benign neoplasm
 * Human disease
 * DOID:4386
 * C04.557.450.565.540 C17.300.680.540
 * Lipoleiomyoma uterus.jpg
 * myoma
 * class of disease
 * muscle neoplasm uterine benign neoplasm disease
 * human disease
 * DOID:2691
 * C04.557.450.590.540
 * Uterine fibroids
 * Uterine fibroids.jpg
 * myopathy of extraocular muscle
 * class of disease
 * peripheral neuropathy rare eye disease muscular disease
 * myopathy that involves the extra-ocular muscle
 * DOID:929
 * myopathy, lactic acidosis, and sideroblastic anemia 1
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * human disease
 * DOID:0111185
 * myopathy, lactic acidosis, and sideroblastic anemia 2
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has material basis in homozyous or compound heterozygous mutation in YARS2 on 12p11.21.
 * DOID:0111186
 * myopathy, lactic acidosis, and sideroblastic anemia 3
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * human disease
 * DOID:0111184
 * myopathy, myofibrillar, 11
 * class of disease
 * myofibrillar myopathy
 * human disease
 * DOID:0081338
 * myopia
 * class of disease symptom or sign
 * refractive error visual impairment disease
 * visual defect which causes to see the near objects clearly and far objects unclearly
 * DOID:11830
 * C11.744.636
 * Myopia
 * Myopia.gif
 * myosarcoma
 * class of disease
 * musculoskeletal system cancer muscle tissue neoplasm muscular disease
 * musculoskeletal system cancer that is located in muscle
 * DOID:4045
 * C04.557.450.590.550 C04.557.450.795.550
 * myositis
 * class of disease
 * muscular disease inflammation disease
 * myopathy characterized by muscle inflammation
 * DOID:633
 * C05.651.594 C10.668.491.562
 * myositis fibrosa
 * class of disease
 * myositis
 * Human disease
 * DOID:9788
 * myositis ossificans
 * class of disease
 * myositis heterotopic ossification
 * myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles
 * DOID:668
 * C05.651.594.638
 * myotonic cataract
 * class of disease
 * cataract
 * Human disease
 * DOID:82
 * myotonic disease
 * class of disease
 * muscular dystrophy
 * muscular dystrophy characterized by progressive muscle wasting and weakness
 * DOID:450
 * C05.651.662 C10.668.491.606
 * myringitis bullosa hemorrhagica
 * class of disease
 * tympanic membrane disease disease
 * tympanic membrane disease that is characterized by blisters on the eardrum resulting from infection
 * DOID:13791
 * myxedema
 * class of disease
 * hypothyroidism mucinosis disease
 * Human disease
 * DOID:11634
 * C17.300.550.590 C19.874.482.638
 * Myxedema
 * myxofibrosarcoma
 * class of disease
 * fibrous histiocytoma skeletal muscle cancer rare nervous system tumor peripheral neuropathy fibrosarcoma fibromyxoid tumor sarcoma
 * A malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.
 * DOID:0080534
 * myxoid chondrosarcoma
 * class of disease
 * chondrosarcoma myxoid tumor
 * human disease
 * DOID:5861
 * myxoid leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5268
 * myxoid liposarcoma of the ovary
 * class of disease
 * liposarcoma of the ovary myxoid liposarcoma
 * Human disease
 * DOID:8023
 * myxomatous pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8081
 * myxopapillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5075
 * myxosarcoma
 * class of disease
 * sarcoma connective tissue neoplasm
 * human disease
 * DOID:4136
 * C04.557.450.565.560 C04.557.450.795.560
 * nail disease
 * class of disease
 * integumentary system disease
 * integumentary system disease that is located in nail
 * DOID:4123
 * C17.800.529
 * Diseases and disorders of the nails
 * nanophthalmos
 * class of disease
 * microphthalmia
 * human disease
 * DOID:0080634
 * narcissistic personality disorder
 * class of disease
 * personality disorder narcissism disease
 * personality disorder that involves an excessive preoccupation with issues of personal adequacy, power, prestige and vanity
 * DOID:2745
 * F03.675.500
 * Narcissistic personality disorder
 * Seesaw narcissism megalomania model.png
 * narcolepsy
 * class of disease
 * disease sleep disorder excessive daytime sleepiness
 * Human sleep disorder that involves an excessive urge to sleep and other neurological features
 * DOID:8986
 * C10.886.425.800.200.750 F03.870.400.800.200.750
 * Narcolepsy
 * nasal cavity cancer
 * class of disease
 * sensory system cancer nasal cancer nasal cavity neoplasm nasal cavity disease respiratory system cancer
 * respiratory system cancer that is located in the nasal cavity
 * DOID:10811
 * nasal cavity disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:2163
 * nasal cavity lymphoma
 * class of disease
 * nasal cavity cancer lymphoma
 * human disease
 * DOID:10813
 * nasal cavity olfactory neuroblastoma
 * class of disease
 * nasal cavity cancer esthesioneuroblastoma
 * Human disease
 * DOID:10812
 * nasopharyngeal disease
 * class of disease
 * upper respiratory tract disease pharyngeal diseases
 * respiratory disease
 * DOID:9561
 * C07.550.350 C09.775.350
 * nasopharyngitis
 * class of disease
 * nasopharyngeal disease
 * respiratory disease
 * DOID:10460
 * C07.550.350.700 C07.550.781.500 C08.730.561.500 C09.775.350.700 C09.775.649.500
 * natural killer cell leukemia
 * class of disease
 * lymphoblastic leukemia leukocyte disease rare bone disease immune disorder disease
 * Human disease
 * DOID:1035
 * near-fatal asthma
 * class of disease
 * acute asthma
 * human disease
 * DOID:0080823
 * necrobiosis lipoidica
 * class of disease
 * skin disease diabetic dermadrome necrobiotic disorders
 * human disease
 * DOID:3486
 * C17.300.200.495.545 C17.800.550.545 C17.800.849.495 C18.452.880.495
 * Necrobiosis lipoidica
 * Necrobiosislipoidica.jpg
 * necrosis of ear ossicle
 * class of disease
 * middle ear disease ear disease
 * Human disease
 * DOID:11783
 * necrosis of pituitary
 * class of disease
 * pituitary gland disease
 * endocrine disease
 * DOID:3646
 * necrotizing enterocolitis
 * class of disease
 * gastrointestinal system disease disease
 * human disease
 * DOID:8677
 * C06.405.205.596.700 C06.405.469.363.700
 * Neonatal necrotizing enterocolitis
 * necrotizing fasciitis
 * class of disease symptom or sign
 * fasciitis necrotizing soft tissue infection disease
 * infection that results in the death of the body&#39;s soft tissue
 * DOID:9602
 * C01.252.825.340 C05.321.550
 * Necrotizing fasciitis
 * Necrotizing fasciitis left leg.JPEG
 * necrotizing gastritis
 * class of disease
 * gastritis necrosis chronic gastritis
 * Human disease
 * DOID:4037
 * necrotizing sialometaplasia
 * class of disease
 * salivary gland disease disease
 * Human disease
 * DOID:12901
 * C07.465.815.802
 * Necrotizing sialometaplasia
 * nemaline myopathy 2
 * class of disease
 * nemaline myopathy genetic disease autosomal recessive disease
 * nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23
 * DOID:0110928
 * nemaline myopathy 3
 * class of disease
 * nemaline myopathy genetic disease autosomal recessive disease
 * nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42
 * DOID:0110927
 * neomycin sulfate allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis drug allergy
 * allergic contact dermatitis that has allergic trigger neomycin sulfate
 * DOID:0040067
 * neonatal anemia
 * class of disease
 * anemia
 * Human disease
 * DOID:11244
 * C15.378.071.363 C16.614.053
 * neonatal diabetes mellitus
 * class of disease
 * diabetes neonatal metabolic disturbances rare genetic diabetes mellitus
 * It is a congenital form of diabetes
 * DOID:11717
 * neonatal infective mastitis
 * class of disease
 * mastitis perinatal infectious disease
 * Human disease
 * DOID:13520
 * neonatal jaundice
 * class of disease
 * pigmentation disorder jaundice neonatal hyperbilirubinemia disease
 * pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant
 * DOID:2383
 * C16.614.451.500 C23.550.429.249.500
 * Neonatal jaundice
 * Jaundice phototherapy.jpg
 * neonatal leukemia
 * class of disease
 * childhood leukemia perinatal disease
 * Human disease
 * DOID:7756
 * neonatal myasthenia gravis
 * class of disease
 * myasthenia gravis
 * Human disease
 * DOID:14043
 * C10.114.656.650 C10.668.758.725.650 C20.111.258.500.650
 * neonatal period electroclinical syndrome
 * class of disease
 * electroclinical syndrome perinatal disease
 * electroclinical syndrome with onset in the neonatal period less than 44 weeks of gestational age
 * DOID:0050702
 * neonatal thyrotoxicosis
 * class of disease
 * thyrotoxicosis
 * endocrine disease
 * DOID:12573
 * neonatal urinary tract infectious disease
 * class of disease
 * urinary system disease urinary tract infection in children perinatal infectious disease
 * Human disease
 * DOID:1375
 * neonatal-onset type II citrullinemia
 * class of disease
 * citrullinemia autosomal recessive disease citrullinemia type II
 * human disease
 * DOID:0070341
 * neovascular glaucoma
 * class of disease
 * glaucoma glaucoma associated with vascular disorder rare acquired eye disease
 * Human disease
 * DOID:1687
 * C11.525.381.348
 * nephritis
 * class of disease symptom or sign
 * urological symptom disease
 * inflammation of the kidneys
 * DOID:10952
 * C12.777.419.570 C13.351.968.419.570
 * Nephritis
 * Diffuse proliferative lupus nephritis.jpg
 * nephrocalcinosis
 * class of disease
 * kidney disease calcinosis
 * Human disease
 * DOID:12679
 * C12.050.351.968.419.590 C12.200.777.419.590 C18.452.174.130.560 C12.950.419.590
 * Nephrocalcinosis
 * nephrogenic adenofibroma
 * class of disease
 * kidney benign neoplasm
 * Human disease
 * DOID:2698
 * nephrogenic adenoma of the urethra
 * class of disease
 * urethral benign neoplasm nephrogenic adenoma adenoma
 * Human disease
 * DOID:8109
 * nephrogenic adenoma of urinary bladder
 * class of disease
 * bladder benign neoplasm nephrogenic adenoma adenoma
 * Human disease
 * DOID:7333
 * nephrogenic diabetes insipidus type 2
 * class of disease
 * autosomal dominant disease nephrogenic diabetes insipidus autosomal recessive disease
 * human disease
 * DOID:0081061
 * nephrolithiasis
 * class of disease
 * kidney disease kidney stone disease
 * Human disease
 * DOID:585
 * C12.200.777.419.600 C12.200.777.967.249 C12.050.351.968.419.600 C12.050.351.968.967.249 C12.950.419.600 C12.950.967.249
 * nephroma
 * class of disease
 * kidney benign neoplasm kidney cortex disease
 * human disease
 * DOID:0080615
 * nephronophthisis
 * class of disease
 * autosomal recessive disease medullary cystic kidney disease kidney disease
 * congenital disorder of urinary system
 * DOID:12712
 * Nephronophthisis
 * nephronophthisis 1
 * class of disease
 * nephronophthisis
 * nephronophthisis that has material basis in homozygous or compound heterozygous mutation in or deletion of the NPHP1 gene on chromosome 2q13
 * DOID:0111112
 * nephropathia epidemica
 * class of disease
 * hemorrhagic fever with renal syndrome
 * human disease
 * DOID:0050201
 * nephrosclerosis
 * class of disease
 * renal hypertension disease
 * medical condition referring to damage to the kidney due to chronic high blood pressure
 * DOID:11664
 * C12.777.419.610 C13.351.968.419.610
 * nephrosis
 * class of disease
 * proteinuria kidney disease
 * non-inflammatory kidney disease
 * DOID:2527
 * C12.777.419.630 C13.351.968.419.630
 * Nephrosis
 * nephrotic syndrome 14
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080265
 * nephrotic syndrome 15
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080271
 * nephrotic syndrome 16
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080272
 * nephrotic syndrome type 1
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13
 * DOID:0080390
 * nephrotic syndrome type 17
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25
 * DOID:0080392
 * nephrotic syndrome type 18
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42
 * DOID:0080393
 * nephrotic syndrome type 19
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in compound heterozygous mutation in the NUP160 gene on chromosome 11p11
 * DOID:0080394
 * nephrotic syndrome type 2
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease nephrotic syndrome
 * human disease
 * DOID:0080379
 * nephrotic syndrome type 20
 * class of disease
 * familial nephrotic syndrome
 * human disease
 * DOID:0070357
 * nephrotic syndrome type 22
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0112268
 * nephrotic syndrome type 3
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has material basis in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23
 * DOID:0080382
 * nephrotic syndrome type 5
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p
 * DOID:0080380
 * nephrotic syndrome type 7
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080388
 * nephrotic syndrome type 8
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25
 * DOID:0080389
 * nephrotic syndrome, type 10
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080386
 * nephrotic syndrome, type 4
 * class of disease
 * nephrotic syndrome familial nephrotic syndrome autosomal dominant disease
 * human disease
 * DOID:0080383
 * nephrotic syndrome, type 6
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080384
 * nephrotic syndrome, type 9
 * class of disease
 * familial nephrotic syndrome
 * human disease
 * DOID:0080391
 * nerve compression syndrome
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:573
 * C10.668.829.550
 * Nerve compression syndromes
 * nerve fibre bundle defect
 * class of disease
 * visual pathway disease retinal disease
 * Human disease
 * DOID:5678
 * nerve plexus neoplasm
 * class of disease
 * peripheral nervous system neoplasm plexopathy
 * Human disease
 * DOID:4693
 * nerve root neoplasm
 * class of disease
 * peripheral nervous system neoplasm radiculopathy
 * Human disease
 * DOID:4698
 * nerve sheath neoplasms
 * class of disease
 * peripheral nervous system neoplasm neoplasm
 * peripheral nervous system neoplasm that is located in the connective tissue surrounding nerves
 * DOID:3193
 * C04.557.580.600 C10.551.775.500 C10.668.829.725.500
 * nervous system benign neoplasm
 * class of disease
 * organ system benign neoplasm neurological disorder nervous system neoplasm
 * organ system benign neoplasm that is located in the central nervous system or located in the peripheral nervous system
 * DOID:0060115
 * nervous system cancer
 * class of disease
 * organ system cancer nervous system neoplasm neurological disorder
 * organ system cancer located in the nervous system that affects the central or peripheral nervous system
 * DOID:3093
 * Nervous system neoplasms
 * nervous system hibernoma
 * class of disease
 * nervous system cancer hibernoma central nervous system lipoma
 * Human disease
 * DOID:6607
 * nervous system malformations
 * class of disease
 * congenital disorder central nervous system disease neurological disorder disease
 * congenital conditions that stem from damage to, or abnormal development of, the budding nervous system
 * DOID:2490
 * C10.500 C16.131.666
 * Congenital diseases and disorders of the nervous system
 * nested variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * human disease
 * DOID:7969
 * neurilemmoma
 * class of disease
 * neuroma disease
 * benign tumor of the nerve sheat composed of Schwann cells
 * DOID:3192
 * C04.557.465.625.650.595 C04.557.580.600.610.595 C04.557.580.625.650.595
 * Schwannoma
 * Peripheral schwannoma Antoni type A (1).JPG
 * neurilemmoma of the fifth cranial nerve
 * class of disease
 * trigeminal nerve neoplasm neurilemmoma
 * Human disease
 * DOID:3202
 * neurilemmoma of the pleura
 * class of disease
 * peripheral nerve schwannoma pleural disease respiratory system benign neoplasm rare respiratory disease benign neoplasm of pleura
 * Human disease
 * DOID:6564
 * neuritis
 * class of disease symptom or sign
 * peripheral neuropathy inflammation disease
 * inflammation of a nerve or the general inflammation of the peripheral nervous system
 * DOID:1803
 * C10.668.829.650
 * Neuritis
 * neuroaxonal dystrophy
 * class of disease
 * cerebral degeneration
 * Human disease
 * DOID:2367
 * C10.228.140.744
 * neurobehavioral disorder with prenatal alcohol exposure
 * class of disease
 * fetal alcohol spectrum disorders
 * human disease
 * DOID:0081052
 * neuroblastoma
 * class of disease cancer
 * autonomic nervous system neoplasm neuroblastic tumor disease childhood cancer
 * autonomic nervous system neoplasm derived from immature nerve cells
 * DOID:769
 * C04.557.465.625.600.590.650.550 C04.557.470.670.590.650.550 C04.557.580.625.600.590.650.550
 * Neuroblastoma
 * Neuroblastoma rosettes.jpg
 * neurocirculatory asthenia
 * class of disease
 * somatoform disorder
 * somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities.
 * DOID:11569
 * F03.080.500
 * neurodegeneration
 * class of disease
 * central nervous system disease degenerative disease disease
 * central nervous system disease
 * DOID:1289
 * C10.574
 * Neurodegenerative diseases and disorders
 * [[File:Parasagittal MRI of human head in patient with benign familial macrocephaly prior to brain injury (ANIMATED).gif|center|64px]]
 * neurodegeneration with brain iron accumulation
 * class of disease
 * iron metabolism disease neurodegeneration genetic neurodegenerative disease with dementia neuroaxonal dystrophy neurometabolic disease metabolic disease with dementia miscellaneous movement disorder due to genetic neurodegenerative disease
 * neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia
 * DOID:0110734
 * neurodegeneration with brain iron accumulation 2A
 * class of disease
 * neurodegeneration with brain iron accumulation genetic disease autosomal recessive disease
 * human disease
 * DOID:0110735
 * neurodegeneration with brain iron accumulation 2B
 * class of disease
 * neurodegeneration with brain iron accumulation Infantile neuroaxonal dystrophy genetic disease autosomal recessive disease
 * human disease
 * DOID:0110736
 * neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
 * class of disease
 * nervous system heredodegenerative disease neurodegeneration autosomal recessive disease
 * hereditary disease in humans
 * DOID:0070352
 * neurodermatitis
 * class of disease symptom or sign
 * dermatitis lichen disease
 * Human disease
 * DOID:3309
 * C17.800.174.660 C17.800.815.660
 * Lichen simplex chronicus
 * Lichen simplex chronicus 1.jpg
 * neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
 * class of disease
 * syndrome neurodevelopmental disorder
 * human disease
 * DOID:0070346
 * neurodevelopmental disorder with midbrain and hindbrain malformations
 * class of disease
 * syndromic intellectual disability genetic disease autosomal recessive disease
 * human disease
 * DOID:0080312
 * neuroectodermal tumor
 * class of disease
 * tumor nervous system cancer
 * Human disease
 * DOID:171
 * C04.557.465.625 C04.557.580.625
 * neuroendocrine carcinoma
 * class of disease
 * carcinoma neuroendocrine tumor
 * carcinoma that derives from neuroendocrine cells
 * DOID:1800
 * C04.557.465.625.650.240 C04.557.470.200.025.370 C04.557.580.625.650.240
 * Large cell neuroendocrine carcinoma Case 120 (4387600323).jpg
 * neuroendocrine tumor
 * class of disease
 * endocrine gland cancer rare disease disease
 * endocrine gland cancer that has material basis in neuroendocrine cells
 * DOID:169
 * C04.557.465.625.650 C04.557.580.625.650
 * Neuroendocrine tumors
 * neurofibroma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:962
 * C04.557.580.600.580 C10.551.775.500.750 C10.668.829.725.500.600
 * Neurofibroma
 * Neurofibroma (1).jpg
 * neurofibroma of gallbladder
 * class of disease
 * neurofibroma gallbladder cancer malignant peripheral nerve neoplasm liver cancer endocrine gland cancer
 * Human disease
 * DOID:5150
 * neurofibroma of spinal cord
 * class of disease
 * neurofibroma Spinal cord cancer
 * human disease
 * DOID:13742
 * neurofibroma of the esophagus
 * class of disease
 * gastrointestinal system disease gastrointestinal system cancer esophageal cancer neurofibroma
 * Human disease
 * DOID:961
 * neurofibroma of the heart
 * class of disease
 * malignant peripheral nerve neoplasm neurofibroma
 * Human disease
 * DOID:9300
 * neurofibromatosis type I
 * class of disease
 * neurofibromatoses neuro-cardio-facial-cutaneous syndromes disease
 * type of neurofibromatosis disease
 * DOID:0111253
 * C04.557.580.600.580.590.650 C04.700.645.650 C10.562.600.500 C10.574.500.549.400 C10.668.829.675 C16.320.400.560.400 C16.320.700.645.650
 * Neurofibromatosis type 1
 * Early neurofibromatosis.jpg
 * neurofibromatosis-Noonan syndrome
 * class of disease
 * syndrome autosomal dominant disease Noonan syndrome and Noonan-related syndrome neurofibromatosis type I
 * human disease
 * DOID:0111683
 * neurofibrosarcoma
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:3512
 * C04.557.450.565.590.350.590 C04.557.450.795.350.590 C04.557.580.600.580.795 C10.551.775.500.750.750 C10.668.829.725.500.600.600
 * neurogenic arthropathy
 * class of disease
 * arthropathy disease
 * Human disease
 * DOID:14286
 * C05.550.186
 * Neuropathic arthropathy
 * neurogenic bladder
 * class of disease
 * bladder disease urination disorder disease
 * Human disease
 * DOID:12143
 * C10.597.900 C12.200.777.829.839 C12.050.351.968.829.760 C23.888.592.900 C12.950.829.760C
 * Neurogenic bladder dysfunction
 * neurogenic bowel
 * class of disease
 * intestinal disease
 * Human disease
 * DOID:13419
 * C06.405.469.158.272.804
 * neurological disorder
 * class of disease
 * disease of anatomical entity disease
 * disease of an anatomical entity located in the central or peripheral nervous system
 * DOID:0060052 DOID:863
 * C10
 * Diseases and disorders of the nervous system
 * Pyramidal hippocampal neuron 40x.jpg
 * neuroma
 * class of disease
 * nervous system benign neoplasm peripheral nervous system neoplasm tumor
 * nervous system benign neoplasm that is characterized as a nerve tissue tumor
 * DOID:2001
 * C04.557.580.600.610
 * Neuroma
 * neuromuscular disease
 * class of disease
 * peripheral neuropathy musculoskeletal disorder disease
 * neuropathy that affect the nerves that control the voluntary muscles
 * DOID:440
 * C10.668
 * Neuromuscular diseases
 * neuromuscular junction disease
 * class of disease
 * neuromuscular disease
 * neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction
 * DOID:439
 * C10.668.758
 * neuronal ceroid lipofuscinosis
 * class of disease
 * lipid storage disease eye degenerative disease nervous system heredodegenerative disease
 * Human disease
 * DOID:14503
 * C10.574.500.550 C16.320.400.600 C16.320.565.398.641.509 C18.452.584.563.641.509 C18.452.648.398.641.509
 * neuronal ceroid lipofuscinosis 1
 * class of disease
 * neuronal ceroid lipofuscinosis Infantile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease juvenile neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110721
 * neuronal ceroid lipofuscinosis 10
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease adult neuronal ceroid lipofuscinosis congenital neuronal ceroid lipofuscinosis genetic disease
 * neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15
 * DOID:0110725
 * neuronal ceroid lipofuscinosis 2
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * A condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
 * DOID:0110726
 * neuronal ceroid lipofuscinosis 3
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis genetic disease
 * A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
 * DOID:0110731
 * neuronal ceroid lipofuscinosis 4A
 * class of disease
 * neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis genetic disease Kufs disease
 * human disease
 * DOID:0110730
 * neuronal ceroid lipofuscinosis 5
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * human disease
 * DOID:0110728
 * neuronal ceroid lipofuscinosis 6
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease adult neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110729
 * neuronal ceroid lipofuscinosis 7
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * human disease
 * DOID:0110722
 * neuronal ceroid lipofuscinosis 8
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease juvenile neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110723
 * neuronal ceroid lipofuscinosis 9
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis
 * neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seziures
 * DOID:0110733
 * neuronal intestinal dysplasia
 * class of disease
 * colonic disease intestinal pseudo-obstruction intestinal dysganglionosis
 * Human disease
 * DOID:0080072
 * neuronal intestinal dysplasia type A
 * class of disease
 * neuronal intestinal dysplasia
 * human disease
 * DOID:0080679
 * neuronal intestinal dysplasia type B
 * class of disease
 * neuronal intestinal dysplasia
 * human disease
 * DOID:0080680
 * neuronitis
 * class of disease
 * central nervous system disease neurological disorder inflammatory disease disease
 * central nervous system disease that is characterized by neuron inflammation
 * DOID:8117
 * neuronopathy, distal hereditary motor, type 5B
 * class of disease
 * nervous system heredodegenerative disease distal hereditary motor neuronopathy type 5
 * human disease
 * DOID:0111205
 * neurooculocardiogenitourinary syndrome
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0111675
 * neuropathy
 * class of disease
 * neurological disorder
 * disease of or damage to the nerves
 * DOID:870
 * Neuropathies
 * neuroretinitis
 * class of disease
 * optic papillitis focal chorioretinitis eye disease
 * Human disease
 * DOID:10176
 * neurosarcoidosis
 * class of disease
 * sarcoidosis central nervous system disease
 * disease with granulomas invoving nervous tissue
 * DOID:13403
 * Neurosarcoidosis
 * neurotrophic keratoconjunctivitis
 * class of disease
 * keratoconjunctivitis
 * Human disease
 * DOID:12125
 * neutropenia
 * class of disease
 * agranulocytosis disease
 * abnormally low concentration of neutrophils in the blood
 * DOID:1227
 * C15.378.553.546.184.564 C15.378.243.750.184.564
 * Neutropenia
 * Neutropenia.JPG
 * nevoid basal cell carcinoma syndrome
 * class of disease symptom or sign
 * autosomal dominant disease syndrome
 * an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma
 * DOID:2512
 * C04.182.089.530.690.150 C04.557.470.200.165.150 C04.557.470.565.165.150 C04.700.175 C05.116.099.105 C05.500.470.690.150 C07.320.450.670.130 C16.131.077.130 C16.320.700.175
 * nickel allergic asthma
 * class of disease
 * allergic asthma nickel sensitivity metal allergy
 * allergic asthma that has allergic trigger nickel atom
 * DOID:0040045
 * night blindness
 * class of disease
 * eye disease retinal disease vision disorder disease
 * condition making it difficult or impossible to see in relatively low light
 * DOID:8499
 * C11.966.671
 * Nyctalopia
 * P360 Onderdendam goed nachtzicht ns nachtblind.jpg
 * nipple carcinoma
 * class of disease
 * breast carcinoma malignant neoplasm of nipple
 * breast carcinoma that is located in the nipple
 * DOID:6629
 * nipple duct carcinoma
 * class of disease
 * nipple carcinoma
 * nipple carcinoma that is located in the nipple duct
 * DOID:7953
 * nipple neoplasm
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:3003
 * nocturnal asthma
 * class of disease
 * chronic asthma
 * human disease
 * DOID:0080826
 * nodal marginal zone B cell lymphoma
 * class of disease
 * marginal zone B-cell lymphoma
 * marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease
 * DOID:0080211
 * nodular basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4280
 * nodular degeneration of cornea
 * class of disease
 * corneal degeneration
 * Human disease
 * DOID:2879
 * nodular episcleritis
 * class of disease
 * scleral disease episcleritis
 * Human disease
 * DOID:728
 * nodular ganglioneuroblastoma
 * class of disease
 * ganglioneuroblastoma
 * Human disease
 * DOID:5193
 * nodular goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13197
 * C19.874.283.501
 * nodular hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:2061
 * nodular medulloblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3873
 * nodular melanoma
 * class of disease
 * skin melanoma
 * melanoma that is characterized as highly aggressive and manifests as a uniform blue-black, blue-red, or amelanotic nodule
 * DOID:10047
 * Nodular melanoma
 * nodular nonsuppurative panniculitis
 * class of disease
 * panniculitis subcutaneous tissue disease
 * cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin
 * DOID:1525
 * C17.300.710.500 C17.800.566.500
 * nodular prostate
 * class of disease
 * prostatic hypertrophy
 * Human disease
 * DOID:13206
 * nodular tenosynovitis
 * class of disease
 * connective tissue benign neoplasm
 * Human disease
 * DOID:2701
 * non specific chronic endometritis
 * class of disease
 * endometritis chronic endometritis
 * Human disease
 * DOID:4560
 * non-Hodgkin lymphoma
 * class of disease
 * lymphoma neoplasm hematopoietic system disease disease
 * type of cancer of lymph nodes
 * DOID:0060060
 * C04.557.386.480 C15.604.515.569.480 C20.683.515.761.480
 * Non-Hodgkin lymphomas
 * Mantle cell lymphoma - intermed mag.jpg
 * non-Langerhans-cell histiocytosis
 * class of disease
 * histiocytosis
 * Human disease
 * DOID:4330
 * C15.604.250.410
 * non-alcoholic fatty liver
 * class of disease
 * non-alcoholic fatty liver disease
 * nonalcoholic fatty liver disease that is characterized by the presence of at least 5% of hepatic steatosis with no evidence of hepatocellular injury in the form of hepatocyte ballooning
 * DOID:0080546
 * non-alcoholic fatty liver disease
 * class of disease
 * fatty liver disease disease
 * storing of excess fat in liver cells, not caused by heavy alcohol use
 * DOID:0080208
 * C06.552.241.519
 * non-alcoholic steatohepatitis
 * class of disease
 * non-alcoholic fatty liver disease
 * Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure.
 * DOID:0080547
 * non-arteritic anterior ischemic optic neuropathy
 * class of disease
 * anterior ischemic optic neuropathy
 * Human disease
 * DOID:0050864
 * non-congenital cyst of kidney
 * class of disease
 * cystic kidney disease
 * Human disease
 * DOID:9621
 * non-controlled substance abuse
 * class of disease
 * addiction substance use disorder social issue
 * abuse of chemical substances and/or abuse of any licit substances
 * DOID:9973
 * Substance dependence
 * Toxicoman - Substance abuse.jpg
 * non-functioning pancreatic endocrine tumor
 * class of disease
 * islet cell tumor non-functioning endocrine neoplasm
 * Human disease
 * DOID:7698
 * non-gestational choriocarcinoma
 * class of disease
 * choriocarcinoma
 * Human disease
 * DOID:4320
 * C04.557.465.955.207.438 C04.557.470.200.025.455.750 C04.850.908.208.438 C13.703.720.949.208.438
 * non-gestational ovarian choriocarcinoma
 * class of disease
 * ovarian primitive germ cell tumor choriocarcinoma of ovary
 * Human disease
 * DOID:7665
 * non-invasive bladder urothelial carcinoma
 * class of disease
 * bladder urothelial carcinoma
 * human disease
 * DOID:6571
 * non-proliferative fibrocystic change of the breast
 * class of disease
 * breast fibrocystic disease
 * Human disease
 * DOID:5997
 * non-renal secondary hyperparathyroidism
 * class of disease
 * hyperparathyroidism secondary hyperparathyroidism
 * Human disease
 * DOID:13575
 * non-secretory myeloma
 * class of disease
 * multiple myeloma non-functioning endocrine neoplasm
 * Human disease
 * DOID:9547
 * non-small-cell lung carcinoma
 * class of disease
 * lung carcinoma lung cancer disease
 * any type of epithelial lung cancer other than small-cell lung carcinoma
 * DOID:3908
 * C04.588.894.797.520.109.220.249 C08.381.540.140.500 C08.785.520.100.220.500
 * Non-small cell lung cancer
 * non-suppurative otitis media
 * class of disease
 * otitis media
 * otitis media which involves transudation of fluid in the middle ear without pus formation
 * DOID:11180
 * non-syndromic X-linked intellectual disability 1
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112038
 * non-syndromic X-linked intellectual disability 100
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112040
 * non-syndromic X-linked intellectual disability 101
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112048
 * non-syndromic X-linked intellectual disability 103
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112020
 * non-syndromic X-linked intellectual disability 104
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112018
 * non-syndromic X-linked intellectual disability 105
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112036
 * non-syndromic X-linked intellectual disability 107
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112054
 * non-syndromic X-linked intellectual disability 14
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112027
 * non-syndromic X-linked intellectual disability 19
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112019
 * non-syndromic X-linked intellectual disability 2
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112016
 * non-syndromic X-linked intellectual disability 20
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112023
 * non-syndromic X-linked intellectual disability 21
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112022
 * non-syndromic X-linked intellectual disability 23
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112049
 * non-syndromic X-linked intellectual disability 30
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112051
 * non-syndromic X-linked intellectual disability 41
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112058
 * non-syndromic X-linked intellectual disability 42
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112057
 * non-syndromic X-linked intellectual disability 45
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112028
 * non-syndromic X-linked intellectual disability 46
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112055
 * non-syndromic X-linked intellectual disability 50
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112029
 * non-syndromic X-linked intellectual disability 53
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112047
 * non-syndromic X-linked intellectual disability 58
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112024
 * non-syndromic X-linked intellectual disability 63
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112050
 * non-syndromic X-linked intellectual disability 72
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112059
 * non-syndromic X-linked intellectual disability 73
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112017
 * non-syndromic X-linked intellectual disability 77
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112039
 * non-syndromic X-linked intellectual disability 81
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112033
 * non-syndromic X-linked intellectual disability 82
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112052
 * non-syndromic X-linked intellectual disability 84
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112030
 * non-syndromic X-linked intellectual disability 88
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112053
 * non-syndromic X-linked intellectual disability 89
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112031
 * non-syndromic X-linked intellectual disability 9
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112034
 * non-syndromic X-linked intellectual disability 90
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112041
 * non-syndromic X-linked intellectual disability 91
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112043
 * non-syndromic X-linked intellectual disability 92
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112032
 * non-syndromic X-linked intellectual disability 93
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112045
 * non-syndromic X-linked intellectual disability 96
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112035
 * non-syndromic X-linked intellectual disability 97
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112046
 * non-syndromic X-linked intellectual disability 98
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112044
 * non-syndromic X-linked intellectual disability 99
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112026
 * non-syndromic X-linked intellectual disability ARX-related
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112021
 * nonencapsulated sclerosing carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:5914
 * noninfectious dermatoses of eyelid
 * class of disease
 * blepharitis
 * Human disease
 * DOID:1894
 * noninvasive malignant thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:7214
 * nonossifying fibromyxoid tumor
 * class of disease
 * mesenchymal cell neoplasm fibromyxoid tumor
 * Human disease
 * DOID:8305
 * nonphotosensitive trichothiodystrophy
 * class of disease
 * trichothiodystrophy
 * human disease
 * DOID:0111867
 * nonsyndromic aplasia cutis congenita
 * class of disease
 * skin disease aplasia cutis congenita
 * human disease
 * DOID:0080661
 * nonsyndromic congenital nail disorder
 * class of disease
 * nail disease
 * human disease
 * DOID:0080683
 * nonsyndromic congenital nail disorder 1
 * class of disease
 * nail disease Twenty-nail dystrophy inherited isolated nail anomaly epidermal disease nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080079
 * nonsyndromic congenital nail disorder 2
 * class of disease
 * nail disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080080
 * nonsyndromic congenital nail disorder 5
 * class of disease
 * nail disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080083
 * nonsyndromic congenital nail disorder 6
 * class of disease
 * nail disease autosomal dominant disease nonsyndromic congenital nail disorder
 * Human disease
 * DOID:0080084
 * nonsyndromic congenital nail disorder 7
 * class of disease
 * nail disease epidermal disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080085
 * nonsyndromic congenital nail disorder 9
 * class of disease
 * nail disease inherited isolated nail anomaly autosomal recessive disease nonsyndromic congenital nail disorder
 * Human disease
 * DOID:0080087
 * nontoxic goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13195
 * normal pressure hydrocephalus
 * class of disease
 * communicating hydrocephalus nervous system heredodegenerative disease genetic dementia disease
 * condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure
 * DOID:1572
 * C10.228.140.602.750
 * Normal pressure hydrocephalus
 * normocytic anemia
 * class of disease
 * anemia
 * Human disease
 * DOID:720
 * norwegian scabies
 * class of disease
 * scabies
 * Human disease
 * DOID:14374
 * Crusted scabies
 * Norwegian Scabies in Homeless AIDS Patient.jpg
 * nose disease
 * class of disease
 * upper respiratory tract disease disease
 * respiratory disease
 * DOID:2825
 * C08.460 C09.603
 * Diseases and disorders of the nose and paranasal sinuses
 * notochordal cancer
 * class of disease
 * bone cancer
 * embryonal cancer and bone cancer and mesenchymal cell neoplasm that is located in the notochord
 * DOID:3303
 * nuclear senile cataract
 * class of disease
 * senile cataract nuclear sclerosis
 * Human disease
 * DOID:13963
 * nuclear type mitochondrial complex I deficiency
 * class of disease
 * mitochondrial complex I deficiency
 * human disease
 * DOID:0112065
 * nuclear type mitochondrial complex I deficiency 1
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112074
 * nuclear type mitochondrial complex I deficiency 10
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112075
 * nuclear type mitochondrial complex I deficiency 11
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112089
 * nuclear type mitochondrial complex I deficiency 12
 * class of disease
 * nuclear type mitochondrial complex I deficiency X-linked recessive disease
 * human disease
 * DOID:0112099
 * nuclear type mitochondrial complex I deficiency 13
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112076
 * nuclear type mitochondrial complex I deficiency 14
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112094
 * nuclear type mitochondrial complex I deficiency 15
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112077
 * nuclear type mitochondrial complex I deficiency 16
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112096
 * nuclear type mitochondrial complex I deficiency 17
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112078
 * nuclear type mitochondrial complex I deficiency 18
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112070
 * nuclear type mitochondrial complex I deficiency 19
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112085
 * nuclear type mitochondrial complex I deficiency 2
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112083
 * nuclear type mitochondrial complex I deficiency 20
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112072
 * nuclear type mitochondrial complex I deficiency 21
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112088
 * nuclear type mitochondrial complex I deficiency 22
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112069
 * nuclear type mitochondrial complex I deficiency 23
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112087
 * nuclear type mitochondrial complex I deficiency 24
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112079
 * nuclear type mitochondrial complex I deficiency 25
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112067
 * nuclear type mitochondrial complex I deficiency 26
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112086
 * nuclear type mitochondrial complex I deficiency 27
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112090
 * nuclear type mitochondrial complex I deficiency 28
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112095
 * nuclear type mitochondrial complex I deficiency 29
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112084
 * nuclear type mitochondrial complex I deficiency 3
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112093
 * nuclear type mitochondrial complex I deficiency 30
 * class of disease
 * nuclear type mitochondrial complex I deficiency X-linked recessive disease
 * human disease
 * DOID:0112098
 * nuclear type mitochondrial complex I deficiency 31
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112071
 * nuclear type mitochondrial complex I deficiency 32
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112080
 * nuclear type mitochondrial complex I deficiency 33
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112097
 * nuclear type mitochondrial complex I deficiency 34
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112091
 * nuclear type mitochondrial complex I deficiency 35
 * class of disease
 * autosomal recessive disease mitochondrial complex I deficiency nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112139
 * nuclear type mitochondrial complex I deficiency 4
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112082
 * nuclear type mitochondrial complex I deficiency 5
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112068
 * nuclear type mitochondrial complex I deficiency 6
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112066
 * nuclear type mitochondrial complex I deficiency 7
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112092
 * nuclear type mitochondrial complex I deficiency 8
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112081
 * nuclear type mitochondrial complex I deficiency 9
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112073
 * null-cell leukemia
 * class of disease
 * acute lymphocytic leukemia
 * Human disease
 * DOID:9954
 * nutmeg liver
 * class of disease
 * hepatic vascular disease
 * human disease
 * DOID:13739
 * Congestive hepatopathy
 * nutrition disorder
 * class of disease
 * acquired metabolic disease nutritional and metabolic diseases food-related disease
 * disease that results from excessive or inadequate intake of food and nutrients
 * DOID:374
 * C18.654
 * Nutritional diseases and disorders
 * nutritional deficiency disease
 * class of disease
 * nutrition disorder deficiency
 * human disease
 * DOID:5113
 * C18.654.521.500
 * Diseases and disorders due to nutritional deficiencies
 * nutritional optic neuropathy
 * class of disease
 * optic nerve disease optic neuritis
 * Human disease
 * DOID:1209
 * nystagmus, congenital, autosomal recessive
 * class of disease
 * congenital nystagmus autosomal recessive disease
 * human disease
 * DOID:0111797
 * obsessive-compulsive disorder
 * class of disease
 * anxiety disorder impulse control disorder genetic nervous system disorder genetic disease disease
 * anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)
 * DOID:10933
 * F03.080.600
 * Obsessive–compulsive disorder
 * Obsessive-compulsive disorder world map - DALY - WHO2002.svg
 * obsessive-compulsive personality disorder
 * class of disease
 * personality disorder disease
 * personal perfectionism at the cost of flexibility, openness, efficiency & effect on others
 * DOID:10932
 * F03.675.150
 * Obsessive compulsive personality disorder
 * obstructive hydrocephalus
 * class of disease
 * hydrocephalus
 * abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of an obstruction at any location within the ventricular system that prevents cerebrospinal fluid flowing into the subarachnoid space
 * DOID:14159
 * obstructive jaundice
 * class of disease
 * cholestasis jaundice non-neoplastic bile duct disorder
 * Human disease
 * DOID:13603
 * C23.550.429.500.755 C23.888.885.375.500
 * Obstructive jaundice
 * obstructive lung disease
 * class of disease
 * lung disease disease
 * category of respiratory disease characterized by airway obstruction
 * DOID:2320
 * C08.381.495
 * obstructive nephropathy
 * class of disease
 * kidney disease
 * kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction
 * DOID:0070314
 * obstructive sleep apnea
 * class of disease
 * sleep apnea
 * obstruction of the upper airway during sleep
 * DOID:0050848
 * C08.618.085.852.850 C10.886.425.800.750.850
 * occipital lobe neoplasm
 * class of disease
 * cerebrum cancer
 * Human disease
 * DOID:910
 * occlusion of gallbladder
 * class of disease
 * gallbladder disease
 * Human disease
 * DOID:9714
 * occlusion precerebral artery
 * class of disease
 * cerebrovascular disease
 * human disease
 * DOID:5976
 * occupational asthma
 * class of disease
 * occupational disease asthma environmental induced asthma
 * medical condition caused or exacerbated by the workplace
 * DOID:0080820
 * C08.127.108.495 C08.674.095.495 C20.543.480.680.095.495 C24.102
 * occupational dermatitis
 * class of disease
 * contact dermatitis occupational disease disease
 * Human disease
 * DOID:4404
 * C17.800.174.255.700 C17.800.815.255.700 C24.270
 * ochronosis
 * class of disease
 * connective tissue disease clinical sign disease
 * syndrome caused by the accumulation of homogentisic acid in connective tissues
 * DOID:14223
 * C23.550.744
 * Ochronosis
 * Homogentisic acid.svg
 * ocular albinism
 * class of disease
 * eye disease albinism disease
 * human disease
 * DOID:0050633
 * C11.270.040.090 C16.320.290.040.090 C16.320.565.100.102.090 C16.320.850.080.090 C17.800.621.440.102.090 C17.800.827.080.090 C18.452.648.100.102.090
 * ocular albinism type 2
 * class of disease
 * ocular albinism eye disease X-linked recessive disease
 * Human disease
 * DOID:0050630
 * ocular albinism with sensorineural deafness
 * class of disease
 * ocular albinism Waardenburg's syndrome autosomal dominant disease digenic disease
 * human disease
 * DOID:0090100
 * ocular cancer
 * class of disease
 * sensory system cancer eye tumor eye disease disease
 * type of cancer un the eye
 * DOID:2174
 * ocular hyperemia
 * class of disease
 * conjunctival disease
 * Human disease
 * DOID:1248
 * ocular hypertension
 * class of disease
 * eye disease hypertension disease
 * eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss
 * DOID:9282
 * C11.525
 * ocular hypotension
 * class of disease
 * eye disease hypotension
 * Human disease
 * DOID:790
 * C11.540
 * ocular motility disease
 * class of disease
 * cranial nerve disease eye adnexa disease eye disease
 * human disease
 * DOID:1279
 * C10.228.758 C10.292.562 C11.590
 * ocular tuberculosis
 * class of disease
 * extrapulmonary tuberculosis eye disease tuberculosis
 * Human disease
 * DOID:233 DOID:0070344
 * C01.150.252.289.800 C01.375.354.800 C11.294.354.800
 * oculocutaneous albinism type 2
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13
 * DOID:0070096
 * oculocutaneous albinism type 3
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of TYRP1 on chromosome 9p23
 * DOID:0070097
 * oculocutaneous albinism type 4
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.
 * DOID:0070098
 * oculocutaneous albinism type IA
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.
 * DOID:0070094
 * oculocutaneous albinism type IB
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.
 * DOID:0070095
 * oculocutaneous albinism type V
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA5 on chromosome 4q24
 * DOID:0070099
 * oculoglandular tularemia
 * class of disease
 * tularemia
 * tularemia that results in inflammation of eye and swelling of lymph glands in front of the ear
 * DOID:13226
 * oculogyric crisis
 * class of disease
 * focal dystonia disease
 * focal dystonia that is characterized by a prolonged involuntary upward deviation of the eyes
 * DOID:0050842
 * oculomotor nerve paralysis
 * class of disease
 * third cranial nerve disease paralytic squint
 * Human disease
 * DOID:11550
 * C10.292.562.700 C11.590.436
 * Oculomotor nerve palsy
 * oculopharyngodistal myopathy 4
 * class of disease
 * Oculopharyngodistal myopathy
 * human disease
 * DOID:0081300
 * odontoclasia
 * class of disease
 * dental caries
 * Human disease
 * DOID:11736
 * olecranon bursitis
 * class of disease
 * enthesopathy bursitis disease
 * Human disease
 * DOID:12581
 * Olecranon bursitis
 * Bursitis Elbow WC.JPG
 * olfactory groove meningioma
 * class of disease
 * anterior cranial fossa meningioma
 * Human disease
 * DOID:8057
 * olfactory nerve disease
 * class of disease
 * glossopharyngeal nerve disease encephalopathy
 * Human disease
 * DOID:367
 * C10.292.650
 * oligoasthenoteratospermia
 * class of disease
 * oligospermia Teratospermia asthenozoospermia male infertility
 * A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.
 * DOID:0070311
 * oligodendroglioma
 * class of disease
 * glioma disease
 * type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell
 * DOID:3181
 * C04.557.465.625.600.380.590 C04.557.470.670.380.590 C04.557.580.625.600.380.590
 * Oligodendrogliomas
 * Oligodendroglioma1 high mag.jpg
 * oligohydramnios
 * class of disease
 * placenta disease disease
 * placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion
 * DOID:12215
 * C13.703.560
 * Oligohydramnios
 * oligospermia
 * class of disease
 * male infertility disease
 * semen with abnormally low concentration of sperm
 * DOID:14228
 * C12.294.365.700.508
 * Oligospermia
 * olivopontocerebellar atrophy
 * class of disease
 * neurodegeneration
 * group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives
 * DOID:14784
 * C10.177.575.550.375 C10.228.140.079.612.600 C10.228.140.252.700.650 C10.228.662.550.600 C10.228.854.787.750 C10.574.500.825.650 C10.574.625.600 C16.320.400.780.750
 * omphalocele
 * class of disease
 * congenital disorder abdominal wall defect disease
 * physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac
 * DOID:0060327
 * Omphalocele
 * oncocytic breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:6585
 * oophoritis
 * class of disease symptom or sign
 * ovarian disease inflammatory disease disease
 * human disease
 * DOID:10974
 * C13.351.500.056.630.450 C13.351.500.056.750.500 C19.391.630.450
 * open-angle glaucoma
 * class of disease
 * glaucoma
 * glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage
 * DOID:1067
 * C11.525.381.407
 * ophthalmia neonatorum
 * class of disease
 * gonococcal eye infectious disease bacterial conjunctivitis
 * Human disease
 * DOID:9699
 * ophthalmia nodosa
 * class of disease
 * eye disease
 * Human disease
 * DOID:9722
 * ophthalmomyiasis
 * class of disease
 * myiasis eye disease parasitic eye infection
 * myiasis that involves parasitic infestation of Oestrus ovis larvae in the eye causing severe irritation, edema, and pain
 * DOID:0050268
 * ophthalmoplegia
 * class of disease symptom or sign
 * ocular motility disease paralysis disease
 * Human disease
 * DOID:539
 * C10.292.562.750 C10.597.622.447 C11.590.472 C23.888.592.636.447
 * Ophthalmoparesis
 * opiate dependence
 * class of disease
 * substance dependence opioid use disorder
 * drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance
 * DOID:2559
 * opioid use disorder
 * class of disease
 * addiction substance abuse opioid-related disorders disease
 * substance abuse disorder that involves the recurring use of opioid drugs despite negative consequences
 * DOID:11206
 * Opioid use disorder
 * opportunistic bacterial infectious disease
 * class of disease
 * bacterial infectious disease opportunistic infection
 * bacterial infectious disease that results in infection by bacteria in individuals whose host defense mechanisms have been compromised
 * DOID:0050340
 * opportunistic mycosis
 * class of disease
 * systemic mycosis opportunistic infection
 * A systemic mycosis that results in fungal infection located in human body of immunocompromised individuals, has material basis in Fungi. The organisms invade via the respiratory tract, alimentary tract, or intravascular devices.
 * DOID:2473
 * oppositional defiant disorder
 * class of disease
 * specific developmental disorder emotional and behavioral disorders disease
 * human disorder involving hostility and defiance
 * DOID:0050856
 * F03.625.094.475
 * Oppositional defiant disorder
 * optic atrophy 10
 * class of disease
 * autosomal dominant disease optic atrophy
 * human disease
 * DOID:0111434
 * optic atrophy 11
 * class of disease
 * autosomal recessive isolated optic atrophy autosomal recessive disease optic atrophy
 * human disease
 * DOID:0111436
 * optic atrophy 2
 * class of disease
 * optic atrophy
 * human disease
 * DOID:0111443
 * optic atrophy 4
 * class of disease
 * Kjer's optic neuropathy optic atrophy autosomal dominant disease
 * human disease
 * DOID:0111440
 * optic atrophy 5
 * class of disease
 * Kjer's optic neuropathy optic atrophy autosomal dominant disease
 * human disease
 * DOID:0111438
 * optic atrophy 6
 * class of disease
 * autosomal recessive isolated optic atrophy optic atrophy autosomal recessive disease
 * human disease
 * DOID:0111435
 * optic atrophy 9
 * class of disease
 * autosomal recessive disease optic atrophy
 * human disease
 * DOID:0111442
 * optic disk drusen
 * class of disease
 * optic nerve disease
 * Human disease
 * DOID:13561
 * C10.292.700.450 C11.640.513
 * optic nerve astrocytoma
 * class of disease
 * optic nerve glioma optic nerve disease astrocytoma neuromuscular disease
 * human disease
 * DOID:4991
 * optic nerve disease
 * class of disease
 * cranial nerve disease vision disorder peripheral neuropathy visual pathway disease neuro-ophthalmological disease disease
 * cranial nerve disease that is located in the optic nerve
 * DOID:1891
 * C10.292.700 C11.640
 * Optic neuropathy
 * optic nerve glioma
 * class of disease
 * optic nerve tumor glioma visual pathway glioma brain glioma
 * human disease
 * DOID:4992
 * C04.557.465.625.600.380.795 C04.557.470.670.380.795 C04.557.580.625.600.380.795 C04.588.614.300.600.600 C04.588.614.596.240.240.500 C10.292.225.800.500 C10.292.700.500.500 C10.551.360.500.500 C10.551.775.250.500.500 C11.640.544.500
 * optic neuritis
 * class of disease
 * optic nerve disease eye disease encephalomyelitis disease
 * optic nerve disease that results in inflammation located in optic nerve which may cause a complete or partial loss of vision
 * DOID:1210
 * C10.292.700.550 C11.640.576
 * Optic neuritis
 * optic papillitis
 * class of disease
 * optic neuritis
 * human disease
 * DOID:10175
 * oral cavity carcinoma in situ
 * class of disease
 * in situ carcinoma mouth cancer mouth disease carcinoma in situ of digestive organ
 * Human disease
 * DOID:0050610
 * oral hairy leukoplakia
 * class of disease
 * mouth disease oral mucosa leukoplakia disease
 * mouth disease characterized by a white patch on the lateral sides of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus
 * DOID:0060315
 * C01.925.256.466.313.500 C04.588.443.591.545.500 C04.834.512.513.500 C07.465.565.545.500 C23.300.816.513.500
 * oral leukoedema
 * class of disease
 * mouth disease Leukoedema
 * Human disease
 * DOID:4557
 * C07.465.385
 * oral mucosa leukoplakia
 * class of disease
 * mouth disease leukoplakia
 * Human disease
 * DOID:9655
 * C04.588.443.591.545 C04.834.512.513 C07.465.565.545 C23.300.816.513
 * Oral leukoplakia
 * oral submucous fibrosis
 * class of disease
 * mouth disease rare maxillo-facial surgical disease
 * human disease
 * DOID:5773
 * C07.465.654
 * oral-facial-digital syndrome
 * class of disease
 * syndrome
 * genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene
 * DOID:4501
 * C05.116.099.370.652 C05.660.207.700 C16.131.077.676 C16.131.260.830.670 C16.131.621.207.700 C16.320.180.830.670 C16.320.714
 * orange allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Citrus sinensis plant fruit food product.
 * DOID:0060508
 * orbit embryonal rhabdomyosarcoma
 * class of disease
 * orbit rhabdomyosarcoma embryonal rhabdomyosarcoma
 * Human disease
 * DOID:3258
 * orbit rhabdomyosarcoma
 * class of disease
 * orbit sarcoma
 * Human disease
 * DOID:3259
 * orbital cancer
 * class of disease
 * bone cancer orbit neoplasm orbital disease
 * Human disease
 * DOID:4143
 * orbital cyst
 * class of disease
 * orbital disease
 * Human disease
 * DOID:14233
 * orbital disease
 * class of disease
 * eye adnexa disease bone disease
 * adnexa disease that is located in the eye socket
 * DOID:930
 * C11.675
 * orbital granuloma
 * class of disease
 * chronic orbital inflammation
 * Human disease
 * DOID:10499
 * orbital osteomyelitis
 * class of disease
 * acute orbital inflammation osteomyelitis
 * Human disease
 * DOID:11232
 * orbital periostitis
 * class of disease
 * acute orbital inflammation
 * human disease
 * DOID:11231
 * orbital tenonitis
 * class of disease
 * acute orbital inflammation
 * Human disease
 * DOID:11233
 * orchitis
 * class of disease
 * testicular disease inflammatory disease disease
 * inflammation of the testes
 * DOID:2518
 * C12.294.829.493 C19.391.829.493
 * Orchitis
 * Orkite cok2 pere polets 32 samwinnes.JPG
 * organ system benign neoplasm
 * class of disease
 * benign neoplasm disease of anatomical entity
 * benign neoplasm that is classified by the organ system from which it is arising from
 * DOID:0060085
 * organ system cancer
 * class of disease
 * cancer cancer by anatomical entity
 * cancer that is classified based on the organ it starts in
 * DOID:0050686
 * C04.588
 * organic acidemia
 * class of disease
 * amino acid metabolic disorder
 * amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids
 * DOID:0060159
 * orofacial cleft 1
 * class of disease
 * cleft lip and cleft palate autosomal dominant disease
 * An orofacial cleft characterized by autosomal dominant inheritance that has material basis in variation in chromosome region 6p24.3.
 * DOID:0080395
 * orofacial cleft 10
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in mutation in the SUMO1 gene on chromosome 2q33
 * DOID:0080403
 * orofacial cleft 11
 * class of disease
 * cleft lip and cleft palate
 * human disease
 * DOID:0080404
 * orofacial cleft 12
 * class of disease
 * cleft lip and cleft palate
 * An orofacial cleft that has material basis in variation in the chromosome region 8q24.3.
 * DOID:0080405
 * orofacial cleft 13
 * class of disease
 * cleft lip and cleft palate autosomal dominant disease
 * orofacial cleft characterized by autosomal doninant inhertitance that has material basis in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730
 * DOID:0080406
 * orofacial cleft 14
 * class of disease
 * cleft lip and cleft palate autosomal recessive disease
 * human disease
 * DOID:0080407
 * orofacial cleft 15
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in mutation in the DLX4 gene on chromosome 17q21
 * DOID:0080408
 * orofacial cleft 2
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the chromosome region 2p13
 * DOID:0080396
 * orofacial cleft 3
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the chromosomal region 19q13
 * DOID:0080397
 * orofacial cleft 4
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the 4q21-q31 chromosomal region
 * DOID:0080398
 * orofacial cleft 5
 * class of disease
 * cleft lip and cleft palate
 * human disease
 * DOID:0080399
 * orofacial cleft 6
 * class of disease
 * autosomal dominant disease cleft lip and cleft palate
 * human disease
 * DOID:0080593
 * orofacial cleft 7
 * class of disease
 * cleft lip and cleft palate autosomal recessive disease
 * orofacial cleft that has material basis in by homozygous mutation in the PVRL1 gene on chromosome 11q23
 * DOID:0080400
 * orofacial cleft 8
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in heterozygous mutation in the TP63 gene on chromosome 3q28
 * DOID:0080401
 * orofacial cleft 9
 * class of disease
 * cleft lip and cleft palate
 * An orofacial cleft that has material basis in variation in the chromosome region 13q33.1-q34.
 * DOID:0080402
 * orofaciodigital syndrome VIII
 * class of disease
 * oral-facial-digital syndrome X-linked recessive disease
 * human disease
 * DOID:0060378
 * oromandibular dystonia
 * class of disease
 * focal dystonia lingual-facial-buccal dyskinesia focal, segmental or multifocal dystonia
 * focal dystonia that is characterized by distortions of the mouth and tongue.
 * DOID:0050843
 * oropharyngeal anthrax
 * class of disease
 * gastrointestinal anthrax
 * human disease
 * DOID:0050059
 * orthostatic proteinuria
 * class of disease symptom or sign
 * kidney disease proteinuria
 * Human disease
 * DOID:9617
 * osmotic diarrhea
 * class of disease
 * diarrhea chronic diarrhea
 * Human disease
 * DOID:0050130
 * ossifying fibroma
 * class of disease
 * bone benign neoplasm
 * bone benign neoplasm that is located in the mouth and results in an overgrowth of gingival tissue due to irritation or trauma
 * DOID:180
 * C04.557.450.565.575.400 C04.557.450.565.590.340.360
 * ossifying fibromyxoid tumour
 * class of disease
 * fibromyxoid tumor mesenchymal cell neoplasm
 * human disease
 * DOID:2685
 * osteoarticular tuberculosis
 * class of disease
 * extrapulmonary tuberculosis bone disease
 * extrapulmonary tuberculosis that results in formation of lesions located in bone
 * DOID:1639
 * C01.150.252.410.040.552.846.617.525 C01.160.886 C05.116.165.886
 * osteoblastoma
 * class of disease
 * bone benign neoplasm osteogenic neoplasm disease
 * Human disease
 * DOID:0060098
 * C04.557.450.565.575.600
 * Osteoblastoma
 * Osteoblastoma - high mag.jpg
 * osteochondrodysplasia
 * class of disease
 * bone development disease
 * bone development disease that results in defective development of cartilage or bone
 * DOID:2256
 * C05.116.099.708 C16.320.728
 * Osteochondrodysplasias
 * osteochondrosis
 * class of disease symptom or sign
 * ischemic bone disease disease
 * ischemic bone disease that results in necrosis followed by regrowth in children and teens located in bone
 * DOID:8125
 * C05.116.821
 * Osteochondrosis
 * osteoclast-like giant cell neoplasm of the pancreas
 * class of disease
 * pancreatic ductal adenocarcinoma undifferentiated pancreatic carcinoma
 * Human disease
 * DOID:7718
 * osteogenesis imperfecta 21
 * class of disease
 * osteogenesis imperfecta
 * human disease
 * DOID:0112201
 * osteogenesis imperfecta type 1
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by bone fragility and blue sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110334
 * osteogenesis imperfecta type 16
 * class of disease
 * osteogenesis imperfecta
 * osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
 * DOID:0110345
 * osteogenesis imperfecta type 18
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111848
 * osteogenesis imperfecta type 20
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111849
 * osteogenesis imperfecta type 3
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has material basis in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110339
 * osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
 * class of disease
 * osteogenesis imperfecta dentinogenesis imperfecta blue sclera
 * osteogenesis imperfecta found in a single South African family
 * DOID:0110335
 * osteomalacia
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone
 * DOID:10573
 * C05.116.198.816.640 C18.452.104.816.640 C18.452.174.845.640 C18.654.521.500.133.770.734.640
 * Calcitriol.svg
 * osteomyelitis
 * class of disease
 * bone inflammation disease infectious disease disease
 * bone inflammation disease that has material basis in infection located in bone or located in bone marrow
 * DOID:1019
 * C01.160.495 C05.116.165.495
 * Osteomyelitis
 * osteonecrosis
 * class of disease symptom or sign
 * necrosis ischemic bone disease disease
 * bone death caused when the bone no longer receives blood supply
 * DOID:10159
 * C05.116.852 C23.550.717.732
 * Aseptic osteonecrosis
 * Head of femur avascular necrosis.jpg
 * osteopoikilosis
 * class of disease
 * osteosclerosis
 * osteosclerosis that results in numerous bone islands located in skeleton
 * DOID:11991
 * C05.116.099.708.702.685 C17.300.705
 * Osteopoikilosis
 * osteoporosis
 * class of disease
 * bone resorption disease disease
 * bone resorption disease characterized by the thinning of bone tissue and decreased mechanical strength
 * DOID:11476
 * C05.116.198.579 C18.452.104.579
 * Osteoporosis
 * Osteoporosis -- Smart-Servier.jpg
 * osteosarcoma
 * class of disease
 * bone cancer cell type cancer bone sarcoma osteogenic neoplasm disease childhood cancer
 * bone cancer that is located in bone that has material basis in cells of mesenchymal origin
 * DOID:3347
 * C04.557.450.565.575.650 C04.557.450.795.620
 * Osteosarcoma
 * Osteosarcoma.jpg
 * osteosarcoma arising in bone Paget's disease
 * class of disease
 * bone osteosarcoma mammary Paget's disease
 * Human disease
 * DOID:7542
 * osteosclerosis
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that results in abnormal elevated bone density or mass
 * DOID:4254
 * C05.116.099.708.702
 * ScleroticmetastaticdiseasePelvis.png
 * otomycosis
 * class of disease symptom or sign
 * otitis externa dermatomycosis disease
 * human disease
 * DOID:0050147
 * C01.150.703.658 C09.218.736
 * Otomycosis
 * Otomycosis.jpg
 * otopalatodigital syndrome spectrum disorder
 * class of disease
 * bone development disease
 * DOID:0111782
 * otosclerosis
 * class of disease
 * inner ear disease disease
 * otitis interna characterized by an abnormal bone growth in the middle ear
 * DOID:12185
 * C09.218.768
 * Otosclerosis
 * Gray919.png
 * otospondylomegaepiphyseal dysplasia, autosomal dominant
 * class of disease
 * osteochondrodysplasia autosomal dominant disease
 * human disease
 * DOID:0080677
 * outlet dysfunction constipation
 * class of disease
 * constipation
 * Human disease
 * DOID:2088
 * ovarian Brenner tumor
 * class of disease
 * ovarian benign neoplasm
 * ovarian benign neoplasm that has material basis in the surface epithelium of the ovary
 * DOID:2636
 * Brenner tumour
 * ovarian Wilms' cancer
 * class of disease
 * ovarian cancer
 * malignant neoplasm of ovary and nephroblastoma that is located in the ovaries
 * DOID:2153
 * ovarian angiosarcoma
 * class of disease
 * angiosarcoma ovary sarcoma sarcoma ovarian cancer
 * human disease
 * DOID:4527
 * ovarian benign neoplasm
 * class of disease
 * female reproductive organ benign neoplasm ovarian neoplasm endocrine organ benign neoplasm ovarian disease
 * human disease
 * DOID:0060112
 * Benign neoplasms of the ovary
 * ovarian biphasic or triphasic teratoma
 * class of disease
 * ovarian germ cell teratoma
 * Human disease
 * DOID:6232
 * ovarian cancer
 * class of disease
 * female reproductive organ cancer ovarian neoplasm ovarian disease endocrine gland cancer rare genetic endocrine disease inherited gynecological tumor disease
 * female reproductive organ cancer that is located in the ovary
 * DOID:2394
 * Ovarian cancer
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian carcinoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinoma
 * human disease
 * DOID:4001
 * ovarian carcinosarcoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinosarcoma mixed Müllerian tumor
 * Human disease
 * DOID:6170
 * ovarian clear cell adenocarcinoma
 * class of disease
 * ovary adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5304
 * ovarian clear cell adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5897
 * ovarian clear cell cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma ovarian clear cell adenocarcinoma
 * Human disease
 * DOID:7438
 * ovarian clear cell cystadenofibroma
 * class of disease
 * ovarian clear cell adenofibroma clear cell cystadenofibroma
 * Human disease
 * DOID:5896
 * ovarian clear cell malignant adenofibroma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:6554
 * ovarian cyst
 * class of disease
 * ovarian disease ovarian neoplasm disease
 * fluid-filled sac in the ovary
 * DOID:5119
 * C04.182.612 C13.351.500.056.630.580 C19.391.630.580
 * Ovarian cysts
 * Benign Ovarian Cyst.jpg
 * ovarian cystadenocarcinoma
 * class of disease
 * ovary adenocarcinoma cystadenocarcinoma ovarian cystadenoma
 * human disease
 * DOID:3605
 * ovarian cystadenoma
 * class of disease
 * ovarian benign neoplasm benign epithelial neoplasm
 * human disease
 * DOID:3269
 * ovarian cystic teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:5118
 * Mature cystic teratoma of ovary
 * ovarian disease
 * class of disease
 * female reproductive system disease gonadal disease adnexal disease
 * Human disease
 * DOID:1100
 * C13.351.500.056.630 C19.391.630
 * Diseases and disorders of ovaries
 * ovarian dysfunction
 * class of disease
 * ovarian disease
 * Human disease
 * DOID:1414
 * ovarian dysgenesis 1
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16
 * DOID:0080493
 * ovarian dysgenesis 4
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MCM9 gene on chromosome 6q22
 * DOID:0080496
 * ovarian dysgenesis 5
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the SOHLH1 gene on chromosome 9q34
 * DOID:0080497
 * ovarian dysgenesis 6
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the NUP107 gene on chromosome 12q15
 * DOID:0080498
 * ovarian dysgenesis 7
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MRPS22 gene on chromosome 3q23
 * DOID:0080499
 * ovarian dysgenesis 8
 * class of disease
 * 46 XX gonadal dysgenesis autosomal dominant disease
 * 46 XX gonadal dysgenesis that has material basis in heterozygous mutation in the ESR2 gene on chromosome 14q23
 * DOID:0080500
 * ovarian embryonal carcinoma
 * class of disease
 * embryonal carcinoma malignant non-dysgerminomatous germ cell tumor of ovary ovarian cancer
 * embryonal carcinoma that is located in the ovary
 * DOID:5681
 * ovarian endodermal sinus tumor
 * class of disease
 * ovarian primitive germ cell tumor malignant non-dysgerminomatous germ cell tumor of ovary endodermal sinus tumor
 * Human disease
 * DOID:5350
 * ovarian endometrial cancer
 * class of disease
 * surface epithelial-stromal tumor Endometrioid tumor female reproductive endometrioid cancer
 * ovary epithelial cancer that has material basis in the endometrium and is located in the ovary
 * DOID:6212
 * ovarian endometrioid adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5480
 * ovarian endometrioid cystadenofibroma
 * class of disease
 * ovarian endometrioid adenofibroma cystadenofibroma
 * Human disease
 * DOID:7411
 * ovarian endometrioid cystadenoma
 * class of disease
 * ovarian cystadenoma
 * Human disease
 * DOID:7191
 * ovarian endometrioid malignant adenofibroma
 * class of disease
 * ovarian carcinosarcoma malignant adenofibroma
 * Human disease
 * DOID:6445
 * ovarian endometrioid stromal sarcoma
 * class of disease
 * ovary sarcoma
 * Human disease
 * DOID:5169
 * ovarian fetiform teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6314
 * ovarian germ cell monodermal and highly specialized teratoma
 * class of disease
 * monodermal teratoma
 * Human disease
 * DOID:2641
 * ovarian germ cell neoplasm
 * class of disease
 * ovarian neoplasm germ cell tumor germ cell and embryonal neoplasms ovarian cancer
 * benign or malignant ovarian tumor that originates in the germ (egg) cells of the ovary
 * DOID:2156
 * Germ cell neoplasms
 * ovarian germ cell teratoma
 * class of disease
 * ovarian germ cell neoplasm teratoma gonadal teratoma female reproductive organ cancer
 * Human disease
 * DOID:5567
 * Ovarian teratomas
 * Teratoma Ovary 4x.jpg
 * ovarian gonadoblastoma
 * class of disease
 * ovarian benign neoplasm gonadoblastoma
 * Human disease
 * DOID:3578
 * ovarian large-cell neuroendocrine carcinoma
 * class of disease
 * ovarian carcinoma familiar ovarian carcinoma inherited neuroendocrine tumor large cell neuroendocrine carcinoma
 * Human disease
 * DOID:4555
 * ovarian lymphoma
 * class of disease
 * ovarian cancer lymphoma
 * Human disease
 * DOID:2150
 * ovarian malignant mesothelioma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:2143
 * ovarian melanoma
 * class of disease
 * ovarian cancer
 * ovarian cancer that has material basis in melanoctyes
 * DOID:0050928
 * ovarian mesodermal adenosarcoma
 * class of disease
 * ovarian carcinosarcoma adenosarcoma
 * adenosarcoma and malignant ovarian endometroid tumorthat is located in the ovary
 * DOID:4115
 * ovarian mixed germ cell neoplasm
 * class of disease
 * ovarian primitive germ cell tumor mixed germ cell cancer
 * Human disease
 * DOID:5936
 * ovarian mucinous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma malignant ovarian mucinous tumor mucinous adenocarcinoma
 * human disease
 * DOID:3606
 * ovarian mucinous adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * human disease
 * DOID:6469
 * ovarian mucinous cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma mucinous cystadenocarcinoma ovarian mucinous adenocarcinoma
 * Human disease
 * DOID:3604
 * ovarian mucinous cystadenofibroma
 * class of disease
 * ovarian mucinous adenofibroma mucinous cystadenofibroma
 * Human disease
 * DOID:7013
 * ovarian mucinous malignant adenofibroma
 * class of disease
 * malignant ovarian mucinous tumor malignant adenofibroma ovarian mucinous neoplasm
 * Human disease
 * DOID:6278
 * ovarian mucinous neoplasm
 * class of disease
 * surface epithelial-stromal tumor mucinous tumor
 * Human disease
 * DOID:6067
 * Ovarian mucinous tumors
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian papillary cystadenoma
 * class of disease
 * ovarian papillary neoplasm papillary adenoma ovarian cystadenoma
 * Human disease
 * DOID:6405
 * ovarian papillary neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:6214
 * ovarian primitive germ cell tumor
 * class of disease
 * malignant ovarian germ cell neoplasm
 * Human disease
 * DOID:5351
 * ovarian serous adenofibroma
 * class of disease
 * ovarian benign neoplasm serous adenofibroma
 * Human disease
 * DOID:5474
 * ovarian serous carcinoma
 * class of disease
 * ovarian carcinoma serous carcinoma ovarian serous tumor
 * ovarian carcinoma that has material basis in the lining of the ovary and produces a serum-like fluid
 * DOID:0050933
 * Ovarian serous carcinoma
 * ovarian serous cystadenofibroma
 * class of disease
 * ovarian serous adenofibroma cystadenofibroma
 * Human disease
 * DOID:7320
 * ovarian serous cystadenoma
 * class of disease
 * serous cystadenoma ovarian benign neoplasm ovarian cystadenocarcinoma serous cystadenocarcinoma ovarian cystadenoma ovarian serous tumor
 * ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed
 * DOID:5746 DOID:3914
 * C04.557.470.035.320.240 C04.557.470.590.485.240
 * Ovarian serous cystadenoma
 * Ovarian serous cystadenoma - alt -- low mag.jpg
 * ovarian sex cord-stromal tumor
 * class of disease
 * sex cord-gonadal stromal tumor
 * A benign or malignant neoplasm that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts. Representative examples include thecoma, fibroma, Sertoli cell tumor, and granulosa cell tumor.
 * DOID:0080369
 * ovarian small cell carcinoma
 * class of disease
 * ovarian carcinoma small cell carcinoma
 * Human disease
 * DOID:6179
 * ovarian solid teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6315
 * ovarian squamous cell carcinoma
 * class of disease
 * ovarian squamous cell neoplasm squamous cell carcinoma ovarian cancer
 * Human disease
 * DOID:5531
 * ovarian squamous cell neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:5532
 * ovarian surface papilloma
 * class of disease
 * ovarian papillary neoplasm
 * Human disease
 * DOID:6407
 * ovary adenocarcinoma
 * class of disease
 * ovarian carcinoma adenocarcinoma
 * ovarian carcinoma that derives from epithelial cells of glandular origin
 * DOID:3713
 * Adenocarcinomas of the ovary
 * [[File:Metastatic ovarian adenocarcinoma- Pleural fluid cell block Case 168 (5494503444).jpg|center|64px]]
 * ovary leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5263
 * ovary mixed epithelial carcinoma
 * class of disease
 * ovarian carcinoma
 * Human disease
 * DOID:6898 DOID:6899
 * ovary neuroendocrine neoplasm
 * class of disease
 * ovarian cancer neuroendocrine tumor
 * Human disease
 * DOID:3002
 * ovary papillary carcinoma
 * class of disease
 * ovarian papillary neoplasm ovarian carcinoma
 * Human disease
 * DOID:6408
 * ovary rhabdomyosarcoma
 * class of disease
 * ovary sarcoma rhabdomyosarcoma
 * Human disease
 * DOID:4059
 * ovary sarcoma
 * class of disease
 * ovarian cancer sarcoma
 * human disease
 * DOID:2146
 * ovary serous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma ovarian serous carcinoma
 * ovary adenocarcinoma that derives from the lining of a cavity that produces a serum-like fluid (a serous cavity)
 * DOID:5744
 * Serous adenocarcinoma of the ovary
 * overhydrated hereditary stomatocytosis
 * class of disease
 * macrocytic anemia autosomal dominant disease hereditary stomatocytosis
 * human disease
 * DOID:0111562
 * overnutrition
 * class of disease
 * nutrition disorder malnutrition
 * form of malnutrition in which the intake of nutrients is oversupplied
 * DOID:654
 * C18.654.726
 * ovine and caprine brucellosis
 * class of disease
 * brucellosis
 * A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.
 * DOID:14456
 * oxirane allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger oxirane
 * DOID:0040082
 * oxyphilic adenoma
 * class of disease
 * endocrine organ benign neoplasm oncocytic neoplasm benign epithelial neoplasm disease
 * Human disease
 * DOID:5389
 * C04.557.470.035.140
 * Oncocytoma
 * Parotid gland oncocytoma - very high mag.jpg
 * oxyphilic endometrial endometrioid adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:6865
 * pain agnosia
 * class of disease
 * agnosia absence of pain sensation
 * agnosia that is a loss of the ability to perceive and process pain
 * DOID:0060145
 * pain disorder
 * class of disease
 * somatoform disorder disease pain
 * somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.
 * DOID:0060164
 * palindromic rheumatism
 * class of disease
 * syndrome arthritis
 * human disease
 * DOID:1166
 * palladium allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis metal allergy
 * allergic contact dermatitis that has allergic trigger palladium
 * DOID:0040055
 * palmoplantar keratosis
 * class of disease
 * keratosis foot diseases epidermal disease disease
 * keratosis characterized by abnormal thickening of the palms and the soles
 * DOID:3390
 * C16.320.850.475 C17.800.428.435 C17.800.827.475
 * Palmoplantar keratodermas
 * pancreas disease
 * class of disease
 * endocrine system disease
 * endocrine system disease that is located in the pancreas
 * DOID:26
 * C06.689
 * Diseases and disorders of pancreas
 * pancreas lymphoma
 * class of disease
 * pancreatic cancer lymphoma
 * human disease
 * DOID:1792
 * pancreas sarcoma
 * class of disease
 * pancreatic cancer sarcoma
 * pancreatic cancer that is located in the pancreas and that arises from transformed cells of mesenchymal origin
 * DOID:1796
 * pancreatic ACTH hormone producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:7697
 * pancreatic acinar cell adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma Acinar cell carcinoma of the pancreas acinar adenocarcinoma
 * pancreatic adenocarcinoma that has material basis in cells with morphological resemblance to acinar cells and is associated with increased serum lipase
 * DOID:5742
 * pancreatic adenocarcinoma
 * class of disease
 * pancreatic carcinoma adenocarcinoma
 * pancreatic carcinoma that derives from epithelial cells of glandular origin
 * DOID:4074
 * Adenocarcinomas of the pancreas
 * [[File:Metastatic pancreatic adenocarcinoma with lepidic growth pattern Case 280 (9840005374).jpg|center|64px]]
 * pancreatic cancer
 * class of disease
 * endocrine gland cancer pancreas disease pancreatic neoplasm gastrointestinal system cancer disease
 * endocrine gland cancer located in the pancreas
 * DOID:1793
 * Pancreatic cancer
 * MBq cystic-carcinoma-pancreas.jpg
 * pancreatic carcinoma
 * class of disease
 * pancreatic cancer carcinoma gastrointestinal carcinoma
 * pancreas cancer that derives from epithelial cells located in the pancreas
 * DOID:4905
 * pancreatic cholera
 * class of disease
 * endocrine pancreas disease
 * Human disease
 * DOID:6977
 * pancreatic colloid cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma mucinous cystadenocarcinoma
 * Human disease
 * DOID:7234
 * pancreatic cystadenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma cystadenocarcinoma
 * Human disease
 * DOID:4073
 * pancreatic cystadenoma
 * class of disease
 * benign neoplasm of exocrine pancreas endocrine organ benign neoplasm benign neoplasm of pancreas gastrointestinal system benign neoplasm pancreas disease
 * human disease
 * DOID:3918
 * pancreatic delta cell neoplasm
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:4433
 * pancreatic ductal adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * pancreatic adenocarcinoma that derives from pancreatic duct cells
 * DOID:3498
 * pancreatic ductal carcinoma
 * class of disease
 * pancreatic cancer ductal carcinoma pancreatic carcinoma
 * most common cancer of the pancreas
 * DOID:3587
 * C04.557.470.200.025.232.750 C04.557.470.615.132.750 C04.588.274.761.750 C04.588.322.475.750 C06.301.761.750 C06.689.667.625 C19.344.421.750
 * pancreatic foamy gland adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * Human disease
 * DOID:7577
 * pancreatic gastrinoma
 * class of disease
 * islet cell tumor functional pancreatic neuroendocrine tumor
 * Human disease
 * DOID:5580
 * pancreatic intraductal papillary-colloid carcinoma
 * class of disease
 * pancreatic adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7574
 * pancreatic intraductal papillary-mucinous adenoma
 * class of disease
 * pancreatic intraductal papillary-mucinous neoplasm adenoma of pancreas gastrointestinal system benign neoplasm adenoma
 * Human disease
 * DOID:7851
 * pancreatic intraductal papillary-mucinous neoplasm
 * class of disease
 * cancer of exocrine pancreas
 * Human disease
 * DOID:7575
 * pancreatic invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma
 * Human disease
 * DOID:8150
 * pancreatic invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * Human disease
 * DOID:7236
 * pancreatic mucinous cystadenoma
 * class of disease
 * mucinous cystadenoma pancreatic cystadenoma
 * human disease
 * DOID:7235
 * pancreatic mucinous ductal ectasia
 * class of disease
 * pancreas disease
 * Human disease
 * DOID:13313
 * pancreatic non-functioning delta cell tumor
 * class of disease
 * pancreatic delta cell neoplasm non-functioning pancreatic endocrine tumor
 * Human disease
 * DOID:7840
 * pancreatic non-invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7685
 * pancreatic non-invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * human disease
 * DOID:7237
 * pancreatic serous cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma serous cystadenocarcinoma pancreatic serous cystic neoplasm
 * Human disease
 * DOID:5751
 * pancreatic serous cystadenoma
 * class of disease
 * serous cystadenoma pancreatic cystadenoma disease
 * human disease
 * DOID:3917
 * Serous cystadenoma pancreas
 * pancreatic serous cystic neoplasm
 * class of disease
 * pancreatic exocrine neoplasm Serous tumour cystic lesions of the pancreas cancer of exocrine pancreas
 * Human disease
 * DOID:3919
 * Serous cystic neoplasms of the pancreas
 * pancreatic signet ring cell adenocarcinoma
 * class of disease
 * pancreatic ductal adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:3497
 * pancreatic solid pseudopapillary carcinoma
 * class of disease
 * pancreatic carcinoma
 * pancreatic carcinoma that is characterized by its papillary architecture
 * DOID:6827
 * pancreatic somatostatinoma
 * class of disease
 * islet cell tumor pancreatic delta cell neoplasm somatostatinoma
 * Human disease
 * DOID:4432
 * pancreatic squamous cell carcinoma
 * class of disease
 * pancreatic cancer squamous cell carcinoma
 * squamous cell carcinoma located in the pancreas
 * DOID:0080323
 * pancreatic steatorrhea
 * class of disease
 * pancreas disease steatorrhea
 * Human disease
 * DOID:10610
 * pancreatic vasoactive intestinal peptide producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:5741
 * pancreatoblastoma
 * class of disease
 * pancreatic carcinoma rare epithelial tumor of pancreas disease
 * Human disease
 * DOID:6823
 * pancytopenia
 * class of disease
 * anemia cytopenia disease
 * medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets
 * DOID:12450
 * C15.378.243.875
 * panhypopituitarism, X-linked
 * class of disease
 * panhypopituitarism X-linked disease
 * human disease
 * DOID:0111779
 * panic disorder
 * class of disease
 * anxiety disorder disease
 * anxiety disorder characterized by reoccurring unexpected panic attacks
 * DOID:594
 * F03.080.700
 * Panic disorder
 * Panic attack.jpg
 * panniculitis
 * class of disease
 * fibromyalgia connective tissue disease skin disease disease
 * Inflammation of the subcutaneous adipose tissue
 * DOID:1526
 * C17.300.710 C17.800.566
 * Panniculitis
 * An introduction to dermatology (1905) erythema induratum 2.jpg
 * panuveitis
 * class of disease
 * uveitis
 * Human disease
 * DOID:12030
 * C11.941.879.780
 * papillary adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue
 * DOID:3112
 * C04.557.470.200.025.085
 * papillary adenofibroma
 * class of disease
 * adenofibroma
 * biphasic polypoid neoplasm characterized by the presence of papillary projections that are lined by epithelial cells and fibrotic stroma
 * DOID:5479
 * papillary adenoma
 * class of disease
 * glandular cell epithelial neoplasm adenoma
 * Human disease
 * DOID:3172
 * papillary carcinoma
 * class of disease
 * carcinoma
 * carcinoma derived from epithelial cells with finger-like projections
 * DOID:3113
 * C04.557.470.200.360 C04.557.470.700.360
 * papillary conjunctivitis
 * class of disease
 * conjunctivitis
 * Human disease
 * DOID:2458
 * papillary craniopharyngioma
 * class of disease
 * craniopharyngioma
 * Human disease
 * DOID:3847
 * papillary cystadenocarcinoma
 * class of disease
 * cystadenocarcinoma papillary cystic tumor
 * cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with cysts and papillary endophytic projections
 * DOID:3110
 * C04.557.470.200.025.480.230 C04.557.470.590.480.230
 * papillary eccrine adenoma
 * class of disease
 * eccrine sweat gland neoplasm papillary adenoma
 * Human disease
 * DOID:5446
 * papillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5505
 * papillary extrahepatic bile duct adenocarcinoma
 * class of disease
 * extrahepatic bile duct adenocarcinoma
 * Human disease
 * DOID:6931
 * papillary follicular thyroid adenocarcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:3968
 * C04.557.470.200.025.060.225 C04.557.470.200.025.085.225
 * papillary hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:5439
 * Papillary hidradenoma
 * Papillary hidradenoma - very high mag.jpg
 * papillary meningioma of the cerebellum
 * class of disease
 * cerebellum cancer rhabdoid meningioma papillary meningioma brain meningioma
 * Human disease
 * DOID:5057
 * papillary pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8193
 * papillary renal cell carcinomas
 * class of disease
 * renal cell carcinoma
 * renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors
 * DOID:4465
 * [[File:Histopathology of papillary renal cell carcinoma type 1, grade 2, with variable density.jpg|center|64px]]
 * papillary serous adenocarcinoma
 * class of disease
 * papillary adenocarcinoma
 * papillary adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures with psammoma bodies
 * DOID:2632
 * papillary squamous carcinoma
 * class of disease
 * squamous cell carcinoma papillary carcinoma
 * Human disease
 * DOID:4385
 * papillary thymic adenocarcinoma
 * class of disease
 * thymus adenocarcinoma
 * Human disease
 * DOID:5595
 * papillary thyroid cancer
 * class of disease
 * thyroid carcinoma papillary carcinoma differentiated thyroid carcinoma
 * thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer
 * DOID:3969
 * C04.557.470.200.025.085.612 C04.588.322.894.400 C04.588.443.915.400 C19.344.894.400 C19.874.788.400
 * Thyroid papillary carcinoma
 * papillary transitional carcinoma
 * class of disease
 * transitional cell carcinoma
 * transitional cell carcinoma that has several papillary fronds with central fibrovascular core lined by transitional type epithelium
 * DOID:4012
 * Urothelial papillary carcinoma
 * papillary urothelial neoplasm of low malignant potential
 * class of disease
 * bladder papillary transitional cell neoplasm urinary tract non-invasive transitional cell neoplasm papillary urothelial lesion
 * human disease
 * DOID:6239
 * papilledema
 * class of disease
 * optic nerve disease disease
 * Human disease
 * DOID:146
 * C10.292.700.900 C11.640.710
 * Papilledema
 * Papilledema.jpg
 * papilloma
 * class of disease
 * benign neoplasms by histologic type papillary tumor disease
 * cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue
 * DOID:2615
 * C04.557.470.700.600
 * Papillomas
 * parachordoma
 * class of disease
 * mesenchymal cell neoplasm
 * Human disease
 * DOID:2647
 * paralytic ileus
 * class of disease
 * bowel obstruction ileus
 * Human disease
 * DOID:8442
 * Paralytic ileus
 * paralytic lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:12958
 * paralytic poliomyelitis
 * class of disease
 * poliomyelitis central nervous system disease
 * Human disease
 * DOID:0050515
 * paralytic squint
 * class of disease
 * strabismus cranial nerve palsy
 * Human disease
 * DOID:10863
 * parameningeal embryonal rhabdomyosarcoma
 * class of disease
 * embryonal rhabdomyosarcoma
 * embryonal rhabdomyosarcoma located in the parameningeal region
 * DOID:0060338
 * parametritis
 * class of disease
 * pelvic inflammatory diseases inflammatory disease uterine disease
 * Human disease
 * DOID:1260
 * C13.351.500.056.750.750
 * parametrium malignant neoplasm
 * class of disease
 * uterine adnexa cancer broad ligament malignant neoplasm
 * Human disease
 * DOID:11746
 * paramyotonia congenita of Von Eulenburg
 * class of disease
 * neuromuscular disease autosomal dominant disease paramyotonia congenita
 * human disease
 * DOID:0111538
 * paranasal sinus disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:1352
 * C08.460.692 C09.603.692
 * paranasal sinus lymphoma
 * class of disease
 * paranasal sinus cancer lymphoma
 * human disease
 * DOID:1355
 * paranasal sinus neoplasm
 * class of disease
 * respiratory tract neoplasm paranasal sinus disease respiratory system benign neoplasm
 * human disease
 * DOID:1350
 * C04.588.443.665.650.693 C08.460.669.693 C08.460.692.503 C08.785.600.693 C09.603.669.693 C09.603.692.503 C09.647.685.693
 * Neoplasms of paranasal sinuses
 * paranasal sinus sarcoma
 * class of disease
 * paranasal sinus cancer sarcoma
 * sarcoma and malignant tumor of nasal sinuses that is located in the paranasal sinus
 * DOID:1362
 * paraneoplastic pemphigus
 * class of disease
 * pemphigus
 * human disease
 * DOID:0080852
 * paraneoplastic polyneuropathy
 * class of disease
 * inflammatory and toxic neuropathy peripheral neuropathy paraneoplastic neurologic syndrome
 * Human disease
 * DOID:8681
 * C04.588.614.550.700 C04.730.856.700 C10.574.781.850 C10.668.829.800.662
 * paranoid personality disorder
 * class of disease
 * personality disorder disease
 * mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others
 * DOID:10938
 * F03.675.600
 * Paranoid personality disorder
 * parapharyngeal meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:8216
 * paraphilia
 * class of disease
 * psychosexual disorder sexual and gender disorder disease
 * experience of intense sexual arousal to atypical objects, situations, or individuals
 * DOID:0060044
 * F03.657
 * Paraphilias
 * Martin van Maele - La Comtesse au fouet 01.jpg
 * paraphimosis
 * class of disease
 * phimosis disease
 * medical condition in which the foreskin of a penis becomes trapped behind the glans penis
 * DOID:5334
 * C12.294.494.684.587
 * Paraphimosis
 * Paraphimosis.jpg
 * paraplegia
 * class of disease symptom or sign
 * central nervous system disease paralysis disease
 * impairment in motor or sensory function of the lower extremities
 * DOID:607
 * C10.597.622.669 C23.888.592.636.637
 * Paraplegia
 * parapsoriasis
 * class of disease
 * psoriasis disease
 * Human disease
 * DOID:9088
 * C17.800.859.575
 * parasagittal meningioma
 * class of disease
 * cerebral convexity meningioma
 * Human disease
 * DOID:6869
 * parasitic Ichthyosporea infectious disease
 * class of disease
 * parasitic infectious diseases
 * parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals
 * DOID:0050291
 * C03.600
 * parasitic conjunctivitis
 * class of disease
 * chronic conjunctivitis parasitic eye infection
 * Human disease
 * DOID:13341
 * parasitic eyelid infestation
 * class of disease
 * blepharitis parasitic eye infection
 * Human disease
 * DOID:13823
 * parasitic protozoa infectious disease
 * class of disease
 * parasitic infectious diseases disease
 * parasitic disease caused by a protozoan
 * DOID:2789
 * C01.610.752
 * paratesticular lipoma
 * class of disease
 * reproductive organ benign neoplasm lipoma
 * Human disease
 * DOID:10207
 * parathyroid adenoma
 * class of disease
 * parathyroid neoplasm benign parathyroid gland neoplasm benign neoplasms by histologic type adenoma disease
 * Human disease
 * DOID:7608
 * Parathyroid adenoma
 * parathyroid gland disease
 * class of disease
 * endocrine system disease
 * endocrine disease
 * DOID:11201
 * C19.642
 * parathyroid oncocytic adenoma
 * class of disease
 * parathyroid adenoma oxyphilic adenoma
 * Human disease
 * DOID:7611
 * parathyroid transitional clear cell adenoma
 * class of disease
 * parathyroid adenoma
 * Human disease
 * DOID:7609
 * paraurethral gland cancer
 * class of disease
 * female reproductive organ cancer paraurethral gland neoplasm
 * Human disease
 * DOID:14059
 * paraurethral gland neoplasm
 * class of disease
 * urethral benign neoplasm
 * Human disease
 * DOID:2139
 * parenchymatous neurosyphilis
 * class of disease
 * tertiary neurosyphilis
 * Human disease
 * DOID:0050490
 * parietal lobe ependymoma
 * class of disease
 * parietal lobe malignant neoplasm ependymoma
 * parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain
 * DOID:0050903
 * paronychia
 * class of disease
 * nail disease disease
 * bacterial or fungal nail infection of the hand or foot
 * DOID:13117
 * C01.539.800.460 C17.800.529.639 C17.800.838.486
 * Paronychia (disease)
 * Paronychia.jpg
 * parotid disease
 * class of disease
 * salivary gland disease
 * Human disease
 * DOID:10302
 * C07.465.815.470
 * Diseases and disorders of parotid glands
 * parotitis
 * class of disease
 * parotid disease inflammatory disease sialadenitis disease
 * parotid disease characterized by the inflammation of one or both parotid glands
 * DOID:10301
 * C07.465.815.470.800 C07.465.815.793.500
 * parovarian cyst
 * class of disease
 * female reproductive system disease embryonic cyst of fallopian tube
 * Human disease
 * DOID:4333
 * C04.182.668 C23.300.306.500
 * paroxysmal nonkinesigenic dyskinesia 2
 * class of disease
 * Paroxysmal dyskinesia dystonia genetic disease
 * human disease
 * DOID:0090047
 * pars planitis
 * class of disease
 * intermediate uveitis chorioretinitis ciliary body disease rare genetic eye disease disease
 * Human disease
 * DOID:12731
 * C11.941.160.478.700 C11.941.879.780.900.300.659 C11.941.879.900.500
 * parthenolide allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger parthenolide
 * DOID:0040072
 * partial androgen insensitivity syndrome
 * class of disease
 * X-linked recessive disease androgen insensitivity syndrome
 * medical condition
 * DOID:0080776
 * partial arterial retinal occlusion
 * class of disease
 * retinal artery occlusion
 * Human disease
 * DOID:14522
 * partial circumpapillary choroid dystrophy
 * class of disease
 * hereditary choroidal atrophy
 * human disease
 * DOID:9811
 * partial lipodystrophy
 * class of disease
 * lipodystrophy
 * lipodystrophy that is characterized by partial loss of adipose tissue
 * DOID:0080299
 * partial motor epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3327
 * C10.228.140.490.360.272
 * partial optic atrophy
 * class of disease
 * optic atrophy
 * human disease
 * DOID:10631
 * partial pancreatic agenesis
 * class of disease
 * pancreas disease agenesis pancreatic agenesis
 * pancreas disease that is characterized by the failure of the pancreas to develop prior to birth
 * DOID:0050877
 * partial retinal vein occlusion
 * class of disease
 * retinal vein occlusion
 * Human disease
 * DOID:1726
 * partial sensory epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3330
 * C10.228.140.490.360.275
 * partial third-nerve palsy
 * class of disease
 * paralytic squint oculomotor nerve paralysis
 * Human disease
 * DOID:10864
 * patellar tendinitis
 * class of disease
 * tendinitis knee disorder knee extensor tendonitis
 * Human disease
 * DOID:10471
 * Patellar tendinitis
 * patent blue V allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger patent blue V
 * DOID:0040080
 * paternal uniparental disomy of chromosome 14
 * class of disease
 * uniparental disomy of paternal origin uniparental disomy 14 syndrome
 * human disease
 * DOID:0111712
 * pathologic nystagmus
 * class of disease
 * nystagmus ocular motility disease abnormal eye movements
 * Human disease
 * DOID:9650
 * C10.292.562.675 C11.590.400
 * patterned macular dystrophy 1
 * class of disease
 * patterned macular dystrophy
 * human disease
 * DOID:0060866
 * patulous eustachian tube
 * class of disease physiological condition
 * eustachian tube disease
 * eustachian tube disorder
 * DOID:12358
 * peach allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus persica plant fruit food product.
 * DOID:0060510
 * peanut allergy
 * class of disease
 * tree nut allergy legume allergy vegetable allergy
 * type of food allergy caused by peanuts
 * DOID:4378
 * C20.543.480.370.572.750
 * Nut warning 1.jpg
 * pediatric CNS choriocarcinoma
 * class of disease
 * malignant childhood germ cell neoplasm central nervous system choriocarcinoma rare childhood malignant neoplasm choriocarcinoma
 * Human disease
 * DOID:6639
 * pediatric CNS embryonal cell carcinoma
 * class of disease
 * central nervous system childhood germ cell tumor central nervous system embryonal carcinoma rare childhood malignant neoplasm malignant childhood germ cell neoplasm brain cancer
 * Human disease
 * DOID:7231
 * pediatric angiosarcoma
 * class of disease
 * angiosarcoma rare childhood malignant neoplasm
 * angiosarcoma that affects children
 * DOID:4505
 * pediatric cerebral ependymoblastoma
 * class of disease
 * ependymoblastoma
 * Human disease
 * DOID:7841
 * pediatric ependymoma
 * class of disease
 * ependymoma childhood cancer ependymal tumor childhood neoplasm
 * human disease
 * DOID:5509
 * pediatric epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7095
 * pediatric fibrosarcoma
 * class of disease
 * fibrosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3520
 * pediatric germ cell tumor
 * class of disease
 * germ cell tumor childhood neoplasm
 * Human disease
 * DOID:6053
 * pediatric hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma childhood cancer of liver
 * Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age
 * DOID:0070322
 * pediatric infratentorial ependymoblastoma
 * class of disease
 * childhood infratentorial neoplasm ependymoblastoma infratentorial cancer childhood central nervous system primitive neuroectodermal neoplasm rare childhood malignant neoplasm
 * Human disease
 * DOID:7522
 * pediatric infratentorial ependymoma
 * class of disease
 * infratentorial cancer pediatric ependymoma brain ependymoma childhood infratentorial neoplasm childhood cancer
 * Human disease
 * DOID:7501
 * pediatric leptomeningeal melanoma
 * class of disease
 * meningeal melanoma
 * Human disease
 * DOID:6089
 * pediatric liposarcoma
 * class of disease
 * liposarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5695
 * pediatric low-grade glioma
 * class of disease
 * low grade glioma
 * human disease
 * DOID:0080830
 * pediatric lymphoma
 * class of disease
 * lymphoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5823
 * pediatric meningioma
 * class of disease
 * meningioma pediatric central nervous system tumor
 * Human disease
 * DOID:4593
 * pediatric mesenchymal chondrosarcoma
 * class of disease
 * mesenchymal chondrosarcoma childhood cancer
 * Human disease
 * DOID:4546
 * pediatric myxoid chondrosarcoma
 * class of disease
 * myxoid chondrosarcoma childhood cancer
 * Human disease
 * DOID:6494
 * pediatric osteosarcoma
 * class of disease
 * osteosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3361
 * pediatric ovarian dysgerminoma
 * class of disease
 * pediatric ovarian germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm dysgerminoma of ovary
 * dysgerminoma of ovary that occurs in children
 * DOID:7340
 * pediatric ovarian germ cell tumor
 * class of disease
 * ovarian germ cell neoplasm pediatric germ cell tumor
 * Human disease
 * DOID:6084
 * pediatric supratentorial ependymoma
 * class of disease
 * supratentorial cancer pediatric ependymoma brain ependymoma
 * Human disease
 * DOID:7502
 * pediatric testicular germ cell tumor
 * class of disease
 * testicular germ cell tumor pediatric germ cell tumor
 * Human disease
 * DOID:6082
 * peliosis hepatis
 * class of disease
 * hepatic vascular disease
 * Human disease
 * DOID:914
 * C06.552.802
 * Peliosis hepatis
 * pellagra
 * class of disease
 * nutritional deficiency disease other acquired skin disease skin disease disease
 * Human disease
 * DOID:8457
 * C18.654.521.500.133.699.529
 * Pellagra
 * Pellagra NIH.jpg
 * pelvic inflammatory diseases
 * class of disease
 * female reproductive system disease adnexal disease infectious disease disease
 * infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis
 * DOID:1003
 * C01.635.500 C12.050.351.500.056.750 C12.100.250.056.750
 * Pelvic inflammatory disease
 * Blausen 0732 PID-Sites.png
 * pelvic lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3927
 * pelvic muscle wasting
 * class of disease
 * pelvic organ prolapse pelvic floor dysfunction
 * Human disease
 * DOID:11629
 * pelvic organ prolapse
 * class of disease
 * female reproductive system disease prolapse
 * pelvic organs protruding from the opening of the vagina
 * DOID:1284
 * C23.300.842.624
 * Female genital prolapse
 * Hippocrates treatment for prolapse.png
 * pelvic varices
 * class of disease
 * varicose veins
 * Human disease
 * DOID:9742
 * pemphigoid
 * class of disease
 * autoimmune skin disease bullous skin disease
 * human disease
 * DOID:0080841
 * penicillin drug reaction
 * class of disease
 * adverse drug reaction beta-lactam allergy Side effects of penicillin
 * beta-lactam allergy triggered by penicillin
 * DOID:0060520
 * penicilliosis
 * class of disease
 * opportunistic mycosis disease
 * Human disease
 * DOID:0050288
 * penile cancer
 * class of disease
 * penile neoplasm male reproductive organ cancer penile disease disease
 * cancer of the penis
 * DOID:11615
 * Penile cancer
 * Penile cancer 2.jpg
 * penile disease
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:1529
 * C12.294.494
 * penile neoplasm
 * class of disease
 * male reproductive system neoplasm penile disease male reproductive organ benign neoplasm
 * human disease
 * DOID:11624
 * C04.588.945.440.715 C12.294.260.500 C12.294.494.591 C12.758.409.500
 * Penile neoplasms
 * penile urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8223
 * penis Paget's disease
 * class of disease
 * penis carcinoma extramammary Paget's disease adenocarcinoma of penis genetic urogenital tumor
 * Human disease
 * DOID:3448
 * Penile Paget's disease
 * penis basal cell carcinoma
 * class of disease
 * penis carcinoma basal-cell carcinoma rare skin disease
 * human disease
 * DOID:4277
 * penis basaloid carcinoma
 * class of disease
 * penis squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7047
 * penis carcinoma
 * class of disease
 * penile cancer carcinoma
 * penile cancer that is located in the skin or tissues of the penis
 * DOID:3449
 * penis carcinoma in situ
 * class of disease
 * in situ carcinoma penile disease penis squamous cell carcinoma carcinoma in situ of male genital organs
 * Human disease
 * DOID:8872
 * penis mixed squamous cell carcinoma
 * class of disease
 * penis squamous cell carcinoma
 * Human disease
 * DOID:8009
 * penis non-invasive verrucous carcinoma
 * class of disease
 * penis verrucous carcinoma penis carcinoma in situ cervical verrucous carcinoma
 * Human disease
 * DOID:5907
 * penis papillary carcinoma
 * class of disease
 * penis squamous cell carcinoma papillary squamous carcinoma
 * Human disease
 * DOID:8013
 * penis sarcoma
 * class of disease
 * penile cancer sarcoma
 * sarcoma and malignant neoplasm of penis that is located in the penis
 * DOID:11838
 * penis squamous cell carcinoma
 * class of disease
 * penis carcinoma squamous cell carcinoma
 * penis carcinoma that has material basis in squamous cells
 * DOID:5518
 * Squamous-cell carcinoma of the penis
 * penis verrucous carcinoma
 * class of disease
 * penis squamous cell carcinoma verrucous carcinoma penis papillary carcinoma
 * Human disease
 * DOID:5908
 * peptic esophagitis
 * class of disease
 * peptic ulcer disease esophagitis gastroesophageal reflux disease
 * human disease
 * DOID:13976
 * C06.405.117.620.420 C06.405.205.663.420 C06.405.469.275.800.523 C06.405.748.586.524
 * peptic ulcer disease
 * class of disease
 * gastrointestinal system disease duodenal disease disease
 * ulcer of an area of the gastrointestinal tract
 * DOID:750
 * C06.405.469.275.800 C06.405.748.586
 * Peptic ulcers
 * Benign gastric ulcer 1.jpg
 * perforated corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10445
 * perforated ulcer
 * class of disease
 * peptic ulcer disease gastric perforation
 * medical condition of the gastrointestinal tract wall
 * DOID:752
 * C06.405.469.275.800.698 C06.405.748.586.698
 * DU 2.jpg
 * perforation of bile duct
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:13409
 * periampullary adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma
 * Human disease
 * DOID:8110
 * periampullary adenoma
 * class of disease
 * ampulla of Vater neoplasm adenoma
 * Human disease
 * DOID:0050849
 * perianal gland tumor
 * class of disease
 * cancer in dogs anus neoplasm
 * dog disease
 * DOID:4550
 * C04.588.083 C04.588.274.476.411.307.790.040.040 C06.301.371.411.307.790.040.040 C06.405.249.411.307.790.040.040 C06.405.469.491.307.790.040.040 C06.405.469.860.101.163.083 C06.405.469.860.180.500.040.040 C22.073
 * perianal hematoma
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9745
 * Perianal hematoma
 * perianal skin Paget's disease
 * class of disease
 * anal margin carcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:7708
 * periapical abscess
 * class of disease
 * periapical periodontitis dental abscess
 * localized collection of pus associated with a tooth
 * DOID:2562
 * C01.539.830.025.650 C07.320.830.700.700 C07.465.714.306.700.700 C07.465.714.533.487.700
 * periapical periodontitis
 * class of disease
 * inflammation periodontitis dental pulp disease periapical disease tooth pathology
 * Human disease
 * DOID:823
 * C07.320.830.700 C07.465.714.306.700 C07.465.714.533.487
 * pericardial effusion
 * class of disease symptom or sign
 * pericardium disease cardiovascular system symptom disease
 * pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
 * DOID:118
 * C14.280.695
 * Pericardial effusion
 * pericardial mesothelioma
 * class of disease
 * pericardium cancer mesothelioma
 * Human disease
 * DOID:6201
 * pericarditis
 * class of disease
 * pericardium disease inflammation inflammatory disease heart disease disease
 * pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
 * DOID:1787
 * C14.280.720
 * Pericarditis
 * Pericarditis10.JPG
 * pericardium cancer
 * class of disease
 * heart cancer neoplasm of pericardium pericardium disease
 * Human disease
 * DOID:116
 * pericardium leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of pericardium pericardium disease cardiovascular organ benign neoplasm
 * Human disease
 * DOID:5137
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * Gastritis erosiva.2278.jpg
 * gastroduodenal Crohn's disease
 * class of disease
 * Crohn's disease
 * inflammatory bowel disease characterized by inflammation located in stomach and located in duodenum, has symptom nausea, has symptom vomiting, has symptom weight loss and has symptom loss of appetite
 * DOID:0060191
 * gastroduodenitis
 * class of disease
 * peptic ulcer disease hemorrhagic duodenitis gastritis disease
 * Human disease
 * DOID:8644
 * gastroenteritis
 * class of disease symptom or sign
 * gastrointestinal system disease digestive sign disease
 * medical condition characterized by inflammation of the stomach and/or small intestine
 * DOID:2326
 * C06.405.205
 * Gastroenteritis
 * Gastroenteritis viruses.jpg
 * gastroesophageal adenocarcinoma
 * class of disease
 * adenocarcinoma gastroesophageal cancer
 * gastroesophageal cancer that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue
 * DOID:0080375
 * gastroesophageal cancer
 * class of disease
 * gastrointestinal system cancer
 * gastrointestinal system cancer that is located in the proximal esophagus and the distal stomach
 * DOID:0080374
 * gastroesophageal junction adenocarcinoma
 * class of disease
 * gastrointestinal carcinoma gastroesophageal adenocarcinoma
 * Human disease
 * DOID:4944
 * gastroesophageal reflux disease
 * class of disease
 * genetic disease stomach disease esophagitis gastrointestinal system disease esophageal disease
 * chronic disease caused by stomach acid coming up from the stomach into the esophagus
 * DOID:8534
 * C06.405.117.119.500.484
 * Gastroesophageal reflux disease
 * Peptic stricture.png
 * gastrointestinal adenoma
 * class of disease
 * gastrointestinal system cancer adenoma gastrointestinal system benign neoplasm
 * Human disease
 * DOID:4147
 * gastrointestinal allergy
 * class of disease
 * allergy
 * hypersensitivity reaction type I disease located in the gastrointestinal tract
 * DOID:0060502
 * gastrointestinal anthrax
 * class of disease
 * anthrax gastrointestinal system disease
 * human disease
 * DOID:13386
 * gastrointestinal carcinoma
 * class of disease
 * gastrointestinal system cancer carcinoma
 * gastrointestinal system cancer that has material basis in epithelial cells
 * DOID:0050922
 * gastrointestinal lymphoma
 * class of disease
 * gastrointestinal system cancer gastrointestinal system disease non-Hodgkin lymphoma lymphoma
 * Human disease
 * DOID:903
 * gastrointestinal neuroendocrine benign tumor
 * class of disease
 * gastrointestinal system benign neoplasm gastrointestinal system disease gastroenteropancreatic neuroendocrine neoplasm
 * Human disease
 * DOID:4148
 * gastrointestinal neuroendocrine tumor
 * class of disease
 * gastrointestinal neoplasm neuroendocrine tumor gastrointestinal system cancer
 * gastrointestinal system cancer that has material basis in neuroendocrine cells
 * DOID:0050626
 * gastrointestinal stromal tumor
 * class of disease
 * Stromal tumor rare genetic intestinal disease inherited digestive tract tumor mesenchymal tumor of small intestine gastrointestinal system cancer
 * human disease
 * DOID:9253
 * C04.557.450.565.370 C06.301.371.308 C06.405.249.308
 * Gastrointestinal stromal tumors
 * GIST 2.jpg
 * gastrointestinal system benign neoplasm
 * class of disease
 * organ system benign neoplasm gastrointestinal neoplasm gastrointestinal system disease
 * organ system benign neoplasm located in gastrointestinal tract organs
 * DOID:0050624
 * Benign neoplasms of gastrointestinal tract
 * gastrointestinal system cancer
 * class of disease
 * digestive system cancer gastrointestinal neoplasm organ system cancer gastrointestinal system disease
 * organ system cancer located in gastrointestinal tract that is manifested in organs of the gastrointestinal system
 * DOID:3119
 * Gastrointestinal cancers
 * gastrointestinal system disease
 * class of disease
 * disease of anatomical entity disease
 * disease involving the gastrointestinal tract
 * DOID:77
 * C06
 * Diseases and disorders of the digestive system
 * gastrointestinal tularemia
 * class of disease
 * tularemia gastrointestinal system disease
 * tularemia that results in formation of ulcerative lesions located in gastrointestinal tract
 * DOID:14239
 * gastrojejunal ulcer
 * class of disease
 * peptic ulcer disease
 * Human disease
 * DOID:10927
 * gastroparesis
 * class of disease
 * functional gastric disease disease
 * Human disease
 * DOID:11914
 * C06.405.748.543 C23.888.592.636.263
 * Gastroparesis
 * GastroparesisXray.jpg
 * geleophysic dysplasia 1
 * class of disease
 * geleophysic dysplasia autosomal recessive disease
 * human disease
 * DOID:0111725
 * geleophysic dysplasia 3
 * class of disease
 * geleophysic dysplasia autosomal dominant disease
 * human disease
 * DOID:0111727
 * gemistocytic astrocytoma
 * class of disease
 * astrocytoma
 * human disease
 * DOID:7005
 * Histopathology of gemistocytic astrocytoma.jpg
 * gender dysphoria
 * class of disease
 * mental disorder dysphoria disease
 * mental distress resulting from mismatch between gender identity and biological gender assigned at birth
 * DOID:1234
 * F03.835.550
 * gene duplication disease
 * class of disease
 * monogenic disease
 * human disease
 * DOID:0080712
 * generalized anxiety disorder
 * class of disease
 * anxiety disorder disease
 * anxiety disorder that is characterized by long-lasting anxiety that is not focused on any one object or situation
 * DOID:14320
 * Generalized anxiety disorder
 * generalized atherosclerosis
 * class of disease
 * atherosclerosis
 * Human disease
 * DOID:2347
 * generalized dystonia
 * class of disease
 * dystonia
 * human disease
 * DOID:0050835
 * C10.228.140.079.357 C10.228.662.300.200 C10.574.500.393 C16.320.400.330
 * generalized epidermolysis bullosa simplex
 * class of disease
 * epidermolysis bullosa simplex basal epidermolysis bullosa simplex autosomal dominant disease
 * epidermolysis bullosa simplex that is characterized by widespread blisters that appear at birth or in early infancy
 * DOID:0080511
 * generalized epilepsy
 * class of disease
 * epilepsy seizure
 * epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from independent foci or epileptic circuits that involve the whole brain
 * DOID:1827
 * C10.228.140.490.375
 * generalized epilepsy with febrile seizures plus 1
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111302
 * generalized epilepsy with febrile seizures plus 10
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111296
 * generalized epilepsy with febrile seizures plus 2
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111294
 * generalized epilepsy with febrile seizures plus 4
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111293
 * generalized epilepsy with febrile seizures plus 6
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111300
 * generalized epilepsy with febrile seizures plus 7
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111295
 * generalized epilepsy with febrile seizures plus 8
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111299
 * generalized epilepsy with febrile seizures plus 9
 * class of disease
 * generalized epilepsy with febrile seizures plus
 * human disease
 * DOID:0111301
 * genetic disease
 * class of disease
 * hereditary disorder disease
 * health problem caused by one or more abnormalities in the genome
 * DOID:630 DOID:0050325
 * C16.320
 * Genetic diseases and disorders
 * geniculate ganglionitis
 * class of disease
 * facial nerve disease
 * Human disease
 * DOID:14075
 * geniculate herpes zoster
 * class of disease
 * herpes zoster poliomyelitis facial nerve disease
 * disorder that is caused by the reactivation of varicella zoster virus in the geniculate ganglion, a nerve cell bundle of the facial nerve
 * DOID:9210
 * C01.925.256.466.930.750.733 C07.465.299.750 C09.218.513 C10.292.319.750
 * Ramsay Hunt syndrome type II
 * genital leiomyoma
 * class of disease
 * reproductive organ benign neoplasm leiomyoma cutis
 * human disease
 * DOID:5147
 * geographic tongue
 * class of disease symptom or sign
 * inflammation tongue disease smooth tongue disease
 * atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface
 * DOID:1455
 * C07.465.910.363.447
 * Geographic tongue
 * germ cell and embryonal cancer
 * class of disease
 * germ cell cancer sarcoma
 * germ cell cancer that is derives from a mixture of germs cells and embryonal cells
 * DOID:3095
 * germ cell benign neoplasm
 * class of disease
 * benign neoplasms by histologic type germ cell tumor
 * human disease
 * DOID:0080601
 * germ cell cancer
 * class of disease
 * cell type cancer germ cell tumor
 * A cell type cancer that has_material_basis_in abnormally proliferating cells derived_from germ cells.
 * DOID:2994
 * Germ cell cancers
 * germinoma
 * class of disease
 * germ cell cancer disease
 * germ cell cancer that lacks histologic differentiation, usually a brain tumor
 * DOID:3304
 * C04.557.465.330
 * Germinoma
 * gestational choriocarcinoma
 * class of disease
 * choriocarcinoma extragonadal non-dysgerminomatous germ cell tumor extragonadal germ cell cancer gestational trophoblastic disease
 * Human disease
 * DOID:2025
 * gestational diabetes
 * class of disease
 * diabetes complication of pregnancy, childbirth and the puerperium diabetes mellitus and pregnancy disease
 * condition in which a woman without diabetes develops high blood sugar levels during pregnancy
 * DOID:11714 DOID:1550
 * C12.050.703.170 C18.452.394.750.448 C19.246.200
 * Gestational diabetes
 * Blue circle for diabetes.svg
 * gestational ovarian choriocarcinoma
 * class of disease
 * choriocarcinoma of ovary malignant non-dysgerminomatous germ cell tumor of ovary ovarian cancer gestational choriocarcinoma
 * Human disease
 * DOID:7591
 * gestational uterine corpus choriocarcinoma
 * class of disease
 * gestational choriocarcinoma uterine corpus choriocarcinoma
 * Human disease
 * DOID:8187
 * giant axonal neuropathy
 * class of disease
 * axonal neuropathy genetic disease autosomal recessive disease
 * human disease
 * DOID:0090068
 * C10.500.300.490 C10.574.500.495.490 C10.668.829.325 C10.668.829.800.300.490 C16.131.666.300.490 C16.320.400.375.490
 * giant cell glioblastoma
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by a prevalence of bizarre, multinucleated giant cells
 * DOID:3074
 * giant cell reparative granuloma
 * class of disease
 * giant-cell tumor of bone
 * Human disease
 * DOID:1866
 * C05.500.368 C07.320.391 C07.465.714.258.557 C23.550.382.468
 * giant cell tumor
 * class of disease
 * connective tissue neoplasm bone benign neoplasm
 * Human disease
 * DOID:200
 * C04.557.450.565.380
 * Giant cell tumors
 * giant hemangioma
 * class of disease
 * cavernous hemangioma
 * Human disease
 * DOID:5774
 * giant papillary conjunctivitis
 * class of disease
 * blepharoconjunctivitis papillary conjunctivitis allergic conjunctivitis
 * Human disease
 * DOID:2457
 * giant-cell carcinoma of the lung
 * class of disease
 * large-cell lung carcinoma Sarcomatoid carcinoma of the lung malignant giant cell tumor
 * lung carcinoma that is located in large undifferentiated cells
 * DOID:5583
 * C04.557.470.200.220
 * Giant cell carcinoma - Case 284 (13107156794).jpg
 * giant-cell tumor of bone
 * class of disease
 * bone neoplasm giant cell tumor disease
 * giant cell tumor and bone cancer and bone tissue neoplasm that results in the presence of multinucleated giant cells (osteoclast-like cell)
 * DOID:4305
 * C04.557.450.565.380.380 C04.557.450.565.575.420
 * Giant-cell tumor of bone
 * Giant cell tumour of bone - high mag.jpg
 * gingival disease
 * class of disease
 * periodontal disease
 * human disease
 * DOID:1483
 * C07.465.714.258
 * gingival fibromatosis 5
 * class of disease
 * gingival fibromatosis autosomal dominant disease
 * human disease
 * DOID:0080280
 * gingival hypertrophy
 * class of disease
 * gingival overgrowth
 * Human disease
 * DOID:5338
 * C07.465.714.258.428.260
 * gingival overgrowth
 * class of disease
 * gingival disease
 * Human disease
 * DOID:3086
 * C07.465.714.258.428
 * Gingival enlargement
 * gingival recession
 * class of disease
 * gingival disease periodontal atrophy
 * human disease
 * DOID:1134
 * C07.465.714.258.447 C07.465.714.354.625
 * Gingival recession
 * gingivitis
 * class of disease symptom or sign
 * symptom gingival disease periodontitis disease
 * inflammation of the gums
 * DOID:3087
 * C07.465.714.258.480
 * Gingivitis
 * Gingivitis (crop).jpg
 * glandular cystitis
 * class of disease
 * chronic cystitis
 * A reactive inflammatory disorder affecting the bladder. It is characterized by the development of small cysts in the bladder wall. The cysts are lined by metaplastic glandular cells.
 * DOID:2392
 * Cystitis glandularis
 * glandular pattern ovarian yolk sac tumor
 * class of disease
 * ovarian endodermal sinus tumor
 * Human disease
 * DOID:6511
 * glandular tularemia
 * class of disease
 * tularemia
 * tularemia that results in swelling of regional lymph glands
 * DOID:0050382
 * glandular-alveolar pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:7930
 * glans penis cancer
 * class of disease
 * penile cancer
 * Human disease
 * DOID:11839
 * glassy cell variant cervical adenosquamous carcinoma
 * class of disease
 * cervical adenosquamous carcinoma
 * cervical adenosquamous carcinoma that is a rare form and is composed of cells with a glass-like cytoplasm
 * DOID:8361
 * glaucoma
 * class of disease
 * eye disease disease
 * eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function
 * DOID:1686
 * C11.525.381
 * Glaucoma
 * Acute Angle Closure-glaucoma.jpg
 * glaucomatous atrophy of optic disc
 * class of disease
 * optic atrophy eye degenerative disease
 * human disease
 * DOID:10337
 * glioblastoma
 * class of disease
 * astrocytoma disease
 * human disease
 * DOID:3068
 * C04.557.465.625.600.380.080.335 C04.557.470.670.380.080.335 C04.557.580.625.600.380.080.335
 * Glioblastoma
 * Glioblastoma (1).jpg
 * glioblastoma classical subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by abnormally high levels of epidermal growth factor receptor and the absence of p53 mutations
 * DOID:0050803
 * glioblastoma mesenchymal subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by the most frequent number of mutation of the Neurofibromin 1 gene
 * DOID:0050805
 * glioblastoma neural subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by the expression of several gene types that are also typical of the brain&#39;s normal, noncancerous nerve cells, or neurons
 * DOID:0050806
 * glioblastoma proneural subtype
 * class of disease
 * glioblastoma
 * glioblastoma multiforme that is characterized by IDH1 and p53 mutations and Platelet Derived Growth Factor A amplification
 * DOID:0050804
 * glioma
 * class of disease
 * cell type cancer brain tumor spinal disease bone cancer brain cancer disease
 * type of tumor that starts in the brain or spine
 * DOID:3070
 * C04.557.465.625.600.380 C04.557.470.670.380 C04.557.580.625.600.380
 * Gliomas
 * Glioma.gif
 * gliomatosis cerebri
 * class of disease
 * brain cancer
 * rare primary brain tumor
 * DOID:6128
 * Gliomatosis cerebri
 * Gliomatosis cerebri.jpg
 * gliosarcoma
 * class of disease
 * glioblastoma
 * Human disease
 * DOID:3071
 * C04.557.465.625.600.380.400 C04.557.470.670.380.400 C04.557.580.625.600.380.400
 * Gliosarcoma
 * globe disease
 * class of disease
 * eye disease
 * Human disease
 * DOID:1242
 * globoszoospermia
 * class of disease
 * Teratospermia male infertility autosomal recessive disease spermatogenic failure
 * male infertility characterized by round-headed spermatozoa lacking an acrosome
 * DOID:0111156
 * Globoszoospermia
 * Globozoospermia.png
 * glomangioma
 * class of disease
 * benign perivascular tumor glomus tumor
 * Human disease
 * DOID:2436
 * glomangiomatosis
 * class of disease
 * benign perivascular tumor glomus tumor
 * Human disease
 * DOID:6906
 * glomangiomyoma
 * class of disease
 * benign perivascular tumor glomus tumor
 * human disease
 * DOID:8020
 * glomangiosarcoma
 * class of disease
 * glomus tumor
 * Human disease
 * DOID:5233
 * glomeruloid hemangioma
 * class of disease
 * hemangioma
 * Human disease
 * DOID:486
 * glomerulonephritis
 * class of disease symptom or sign
 * nephritis glomerulopathy disease
 * nephritis that causes inflammation of the glomeruli located in kidney
 * DOID:2921
 * C12.777.419.570.363 C13.351.968.419.570.363
 * Glomerulonephritis
 * Crescentic glomerulonephritis HE stain.JPEG
 * glomerulosclerosis
 * class of disease
 * glomerulonephritis
 * glomerulonephritis that is characterized by hardening of the glomerulus in the kidney
 * DOID:0050851
 * Glomerulosclerosis
 * glossitis
 * class of disease symptom or sign
 * tongue disease inflammatory disease disease
 * soreness of the tongue, or more usually inflammation with depapillation of the dorsal surface of the tongue
 * DOID:1456
 * C07.465.910.363
 * Glossitis
 * Scharlach.JPG
 * glossopharyngeal motor neuropathy
 * class of disease
 * motor neuritis glossopharyngeal nerve disease
 * Human disease
 * DOID:7558
 * glossopharyngeal nerve disease
 * class of disease
 * cranial nerve disease
 * Human disease
 * DOID:3418
 * C10.292.450
 * glossopharyngeal nerve paralysis
 * class of disease
 * glossopharyngeal nerve disease cranial nerve palsy
 * Human disease
 * DOID:3816
 * glossopharyngeal neuralgia
 * class of disease
 * glossopharyngeal nerve disease neuralgia cranial neuralgia
 * Human disease
 * DOID:14423
 * glottis cancer
 * class of disease
 * laryngeal cancer glottis neoplasm
 * Human disease
 * DOID:2595
 * glottis carcinoma
 * class of disease
 * glottis cancer carcinoma
 * Human disease
 * DOID:2599
 * glottis neoplasm
 * class of disease
 * laryngeal neoplasm
 * Human disease
 * DOID:2597
 * glucocorticoid deficiency 1
 * class of disease
 * familial glucocorticoid deficiency autosomal recessive disease
 * human disease
 * DOID:0080621
 * glucocorticoid-induced osteoporosis
 * class of disease
 * corticosteroid-induced osteoporosis osteoporosis
 * Human disease
 * DOID:0060343
 * glucose intolerance
 * class of disease
 * hyperglycemia disease
 * pre-diabetic state of hyperglycemia that is associated with insulin resistance and increased risk of cardiovascular pathology. IGT may precede type 2 diabetes mellitus by many years
 * DOID:10603
 * C18.452.394.952.500
 * glucose metabolism disease
 * class of disease
 * carbohydrate metabolism disease metabolic disease
 * metabolic disorder characterized by abnormal blood glucose levels
 * DOID:4194
 * C18.452.394
 * Glucose metabolism disorders
 * glucose-6-phosphate dehydrogenase deficiency
 * class of disease
 * carbohydrate metabolic disorder disease
 * carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH)
 * DOID:2862
 * C15.378.071.141.150.480 C16.320.070.480 C16.320.565.202.402 C18.452.648.202.402
 * Glucose-6-phosphate dehydrogenase deficiency
 * G6PD - 3D structure - PDB1qki.png
 * glutathionuria
 * class of disease
 * Congenital disorders of amino acid metabolism inborn disorder of the gamma-glutamyl cycle amino acid metabolic disorder autosomal recessive disease
 * Gamma-glutamyl transpeptidase deficiency is characterized by increased glutathione concentration in the plasma and urine
 * DOID:0111257
 * gluten allergy
 * class of disease
 * food allergy gluten-related disorder
 * allergy involving gluten
 * DOID:0060057
 * glycogen metabolism disorder
 * class of disease
 * carbohydrate metabolic disorder
 * carbohydrate metabolism disorder that is characterized by abnormal accumulation or depletion of liver glycogen
 * DOID:0050728
 * glycogen storage disease
 * class of disease
 * glycogen metabolism disorder overload disease carbohydrate metabolic disorder disease
 * glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types
 * DOID:2747
 * C16.320.565.202.449 C18.452.648.202.449
 * Glycogen storage disease
 * Glycogen storage disorder (PAS with diastase).jpg
 * glycogen storage disease IX
 * class of disease
 * glycogen storage disease
 * glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity
 * DOID:0050594
 * Glycogen storage disease type IX
 * glycogen-rich clear cell breast carcinoma
 * class of disease
 * breast adenocarcinoma clear cell carcinoma
 * Human disease
 * DOID:5310
 * goat milk allergy
 * class of disease
 * milk allergy
 * milk allergy triggered by Capra hircus milk
 * DOID:0060522
 * goiter
 * class of disease
 * thyroid gland disease disease
 * swelling of the thyroid gland
 * DOID:12176
 * C19.874.283
 * Goiters
 * Kone med stor struma.jpg
 * gonadal disease
 * class of disease
 * endocrine system disease
 * endocrine system disease that is located in the gonads
 * DOID:2277
 * C19.391
 * Diseases and disorders of gonads
 * gonadal dysgenesis
 * class of disease
 * hypogonadism sex differentiation disease disease
 * congenital disorder of the reproductive system
 * DOID:14447
 * C12.706.316.309 C13.351.875.253.309 C16.131.939.316.309 C19.391.119.309
 * gonadoblastoma
 * class of disease
 * benign neoplasms by histologic type
 * cell type benign neoplasm that is composed of a mixture of gonadal elements
 * DOID:3301
 * C04.557.465.420 C04.557.475.395 C12.706.316.096.687.500 C12.706.316.309.388.500 C13.351.875.253.096.687.500 C13.351.875.253.309.388.500 C16.131.939.316.096.687.500 C16.131.939.316.309.388.500 C19.391.119.096.687.500 C19.391.119.309.388.500
 * Gonadoblastoma
 * gonococcal bursitis
 * class of disease
 * bursitis gonococcal infectious diseases
 * Human disease
 * DOID:13453
 * gonococcal seminal vesiculitis
 * class of disease
 * vesiculitis gonorrhea
 * human disease
 * DOID:10400
 * gonococcal spondylitis
 * class of disease
 * spondylitis gonorrhea
 * Human disease
 * DOID:13127
 * gonococcal synovitis
 * class of disease
 * synovitis gonococcal infectious diseases
 * Human disease
 * DOID:13454
 * gout
 * class of disease symptom or sign
 * arthritis genetic disease crystal arthropathy metabolic disease disease
 * medical condition that results in recurrent pain and swelling of joints
 * DOID:13189
 * C05.550.114.423 C05.550.354.500 C05.799.414 C16.320.565.798.368 C18.452.648.798.368
 * Gout
 * Gout2010.JPG
 * granular cell carcinoma
 * class of disease
 * carcinoma
 * carcinoma that derives from epithelial cells, with polygonal accumulation of secondary lysosomes in the cytoplasm
 * DOID:4903
 * granular cell leiomyosarcoma
 * class of disease
 * leiomyosarcoma rare nervous system tumor malignant granular cell myoblastoma
 * Human disease
 * DOID:5258
 * granular cell tumor
 * class of disease
 * skin benign neoplasm
 * Human disease
 * DOID:2411
 * C04.557.450.590.350
 * Granular cell tumor
 * Granular cell tumor Case 174 (5600864519).jpg
 * granuloma annulare
 * class of disease
 * dermatitis necrobiotic disorders
 * Human disease
 * DOID:3777
 * C17.300.200.495.380 C17.800.550.380 C23.550.382.375
 * Granuloma annulare
 * Granuloma annulare.jpg
 * granulomatous amebic encephalitis
 * class of disease
 * Balamuthia infection acanthamoebiasis primary amebic meningoencephalitis encephalopathy
 * Human disease
 * DOID:0050246
 * Granulomatous amoebic encephalitis
 * granulomatous angiitis
 * class of disease
 * vasculitis central nervous system vasculitis
 * Human disease
 * DOID:2555
 * granulomatous dermatitis
 * class of disease
 * dermatitis
 * Human disease
 * DOID:4397
 * granulomatous endometritis
 * class of disease
 * endometritis chronic endometritis
 * Human disease
 * DOID:4561
 * granulomatous gastritis
 * class of disease
 * gastritis chronic gastritis
 * Human disease
 * DOID:4038
 * granulomatous hepatitis
 * class of disease
 * hepatitis hepatic granuloma
 * Human disease
 * DOID:2239
 * granulomatous myositis
 * class of disease
 * myositis
 * Human disease
 * DOID:3428
 * granulomatous orchitis
 * class of disease
 * testicular disease
 * Human disease
 * DOID:3089
 * granulosa cell tumour
 * class of disease
 * ovarian cancer sex cord-gonadal stromal tumor
 * Human disease
 * DOID:2999
 * C04.557.475.750.656 C04.588.322.455.398 C13.351.500.056.630.705.398 C13.351.937.418.685.398 C19.344.410.398 C19.391.630.705.398
 * Granulosa cell tumors
 * gray zone lymphoma
 * class of disease
 * lymphoma
 * lymphoma that is characterized by having cellular features of both classic Hodgkin&#39;s lymphomas and large B-cell Lymphomas
 * DOID:5822
 * green color blindness
 * class of disease
 * dichromatopsia deuteranopia
 * human disease
 * DOID:13909
 * green mud crab allergy
 * class of disease
 * crustacean allergy
 * crustacean allergy triggered by Scylla paramamosain
 * DOID:0060526
 * growth hormone insensitivity syndrome with immune dysregulation 2
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0080837
 * growth hormone secreting pituitary adenoma 2
 * class of disease
 * growth hormone secreting pituitary adenoma
 * human disease
 * DOID:0112007
 * gynatresia
 * class of disease
 * female reproductive system disease atresia
 * Human disease
 * DOID:429
 * C13.351.500.320
 * gynecomastia
 * class of disease
 * sex differentiation disease
 * human disorder, which causes the appearance of breasts in males
 * DOID:12698
 * C17.800.090.875
 * Gynecomastia
 * gyrate atrophy of the choroid
 * class of disease
 * disease choroid disease central gyrate choroidal dystrophy
 * Human disease
 * DOID:1415
 * C11.270.468 C11.941.160.578 C16.320.290.468
 * haemophilus meningitis
 * class of disease
 * bacterial meningitis Haemophilus influenzae infectious disease
 * bacterial meningitis that has material basis in Haemophilus influenzae infection
 * DOID:0080179
 * C01.150.252.223.500.425 C01.150.252.400.700.433.615 C10.228.228.180.500.425 C10.586.625.280.393 C01.207.180.500.425
 * hair diseases
 * class of disease
 * integumentary system disease
 * integumentary system disease that is located in hair
 * DOID:421
 * C17.800.329
 * hair follicle neoplasm
 * class of disease
 * skin benign neoplasm hair diseases
 * skin tumor derived from the hair matrix
 * DOID:5375
 * hairy cell leukemia
 * class of disease
 * chronic lymphocytic leukemia B-cell leukemia disease
 * chronic lymphocytic leukemia that is characterized by over production of B cells (lymphocytes) by the bone marrow where the B cells appear hairy under a microscope
 * DOID:285
 * C04.557.337.415 C15.604.515.553 C20.683.515.517
 * Hairy cell leukemia
 * hairy tongue
 * class of disease
 * tongue disease disease
 * Human disease
 * DOID:13500
 * C07.465.910.791
 * Black hairy tongue
 * Black tongue.jpg
 * hallucinogen abuse
 * class of disease
 * substance abuse
 * substance abuse that involves the recurring use of hallucinogenic drugs despite negative consequences
 * DOID:12797
 * hallucinogen dependence
 * class of disease
 * substance dependence hallucinogen abuse
 * drug dependence that involves the continued use of hallucinogenic drugs despite problems related to use of the substance
 * DOID:9977
 * hand dermatosis
 * class of disease
 * skin disease
 * disease class
 * DOID:3158
 * C17.800.338
 * head and neck cancer
 * class of disease
 * organ system cancer head and neck neoplasms respiratory system cancer disease
 * organ system cancer in the head or neck region
 * DOID:11934 DOID:3680
 * Head and neck cancer
 * PET-CT scanning of lymph node metastases in cancer 2.jpg
 * head and neck carcinoma
 * class of disease
 * head and neck cancer carcinoma
 * human disease
 * DOID:1542
 * heart cancer
 * class of disease
 * cardiovascular cancer Primary tumors of the heart heart disease thoracic cancer
 * cardiovascular cancer located in the heart
 * DOID:117
 * Heart cancer
 * Myxoma.jpg
 * heart disease
 * class of disease
 * cardiovascular disease
 * cardiovascular system disease that involves the heart
 * DOID:114
 * C14.280
 * Diseases and disorders of the heart
 * heart fibrosarcoma
 * class of disease
 * heart sarcoma fibrosarcoma
 * Human disease
 * DOID:6033
 * heart leiomyosarcoma
 * class of disease
 * heart sarcoma
 * Human disease
 * DOID:5261
 * heart lipoma
 * class of disease
 * cardiovascular organ benign neoplasm Primary tumors of the heart heart disease benign neoplasm of heart lipoma
 * Human disease
 * DOID:6285
 * heart lymphoma
 * class of disease
 * heart cancer lymphoma
 * Human disease
 * DOID:6547
 * heart malignant hemangiopericytoma
 * class of disease
 * heart sarcoma hemangiopericytoma
 * heart sarcoma that is a soft tissue sarcoma located in the heart
 * DOID:6034
 * heart sarcoma
 * class of disease
 * heart cancer
 * sarcoma and malignant neoplasm of heart that is located in the heart
 * DOID:5262
 * heart septal defect
 * class of disease
 * congenital heart disease
 * Human disease
 * DOID:1681
 * C14.240.400.560 C14.280.400.560 C16.131.240.400.560
 * Heart septal defects
 * heart valve disease
 * class of disease
 * heart disease disease
 * disease in the valves of the heart
 * DOID:4079
 * C14.280.484
 * Diseases and disorders of the heart valves
 * heavy chain disease
 * class of disease
 * type IV hypersensitivity
 * hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains
 * DOID:0060125
 * C15.378.147.780.490 C15.604.515.435 C20.683.780.490
 * hemangioblastoma
 * class of disease
 * hemangioma rare nervous system tumor disease
 * tumor of the central nervous system that originates from the vascular system
 * DOID:5241
 * C04.557.645.375.380.370
 * Hemangioblastomas
 * Hemangioblastoma cerebellum.jpg
 * hemangioma
 * class of disease
 * angioma vascular neoplasm cardiovascular organ benign neoplasm benign neoplasms by histologic type vascular disease disease
 * cell type benign neoplasm that has physical basis in endothelial cells that line blood vessels
 * DOID:255
 * C04.557.645.375
 * Skin hemangioma
 * Capillary haemangioma.jpg
 * hemangioma of intra-abdominal structure
 * class of disease
 * hemangioma
 * Human disease
 * DOID:254
 * hemangioma of lung
 * class of disease
 * hemangioma lung benign neoplasm
 * human disease
 * DOID:490
 * hemangioma of orbit
 * class of disease
 * orbital disease hemangioma
 * Human disease
 * DOID:14459
 * hemangioma of peripheral nerve
 * class of disease
 * hemangioma peripheral nervous system benign neoplasm peripheral neuropathy
 * Human disease
 * DOID:482
 * hemangioma of spleen
 * class of disease
 * splenic disease hemangioma of intra-abdominal structure
 * Human disease
 * DOID:256
 * hemangioma of subcutaneous tissue
 * class of disease
 * skin hemangioma subcutaneous tissue disease vascular skin disease skin benign neoplasm hemangioma
 * Human disease
 * DOID:13081
 * hemangiopericytic tumor
 * class of disease
 * perivascular tumor
 * Human disease
 * DOID:3850
 * hemangiopericytoma
 * class of disease
 * connective tissue neoplasm hemangiopericytic tumor
 * soft tissue cancer that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries
 * DOID:264
 * C04.557.645.380
 * Haemangiopericytoma
 * hematocele of tunica vaginalis testis
 * class of disease symptom or sign
 * testicular disease hematocele
 * Human disease
 * DOID:12332
 * C12.294.287 C23.550.414.817
 * Hematocele
 * hematologic cancer
 * class of disease symptom or sign
 * organ system cancer hematopoietic system disease tumor of hematopoietic and lymphoid tissues
 * immune system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes
 * DOID:2531
 * Cancers of the lymph nodes and haematopoiesis
 * hematopoietic system disease
 * class of disease
 * symptom disease of anatomical entity
 * disorder which primarily affects the blood
 * DOID:74
 * C15.378
 * Diseases and disorders of the blood
 * hemidystonia
 * class of disease
 * multifocal dystonia
 * multifocal dystonia that involves the arm and leg on the same side of the body
 * DOID:0050846
 * hemiparesis
 * class of disease symptom or sign
 * paresis paralysis central nervous system disease disease
 * weakness of one side of the body
 * DOID:10969
 * hemochromatosis type 1
 * class of disease
 * HFE hereditary haemochromatosis genetic disease
 * hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22
 * DOID:0111029
 * hemochromatosis type 2
 * class of disease
 * iron overload HFE hereditary haemochromatosis
 * hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis
 * DOID:0111034
 * hemochromatosis type 2B
 * class of disease
 * hemochromatosis type 2 genetic disease
 * hemochromatosis type 2 that has material basis in homozygous mutation in the HAMP gene on chromosome 19q13
 * DOID:0111032
 * hemoglobin C
 * class of disease
 * hemoglobinopathy congenital hemolytic anemia disease
 * Human disease
 * DOID:2859
 * C15.378.071.141.150.490 C15.378.420.463 C16.320.070.490 C16.320.365.463
 * hemoglobin D disease
 * class of disease
 * hemoglobinopathy congenital hemolytic anemia
 * Human disease
 * DOID:5378
 * hemoglobin E
 * class of disease
 * hemoglobinopathy congenital hemolytic anemia
 * variant form of human hemoglobin
 * DOID:5379
 * D12.776.124.400.463.375 D12.776.422.316.762.426.375
 * hemoglobin H disease
 * class of disease
 * alpha thalassemia
 * alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other
 * DOID:0110031
 * hemoglobinopathy
 * class of disease
 * congenital hemolytic anemia genetic disease hemolytic anemia hemoglobin variant disease
 * genetic defect causing abnormal hemoglobin structure
 * DOID:2860
 * C15.378.420 C16.320.365
 * hemoglobinuria
 * class of disease
 * proteinuria hemolytic anemia disease
 * condition in which the oxygen transport protein hemoglobin is found in abnormally high concentrations in the urine
 * DOID:582
 * C12.777.934.734.634 C13.351.968.934.734.634 C23.888.942.750.634
 * 1GZX Haemoglobin.png
 * hemolytic-uremic syndrome
 * class of disease
 * kidney disease disease
 * Human disease
 * DOID:12554
 * C12.050.351.968.419.936.463 C12.200.777.419.936.463 C15.378.071.141.610 C15.378.140.855.925.500 C12.950.419.936.463 C15.378.243.937.925.500
 * Hemolytic-uremic syndrome
 * Schizocyte smear 2009-12-22.JPG
 * hemometra
 * class of disease
 * uterine disease menstrual disorder disease
 * Human disease
 * DOID:9958
 * C13.351.500.852.495
 * Hematometra
 * hemopericardium
 * class of disease
 * pericardial effusion
 * pericardial effusion that results from blood in the pericardial sac
 * DOID:11482
 * Hemopericardium
 * hemophagocytic lymphohistiocytosis
 * class of disease
 * lymphatic system disease disease
 * uncommon hematologic disorder seen more often in children than in adults
 * DOID:0050120
 * C15.604.250.410.575
 * Hemophagocytic lymphohistiocytosis
 * Hemophagocytic syndrome - cropped - very high mag.jpg
 * hemophilia A
 * class of disease symptom or sign
 * hemophilia coagulation factor deficiency X-linked recessive disease blood coagulation disease disease
 * X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged
 * DOID:12134
 * C15.378.100.100.500 C15.378.100.141.500 C15.378.463.500 C16.320.099.500
 * Hemophilia A
 * hemophilia B
 * class of disease
 * coagulation factor deficiency inherited blood coagulation disease X-linked recessive disease blood coagulation disease disease
 * An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
 * DOID:12259
 * C15.378.100.100.510 C15.378.100.141.510 C15.378.463.510 C16.320.099.510 C16.320.322.235
 * Hemophilia B
 * hemopneumothorax
 * class of disease
 * pneumothorax hemothorax disease
 * medical term describing the combination of two conditions: pneumothorax, or air in the chest cavity, and hemothorax (also called hæmothorax), or blood in the chest cavity
 * DOID:2718
 * C08.528.338 C23.550.414.904.500
 * hemorrhagic cystitis
 * class of disease
 * cystitis
 * Inflammation of the bladder resulting in bloody urine
 * DOID:0050859
 * C12.050.351.968.829.495.250 C12.200.777.829.495.250 C12.950.829.495.250
 * hemorrhagic disease
 * class of disease
 * blood coagulation disease disease
 * human disease
 * DOID:2213
 * C15.378.463
 * hemorrhoid
 * class of disease
 * gastrointestinal system disease pelvic varices anorectal disorder anal disease skin disease disease
 * vascular structures in the anal canal
 * DOID:9746
 * C06.405.469.860.401 C14.907.449
 * Hemorrhoids
 * Hemorrhoid.png
 * hemosiderosis
 * class of disease
 * iron overload iron metabolism disease disease
 * iron metabolism disease that has material basis in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload
 * DOID:12119
 * C18.452.565.500.500
 * Hemosiderosis
 * Hemosiderin1.jpg
 * hepatic angiomyolipoma
 * class of disease
 * liver neoplasm
 * Human disease
 * DOID:3317
 * hepatic flexure cancer
 * class of disease
 * ascending colon cancer
 * Human disease
 * DOID:260
 * hepatic hemangioma
 * class of disease
 * liver neoplasm hemangioma of intra-abdominal structure hemangioma hepatic vascular disease
 * non-cancerous tumor of the liver
 * DOID:271
 * Liver hemangioma
 * hepatic infarction
 * class of disease
 * hepatic vascular disease infarction ischemic hepatitis
 * Human disease
 * DOID:13738
 * C06.552.289 C23.550.513.355.500 C23.550.717.489.500
 * Hepatic infarction
 * hepatic osteogenic sarcoma
 * class of disease
 * extraosseous osteosarcoma liver cancer
 * Human disease
 * DOID:6370
 * hepatic vascular disease
 * class of disease
 * vascular disease liver disease
 * vascular disease that is located in the liver
 * DOID:272
 * hepatic veno-occlusive disease
 * class of disease
 * hepatic vascular disease vein disorder
 * hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver
 * DOID:0080177
 * C06.552.360 C14.907.460
 * hepatitis
 * class of disease symptom or sign
 * liver disease inflammation liver symptom disease
 * inflammation of the liver tissue
 * DOID:2237
 * C06.552.380
 * Hepatitis
 * Alcoholic hepatitis.jpg
 * hepatobiliary neoplasm
 * class of disease
 * gastrointestinal system benign neoplasm liver and intrahepatic bile duct neoplasm
 * gastrointestinal system neoplasm located in the hepatobiliary system
 * DOID:3117
 * hepatobiliary system cancer
 * class of disease
 * gastrointestinal system cancer liver and intrahepatic bile duct neoplasm
 * gastrointestinal system cancer that is located in the hepatobiliary system
 * DOID:0080355
 * hepatoblastoma
 * class of disease
 * liver cancer disease
 * uncommon malignant liver cancer occurring in infants and children
 * DOID:687
 * C04.557.435.380
 * Hepatoblastoma
 * Hepatoblastoma.jpg
 * hepatocellular adenoma
 * class of disease
 * liver neoplasm endocrine gland cancer benign neoplasms by histologic type adenoma disease
 * Hepatocellular adenoma (HA) is a rare benign tumor of the liver
 * DOID:0050868
 * C04.557.470.035.120 C04.588.274.623.040 C06.301.623.040 C06.552.697.040
 * Hepatic adenoma
 * Hepatic adenoma low mag.jpg
 * hepatocellular carcinoma
 * class of disease
 * liver carcinoma disease
 * liver carcinoma that has material basis in undifferentiated hepatocytes
 * DOID:684
 * C04.557.470.200.025.255 C04.588.274.623.160 C06.301.623.160 C06.552.697.160
 * Hepatocellular carcinoma
 * Hepatocellular carcinoma 1.jpg
 * hepatocellular clear cell carcinoma
 * class of disease
 * hepatocellular carcinoma clear cell carcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5016
 * hepatoid adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver
 * DOID:0060534
 * hepatoid pattern ovarian yolk sac tumor
 * class of disease
 * ovarian endodermal sinus tumor
 * Human disease
 * DOID:6512
 * hepatoid pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8195
 * hepatopulmonary syndrome
 * class of disease
 * liver disease
 * Human disease
 * DOID:900
 * C06.552.455 C08.381.385
 * hepatorenal syndrome
 * class of disease
 * acute kidney injury disease
 * Human disease
 * DOID:11823
 * C06.552.465 C12.777.419.291 C13.351.968.419.291
 * Hepatorenal syndrome
 * hereditary ataxia
 * class of disease
 * neurodegeneration
 * neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements
 * DOID:0050951
 * hereditary Wilms' tumor
 * class of disease
 * nephroblastoma inherited renal tumor
 * nephroblastoma that results in either bilateral disease or a family history of Wilms&#39; tumour
 * DOID:5183
 * hereditary alpha tryptasemia syndrome
 * class of disease
 * gene duplication disease syndrome
 * DOID:0080714
 * hereditary angioedema
 * class of disease symptom or sign
 * angioedema disease
 * Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain
 * DOID:14735
 * C14.907.079.500 C16.320.798.500.500 C17.800.862.945.066.500 C20.543.480.904.066.500 C20.673.795.500.500
 * Hereditary angioedema
 * Gezichtsoedeem.jpg
 * hereditary breast ovarian cancer
 * class of disease
 * autosomal dominant disease hereditary neoplastic syndromes syndrome disease
 * autosomal dominant disease characterized by the higher than normal tendency to develop breast and ovarian cancers in genetically related families
 * DOID:5683
 * C04.588.180.483 C04.588.322.455.431 C04.700.517 C13.351.500.056.630.705.431 C13.351.937.418.685.431 C16.320.700.517 C17.800.090.500.483 C19.344.410.431 C19.391.630.705.431
 * hereditary choroidal atrophy
 * class of disease
 * choroidal sclerosis
 * human disease
 * DOID:9794
 * hereditary combined deficiency of vitamin K-dependent clotting factors
 * class of disease
 * monogenic disease blood coagulation disease
 * human disease
 * DOID:0112172
 * hereditary conventional renal cell carcinoma
 * class of disease
 * hereditary renal cell carcinoma renal clear cell carcinoma
 * Human disease
 * DOID:7192
 * hereditary diffuse gastric cancer
 * class of disease
 * hereditary gastric cancer stomach cancer autosomal dominant disease diffuse gastric cancer
 * medical condition
 * DOID:0080764
 * hereditary lymphedema
 * class of disease
 * lymphedema Primary lymphedema disease
 * lymphedema commonly located in legs, caused by congenital abnormalities in the lymphatic system
 * DOID:0050580
 * hereditary lymphedema I
 * class of disease
 * hereditary lymphedema
 * hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood
 * DOID:0070212
 * hereditary lymphedema IA
 * class of disease
 * hereditary lymphedema genetic disease autosomal dominant disease
 * hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the FLT4 gene on chromosome 5q35
 * DOID:0070210
 * hereditary lymphedema IB
 * class of disease
 * hereditary lymphedema autosomal dominant disease
 * A hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in the chromosomal region 6q16.2-q22.1.
 * DOID:0070211
 * hereditary lymphedema IC
 * class of disease
 * hereditary lymphedema genetic disease autosomal dominant disease
 * hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the GJC2 gene on chromosome 1q42
 * DOID:0070208
 * hereditary lymphedema ID
 * class of disease
 * hereditary lymphedema genetic disease autosomal dominant disease
 * hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the VEGFC gene on chromosome 4q34
 * DOID:0070209
 * hereditary lymphedema II
 * class of disease
 * hereditary lymphedema autosomal dominant disease
 * hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance
 * DOID:0070213
 * hereditary mixed polyposis syndrome 1
 * class of disease
 * hereditary mixed polyposis syndrome chromosomal duplication syndrome
 * human disease
 * DOID:0111685
 * hereditary motor and sensory neuropathy
 * class of disease
 * congenital disorder Sensorimotor neuropathy peripheral neuropathy hereditary peripheral neuropathy
 * congenital disorder of nervous system
 * DOID:2477
 * C10.500.300 C10.574.500.495 C10.668.829.800.300 C16.131.666.300 C16.320.400.375
 * Hereditary motor and sensory neuropathies
 * hereditary neutrophilia
 * class of disease
 * leukocyte disease neutrophilia rare genetic immune disease genetic hematologic disease genetic disease autosomal dominant disease
 * human disease
 * DOID:0090120
 * hereditary night blindness
 * class of disease
 * night blindness
 * Human disease
 * DOID:8498
 * hereditary nonpolyposis colorectal cancer type 2
 * class of disease
 * Lynch syndrome
 * A Lynch syndrome that has material basis in mutations in the MLH1 gene on chromosome 3p22.2.
 * DOID:0070274
 * hereditary nonpolyposis colorectal cancer type 4
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutation in the PMS2 gene on chromosome 7p22
 * DOID:0070275
 * hereditary nonpolyposis colorectal cancer type 5
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutation in the MSH6 gene on chromosome 2p16
 * DOID:0070272
 * hereditary nonpolyposis colorectal cancer type 6
 * class of disease
 * Lynch syndrome
 * Lynch syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p22
 * DOID:0070273
 * hereditary nonpolyposis colorectal cancer type 7
 * class of disease
 * Lynch syndrome
 * A Lynch syndrome that has material basis in mutation in the MLH3 gene on chromosome 14q24.3.
 * DOID:0070276
 * hereditary nonpolyposis colorectal cancer type 8
 * class of disease
 * Lynch syndrome chromosomal deletion syndrome
 * human disease
 * DOID:0070270
 * hereditary papulotranslucent acrokeratoderma
 * class of disease
 * cholesteatoma
 * keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis
 * DOID:0060360
 * hereditary renal cell carcinoma
 * class of disease
 * renal cell carcinoma inherited renal tumor
 * human disease
 * DOID:4455
 * hereditary retinal dystrophy
 * class of disease
 * fundus dystrophy genetic disease hereditary eye disease
 * Human disease
 * DOID:8500
 * hereditary sensory and autonomic neuropathy
 * class of disease
 * hereditary disorder peripheral neuropathy
 * congenital disorder of nervous system
 * DOID:0050548
 * C10.500.250 C10.574.500.493 C10.668.829.800.175 C16.131.666.310 C16.320.400.415
 * hereditary sensory and autonomic neuropathy type 1
 * class of disease
 * hereditary sensory and autonomic neuropathy
 * hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance
 * DOID:0070162
 * hereditary sensory and autonomic neuropathy type 1A
 * class of disease
 * hereditary sensory and autonomic neuropathy type 1 genetic disease autosomal dominant disease
 * hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has material basis in heterozygous mutation in the SPTLC1 gene on chromosome 9q22
 * DOID:0070152
 * hereditary sensory and autonomic neuropathy type 2
 * class of disease
 * hereditary sensory and autonomic neuropathy
 * hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood
 * DOID:0070161
 * hereditary sensory neuropathy X-linked
 * class of disease
 * hereditary sensory and autonomic neuropathy X-linked recessive disease
 * hereditary sensory neuropathy characterized by X-linked inheritance of slowly progressing neuropathy with onset in the first or second decade of life
 * DOID:0070159
 * hereditary sensory neuropathy type 1B
 * class of disease
 * hereditary sensory and autonomic neuropathy genetic disease autosomal dominant disease
 * hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has material basis in variation in the chromosome region 3p24-p22
 * DOID:0070148
 * hereditary spastic paraplegia 14
 * class of disease
 * hereditary spastic paraplegia pure or complex autosomal recessive spastic paraplegia autosomal recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 3q27-q28
 * DOID:0110767
 * hereditary spastic paraplegia 16
 * class of disease
 * hereditary spastic paraplegia pure or complex X-linked spastic paraplegia X-linked recessive disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2.
 * DOID:0110769
 * hereditary spastic paraplegia 19
 * class of disease
 * hereditary spastic paraplegia autosomal dominant pure spastic paraplegia autosomal dominant disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 9q
 * DOID:0110772
 * hereditary spastic paraplegia 24
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 13q14
 * DOID:0110775
 * hereditary spastic paraplegia 25
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 6q23-q24.1.
 * DOID:0110776
 * hereditary spastic paraplegia 27
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 10q22.1-q24.1.
 * DOID:0110778
 * hereditary spastic paraplegia 29
 * class of disease
 * hereditary spastic paraplegia autosomal dominant complex spastic paraplegia autosomal dominant disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1.
 * DOID:0110780
 * hereditary spastic paraplegia 32
 * class of disease
 * hereditary spastic paraplegia autosomal recessive complex spastic paraplegia autosomal recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 14q12-q21
 * DOID:0110783
 * hereditary spastic paraplegia 34
 * class of disease
 * hereditary spastic paraplegia X-linked pure spastic paraplegia X-linked recessive disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq24-q25
 * DOID:0110785
 * hereditary spastic paraplegia 36
 * class of disease
 * hereditary spastic paraplegia autosomal dominant complex spastic paraplegia autosomal dominant disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 12q23-q24
 * DOID:0110787
 * hereditary spastic paraplegia 37
 * class of disease
 * hereditary spastic paraplegia autosomal dominant pure spastic paraplegia autosomal dominant disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 8p21.1-q13.3.
 * DOID:0110788
 * hereditary spastic paraplegia 38
 * class of disease
 * hereditary spastic paraplegia autosomal dominant complex spastic paraplegia autosomal dominant disease
 * hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15
 * DOID:0110789
 * hereditary spastic paraplegia 41
 * class of disease
 * hereditary spastic paraplegia autosomal dominant pure spastic paraplegia autosomal dominant disease
 * A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2.
 * DOID:0110793
 * hereditary spherocytosis
 * class of disease
 * congenital hemolytic anemia spherocytosis disease
 * congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape
 * DOID:12971
 * C15.378.071.141.150.785 C16.320.070.785
 * Hereditary spherocytosis
 * hereditary spherocytosis type 3
 * class of disease
 * hereditary spherocytosis genetic disease autosomal recessive disease
 * A hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.
 * DOID:0110918
 * hernia of ovary and fallopian tube
 * class of disease
 * female reproductive system disease
 * Human disease
 * DOID:12735
 * heroin dependence
 * class of disease
 * opiate dependence
 * opiate dependence that involves the continued use of heroin despite problems related to use of the substance
 * DOID:9976
 * C25.775.675.400
 * herpes gestationis
 * class of disease
 * vesiculobullous skin disease dermatosis of pregnancy pemphigoid autoimmune skin disease disease
 * dermatosis of pregnancy
 * DOID:14482 DOID:0040098
 * C13.703.570 C17.800.865.700
 * Gestational pemphigoid
 * Pemphigoid gestationis - high mag.jpg
 * hexahydrophthalic anhydride allergic asthma
 * class of disease
 * allergic asthma
 * allergic asthma that has allergic trigger hexahydrophthalic anhydride
 * DOID:0040051
 * hexamethylene diisocyanate allergic asthma
 * class of disease
 * isocyanates allergic asthma
 * allergic asthma to isocyanates that has allergic trigger hexamethylene diisocyanate
 * DOID:0040040
 * hidradenitis
 * class of disease
 * sweat gland disease
 * human disease
 * DOID:2282
 * C17.800.946.315
 * hidradenoma
 * class of disease
 * sweat gland neoplasm epithelial skin neoplasm benign neoplasms by histologic type
 * human disease
 * DOID:3896
 * C04.557.470.035.175 C04.557.470.550.175
 * Hidradenoma
 * hidrocystoma
 * class of disease
 * apocrine sweat gland neoplasm benign neoplasm of sweat gland
 * Human disease
 * DOID:3893
 * C04.557.470.035.175.375 C04.557.470.550.175.375
 * Hidrocystoma
 * high pressure neurological syndrome
 * class of disease
 * central nervous system disease diving disorder
 * neurological and physiological disorder experienced by divers
 * DOID:3230
 * C10.228.566 C24.410
 * hilar lung carcinoma
 * class of disease
 * lung carcinoma lung hilum cancer
 * Human disease
 * DOID:8207
 * hilar lung neoplasm
 * class of disease
 * lung benign neoplasm
 * Human disease
 * DOID:5767
 * histidine metabolism disease
 * class of disease
 * amino acid metabolic disorder
 * amino acid metabolic disorder that involves deficiency in histidine
 * DOID:9265
 * histidinemia
 * class of disease
 * histidine metabolism disease
 * histidine metabolism disease that involves a deficiency of the enzyme histidase
 * DOID:0060168
 * L-histidine-skeletal.png
 * histiocytic and dendritic cell cancer
 * class of disease
 * hematologic cancer lymphoid hemopathy
 * sarcoma and hematologic cancer that derives from follicular lymphoma
 * DOID:5621
 * histiocytoid hemangioma
 * class of disease
 * hemangioma
 * Human disease
 * DOID:474
 * histiocytoma
 * class of disease
 * connective tissue neoplasm connective tissue benign neoplasm
 * Human disease
 * DOID:4231
 * C04.557.450.565.590.425
 * Histiocytoma
 * histiocytosis
 * class of disease
 * lymphatic system disease disease
 * lymphatic system disease that is characterized by an excessive number of histiocytes
 * DOID:3405
 * C15.604.250
 * Histiocytoses
 * histoplasmosis
 * class of disease
 * primary systemic mycosis genetic disease disease
 * human disease
 * DOID:1731
 * C01.150.703.450
 * Histoplasmosis
 * Histoplasmosis capsulatum.jpg
 * histoplasmosis meningitis
 * class of disease
 * fungal meningitis histoplasmosis
 * Human disease
 * DOID:12246
 * histoplasmosis retinitis
 * class of disease
 * retinitis
 * Human disease
 * DOID:11316
 * Presumed ocular histoplasmosis syndrome
 * histrionic personality disorder
 * class of disease
 * personality disorder disease
 * personality disorder characterized by excessive emotionality and attention-seeking
 * DOID:334
 * F03.675.400
 * Histrionic personality disorder
 * hole retinal cyst
 * class of disease
 * degeneration of macula and posterior pole retinoschisis and retinal cysts retinal perforation
 * Human disease
 * DOID:13214
 * holoprosencephaly
 * class of disease symptom or sign
 * nervous system malformations syndrome disease
 * congenital disorder of the nervous system
 * DOID:4621
 * C05.660.207.410 C10.500.034.875 C16.131.077.410 C16.131.260.380 C16.131.621.207.410 C16.131.666.034.875 C16.320.180.380
 * Holoprosencephaly
 * Alobar holoprosencephaly.jpg
 * holoprosencephaly 1
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * A holoprosencephaly that has material basis in variation in the chromosome region 21q22.3.
 * DOID:0110881
 * holoprosencephaly 2
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * holoprosencephaly that has material basis in mutation in the homeobox-containing SIX3 gene on chromosome 2p21
 * DOID:0110872
 * holoprosencephaly 5
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * holoprosencephaly that has material basis in heterozygous mutation in the ZIC2 gene on chromosome 13q32
 * DOID:0110878
 * holoprosencephaly 6
 * class of disease
 * holoprosencephaly genetic disease
 * A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.
 * DOID:0110874
 * holoprosencephaly 8
 * class of disease
 * holoprosencephaly genetic disease
 * holoprosencephaly that has material basis in variation in the chromosome region 14q13
 * DOID:0110879
 * holoprosencephaly 9
 * class of disease
 * holoprosencephaly genetic disease autosomal dominant disease
 * holoprosencephaly that has material basis in heterozygous mutation in the GLI2 gene on chromosome 2q14
 * DOID:0110873
 * homocarnosinosis
 * class of disease
 * gamma-amino butyric acid metabolism disorder inborn disorder of peptide metabolism encephalopathy
 * gamma-amino butyric acid metabolism disorder that is characterized by an excess of homocarnosine in the brain and has material basis in a deficiency of serum carnosinase in its ability to hydrolyze homocarnosine
 * DOID:0060177
 * hordeolum
 * class of disease symptom or sign
 * blepharitis eyelid disease disease
 * bacterial infection of an oil gland in the eyelid
 * DOID:9909
 * C01.150.252.289.400 C01.375.354.400 C11.294.354.400 C11.338.648
 * Stye
 * Stye02.jpg
 * hordeolum externum
 * class of disease
 * blepharitis
 * human disease
 * DOID:13134
 * horned turban snail allergy
 * class of disease
 * snail allergy
 * snail allergy triggered by Turbo cornutus
 * DOID:0060531
 * human cytomegalovirus infection
 * class of disease
 * viral infectious disease cytomegaloviral disease
 * human disease
 * DOID:0080827
 * human immunodeficiency virus infectious disease
 * class of disease
 * viral infectious disease Lentivirus infectious disease
 * disease affecting the human immune system
 * DOID:526
 * C20.673.480 C01.778.640.400 C01.925.782.815.616.400 C01.925.813.400 C01.221.250.875 C01.221.812.640.400 C12.100.937.640.400
 * human monocytic ehrlichiosis
 * class of disease
 * ehrlichiosis disease
 * human disease
 * DOID:0050026
 * Echaff.jpg
 * humeroradial synostosis
 * class of disease
 * synostosis
 * Human disease
 * DOID:0060467
 * hyaline body myopathy
 * class of disease
 * congenital myopathy
 * human disease
 * DOID:0111267
 * hyaline fibromatosis syndrome
 * class of disease
 * autosomal recessive disease connective tissue disease fibromatosis
 * human disease
 * DOID:0111669
 * hyalinizing trabecular adenoma
 * class of disease
 * follicular adenoma thyroid adenoma
 * human disease
 * DOID:6203
 * hydranencephaly with renal aplasia-dysplasia
 * class of disease
 * genetic disease autosomal recessive disease syndrome
 * human disease
 * DOID:0080327
 * hydrocele
 * class of disease
 * male reproductive system disease
 * human disease
 * DOID:9912
 * C12.294.882
 * Hydrocele
 * Gray1148.png
 * hydrolethalus syndrome 1
 * class of disease
 * hydrolethalus syndrome
 * human disease
 * DOID:0111355
 * hydrolethalus syndrome 2
 * class of disease
 * hydrolethalus syndrome
 * human disease
 * DOID:0111356
 * hydronephrosis
 * class of disease
 * urinary tract obstruction kidney disease disease
 * human disease
 * DOID:11111
 * C12.777.419.307 C13.351.968.419.307
 * Hydronephrosis
 * hydrophthalmos
 * class of disease
 * primary congenital glaucoma
 * Human disease
 * DOID:11212
 * C11.250.480 C11.525.381.407.480 C16.131.384.480 C16.614.438
 * hydrops of gallbladder
 * class of disease
 * gallbladder disease
 * Human disease
 * DOID:9717
 * hyper IgE recurrent infection syndrome 2
 * class of disease
 * autosomal recessive disease Job's syndrome
 * human disease
 * DOID:0080594
 * hyper IgE recurrent infection syndrome 3
 * class of disease
 * Job's syndrome autosomal recessive disease
 * human disease
 * DOID:0080595
 * hyper IgE recurrent infection syndrome 4
 * class of disease
 * autosomal recessive disease Job's syndrome
 * human disease
 * DOID:0080596
 * hyper-IgM syndrome type 4
 * class of disease
 * hyper IgM syndrome hyperimmunoglobulin syndrome
 * hyperimmunoglobulin syndrome characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process
 * DOID:0060760
 * hyperalphalipoproteinemia 1
 * class of disease
 * cholesterol-ester transfer protein deficiency autosomal dominant disease hyperalphalipoproteinemia
 * human disease
 * DOID:0111369
 * hyperandrogenism
 * class of disease
 * gonadal disease sex differentiation disease disease
 * medical condition characterized by excessive levels of androgens in the body
 * DOID:11613
 * C12.050.351.875.253.064.500 C12.050.351.875.253.090.750 C16.131.939.316.064.500 C16.131.939.316.129.750 C19.391.119.064.500 C19.391.119.090.750 C12.200.706.316.064.500 C12.200.706.316.090.750 C12.800.316.064.500 C12.800.316.090.750
 * Hyperandrogenism
 * hypercalcemia
 * class of disease
 * calcium metabolism disease disease
 * high calcium (Ca2+) level in the blood serum
 * DOID:12678
 * C18.452.174.451 C18.452.950.340
 * Hypercalcemia
 * hypercalcemic sarcoidosis
 * class of disease
 * sarcoidosis hypercalcemia
 * Human disease
 * DOID:13407
 * hypercalcemic type ovarian small cell carcinoma
 * class of disease
 * ovarian small cell carcinoma
 * Human disease
 * DOID:7651
 * hypercementosis
 * class of disease
 * teeth hard tissue disease
 * Human disease
 * DOID:12733
 * C07.793.422
 * hyperekplexia 1
 * class of disease
 * hyperekplexia genetic disease autosomal recessive disease autosomal dominant disease
 * hyperekplexia that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the GLRA1 gene on chromosome 5q32
 * DOID:0060696
 * C10.228.590
 * hyperekplexia 4
 * class of disease
 * hyperekplexia autosomal recessive disease
 * hyperekplexia that is characterized by extreme hypertonia, stiff and rigid appeareance and that has material basis in homozygous mutation in the ATAD1 gene on chromosome 10q23
 * DOID:0080581
 * hyperglobulinemic purpura
 * class of disease
 * purpura
 * Human disease
 * DOID:3325
 * C14.907.454.550 C15.378.100.802.250 C15.378.463.515.550 C23.550.414.950.250 C23.888.885.687.250
 * hyperglycemia
 * class of disease abnormally high value
 * glucose metabolism disease disease
 * human disease
 * DOID:4195
 * C18.452.394.952
 * Hyperglycemia
 * Hyperglycemia.png
 * hyperhomocysteinemia
 * class of disease
 * sulfuraminoacidemia amino acid metabolic disorder disease
 * amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood
 * DOID:9279
 * C16.320.565.100.480 C18.452.603.378 C18.452.648.100.480 C18.654.521.500.133.699.418
 * L-Homocysteine.svg
 * hyperimmunoglobulin syndrome
 * class of disease
 * B cell deficiency
 * Human disease
 * DOID:2959
 * hyperinsulinemia
 * class of disease
 * endocrine pancreas disease glucose metabolism disease pancreas disease
 * condition in which there are excess levels of insulin circulating in the blood relative to the level of glucose
 * DOID:2018
 * hyperlipoproteinemia type IV
 * class of disease
 * hyperlipidemia familial hyperlipidemia
 * human disease
 * DOID:1172
 * C16.320.565.398.487 C18.452.584.500.500.644.490 C18.452.584.500.500.851.500 C18.452.648.398.487 C18.452.584.563.487
 * hypermanganesemia with dystonia
 * class of disease
 * metal metabolism disorder
 * metal metabolism disorder that is characterized by involuntary, sustained muscle contractions (dystonia) and other uncontrolled movements resulting from excessive accumulation of manganese
 * DOID:0080535
 * hypermanganesemia with dystonia 1
 * class of disease
 * hypermanganesemia with dystonia
 * human disease
 * DOID:0080536
 * hypermethioninemia
 * class of disease
 * amino acid metabolic disorder
 * An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body.
 * DOID:0050544
 * hypermobility of coccyx
 * class of disease
 * spondyloarthropathy
 * Human disease
 * DOID:12537
 * hypermobility syndrome
 * class of disease
 * arthropathy joint hypermobility disease
 * human disease: joints that stretch farther than normal
 * DOID:13781
 * Hypermobility
 * Doublejointedfinger.JPG
 * hyperopia
 * class of disease symptom or sign
 * refractive error disease
 * visual defect which causes to see the far objects clearly and near objects unclearly
 * DOID:9834
 * C11.744.479
 * Hyperopia
 * Hypermetropia.svg
 * hyperostosis
 * class of disease
 * bone remodeling disease disease
 * human disease
 * DOID:205
 * C05.116.540
 * Hyperostosis
 * hyperphosphatemia
 * class of disease
 * phosphorus metabolism disease genetic disease disease
 * electrolyte disorder in which there is an elevated level of phosphate in the blood.
 * DOID:0050459
 * C18.452.750.199
 * Hyperphosphatemia
 * hyperphosphatemic familial tumoral calcinosis
 * class of disease
 * calcinosis genetic disease Tumoral calcinosis autosomal recessive disease
 * human disease
 * DOID:0111063
 * hyperpigmentation of eyelid
 * class of disease
 * pigmentation disorder eyelid disease
 * Human disease
 * DOID:10122
 * hyperpituitarism
 * class of disease
 * pituitary gland disease anterior pituitary gland disease disease
 * endocrine disease
 * DOID:2444
 * C10.228.140.617.738.250 C19.700.355
 * hyperprolinemia type 1
 * class of disease
 * hyperprolinemia autosomal recessive disease
 * hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the proline dehydrogenase gene on chromosome 22q11
 * DOID:0080542
 * hyperprolinemia type 2
 * class of disease
 * hyperprolinemia autosomal recessive disease
 * hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36
 * DOID:0080543
 * hyperprothrombinemia
 * class of disease
 * thrombophilia autosomal dominant disease
 * human disease
 * DOID:0080701
 * hypersecretion glaucoma
 * class of disease
 * glaucoma
 * Human disease
 * DOID:11148
 * hypersensitivity vasculitis
 * class of disease
 * type III hypersensitivity
 * Human disease
 * DOID:9809
 * C14.907.940.910 C20.543.520.910
 * hypersomnia
 * class of disease symptom or sign
 * sleep disorder neurological disorder sleep disturbance disease
 * excessive sleep
 * DOID:8619
 * C10.886.425.800.200 F03.870.400.800.200
 * hypersplenism
 * class of disease
 * splenic disease disease
 * Human disease
 * DOID:6376
 * C15.604.744.293
 * hypertensive encephalopathy
 * class of disease
 * intracranial hypertension encephalomyelitis disease
 * general brain dysfunction due to significantly high blood pressure
 * DOID:9427
 * C10.228.140.631.500
 * hypertensive retinopathy
 * class of disease
 * retinal disease complications of hypertension disease
 * Human disease
 * DOID:11561
 * C11.768.346 C14.907.489.815
 * Hypertensive retinopathy
 * Hypertensiveretinopathy.jpg
 * hyperthecosis
 * class of disease
 * ovarian disease
 * hyperplasia of the theca interna of the ovary
 * DOID:7347
 * hypertrichosis
 * class of disease
 * hair diseases epidermal disease genetic hair anomaly disease
 * hair disease characterized by hair growth that is abnormal in quantity or location
 * DOID:420
 * C17.800.329.875
 * Hypertrichosis
 * Alice Teennager.JPG
 * hypertrichosis of eyelid
 * class of disease
 * eyelid degenerative disease hypertrichosis nervous system heredodegenerative disease eyelid disease
 * hypertrichosis (disease) that involves the eyelid
 * DOID:11669
 * hypertrophic cardiomyopathy 1
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYH7 gene on chromosome 14q12
 * DOID:0110307
 * hypertrophic cardiomyopathy 10
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene
 * DOID:0110316
 * hypertrophic cardiomyopathy 11
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the ACTC1 gene on chromosome 15q14
 * DOID:0110317
 * hypertrophic cardiomyopathy 12
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the CSRP3 gene on chromosome 11p15
 * DOID:0110318
 * hypertrophic cardiomyopathy 13
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21
 * DOID:0110319
 * hypertrophic cardiomyopathy 14
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in mutation in the MYH6 gene
 * DOID:0110320
 * hypertrophic cardiomyopathy 15
 * class of disease
 * familial hypertrophic cardiomyopathy
 * human disease
 * DOID:0110321
 * hypertrophic cardiomyopathy 16
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26
 * DOID:0110322
 * hypertrophic cardiomyopathy 17
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12
 * DOID:0110323
 * hypertrophic cardiomyopathy 18
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
 * DOID:0110324
 * hypertrophic cardiomyopathy 2
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)
 * DOID:0110308
 * hypertrophic cardiomyopathy 20
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
 * DOID:0110326
 * hypertrophic cardiomyopathy 21
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.
 * DOID:0110311
 * hypertrophic cardiomyopathy 25
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TCAP gene on chromosome 17q12
 * DOID:0110328
 * hypertrophic cardiomyopathy 3
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22
 * DOID:0110309
 * hypertrophic cardiomyopathy 4
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11
 * DOID:0110310
 * hypertrophic cardiomyopathy 6
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2)
 * DOID:0110312
 * hypertrophic cardiomyopathy 7
 * class of disease
 * familial hypertrophic cardiomyopathy
 * A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
 * DOID:0110313
 * hypertrophic cardiomyopathy 8
 * class of disease
 * familial hypertrophic cardiomyopathy
 * hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene
 * DOID:0110314
 * hypertrophic elongation of cervix
 * class of disease
 * cervix disease
 * Human disease
 * DOID:2251
 * hypertrophic pyloric stenosis
 * class of disease
 * pyloric stenosis
 * pyloric stenosis characterized by the enlargement of the muscle surrounding the pylorus, causing severe projectile non-bilious vomiting
 * DOID:12638
 * C06.405.748.340.690.500
 * hypertrophy of tongue papillae
 * class of disease
 * tongue disease
 * Human disease
 * DOID:13333
 * hypertropia
 * class of disease
 * strabismus disease
 * Human disease
 * DOID:9837
 * Hypertropia
 * hyperuricemia
 * class of disease
 * acquired metabolic disease disease
 * acquired metabolic disease that has material basis in an abnormally high level of uric acid in the blood.
 * DOID:1920
 * C23.550.449
 * Hyperuricemia
 * hypervitaminosis A
 * class of disease
 * overnutrition hypervitaminosis disease
 * Human disease
 * DOID:9972
 * C18.654.301
 * All-trans-Retinol2.svg
 * hypervitaminosis D
 * class of disease
 * overnutrition hypervitaminosis disease
 * excess of Vitamin D leading to abnormalities
 * DOID:9971
 * hypoactive sexual desire disorder
 * class of disease
 * psychosexual disorder sexual dysfunction disease
 * sexual dysfunction
 * DOID:13868
 * F03.835
 * hypobetalipoproteinemia
 * class of disease
 * hypolipoproteinemia disease
 * hypolipoproteinemia characterized by permanently low levels of apolipoprotein B and LDL cholesterol resulting from an impaired ability to absorb and transport fats
 * DOID:1390
 * C16.320.565.398.500.440 C18.452.584.500.875.440 C18.452.648.398.500.440 C18.452.584.563.500.440
 * hypochondriasis
 * class of disease
 * somatoform disorder nosophobia disease
 * somatoform disorder that involves an excessive preoccupation or worry about having a serious illness
 * DOID:12883
 * F03.875.450
 * hypochondrogenesis
 * class of disease
 * osteochondrodysplasia achondrogenesis genetic disease spinal disease monogenic disease
 * human disease
 * DOID:0080044
 * hypochromic anemia
 * class of disease
 * anemia
 * generic term for any type of anemia in which the red blood cells (erythrocytes) are paler than normal
 * DOID:11759
 * C15.378.071.196
 * hypoglossal nerve disease
 * class of disease
 * glossopharyngeal nerve disease
 * human disease
 * DOID:13814
 * C10.292.525
 * hypoglossal nerve neoplasm
 * class of disease
 * cranial nerve neoplasm hypoglossal nerve disease
 * Human disease
 * DOID:3198
 * hypoglycemic coma
 * class of disease
 * encephalopathy coma hypoglycemia
 * human disease
 * DOID:1607
 * hypogonadism
 * class of disease
 * gonadal disease disease
 * endocrine disease
 * DOID:1924
 * C19.391.482
 * Hypogonadism
 * hypogonadotropic hypogonadism 12 with or without anosmia
 * class of disease
 * hypogonadotropic hypogonadism genetic disease
 * hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21
 * DOID:0090072
 * hypogonadotropic hypogonadism 16 with or without anosmia
 * class of disease
 * hypogonadotropic hypogonadism genetic disease autosomal dominant disease
 * hypogonadotropic hypogonadism that has material basis in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes
 * DOID:0090080
 * hypogonadotropic hypogonadism 2 with or without anosmia
 * class of disease
 * hypogonadotropic hypogonadism genetic disease
 * hypogonadotropic hypogonadism that has material basis in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes
 * DOID:0090083
 * hypohidrosis
 * class of disease
 * sweat gland disease abnormal sudomotor regulation
 * Human disease
 * DOID:11155
 * C17.800.946.370
 * hypolipoproteinemia
 * class of disease
 * lipid metabolism disorder disease
 * Human disease
 * DOID:1387
 * C16.320.565.398.500 C18.452.584.500.875 C18.452.648.398.500 C18.452.584.563.500
 * hypomyelinating leukodystrophy
 * class of disease
 * leukodystrophy Hereditary CNS demyelinating disease
 * leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system
 * DOID:0060786
 * hypomyelinating leukodystrophy 14
 * class of disease
 * hypomyelinating leukodystrophy autosomal recessive disease
 * human disease
 * DOID:0080296
 * hypomyelinating leukoencephalopathy
 * class of disease
 * spinocerebellar ataxia
 * Human disease
 * DOID:0050987
 * hypoparathyroidism, familial isolated
 * class of disease
 * genetic hypoparathyroidism hypoparathyroidism
 * human disease
 * DOID:0111387
 * hypopharynx cancer
 * class of disease
 * carcinoma pharyngeal cancer neoplasm of hypopharynx
 * pharynx cancer that is located in the hypopharynx
 * DOID:8533
 * Hypopharyngeal cancer
 * HypopharynxCa.jpg
 * hypophosphatemic nephrolithiasis/osteoporosis
 * class of disease
 * kidney disease familial hypophosphatemia
 * human disease
 * DOID:0080655
 * hypopigmentation of eyelid
 * class of disease
 * eyelid degenerative disease pigmentation disorder eyelid disease
 * human disease
 * DOID:11668
 * hypopyon
 * class of disease symptom or sign
 * iridocyclitis eye symptom disease
 * Human disease
 * DOID:10443
 * Hypopyon
 * Hypopyon.jpg
 * hypopyon ulcer
 * class of disease
 * hypopyon corneal ulcer
 * Human disease
 * DOID:10442
 * hypospadias
 * class of disease
 * non-syndromic urogenital tract malformation of male penile disease congenital disorder disease
 * condition in which the urethra does not open from the head of the penis
 * DOID:10892
 * C12.294.494.400 C12.706.516 C13.351.875.466 C16.131.939.516
 * Hypospadias
 * Hypospadias3.jpg
 * hypothalamic disease
 * class of disease
 * thalamic disease encephalopathy
 * human disease
 * DOID:1931
 * C10.228.140.617
 * hypothalamic neoplasm
 * class of disease
 * diencephalic neoplasm brain cancer connective tissue neoplasm hypothalamic disease
 * human disease
 * DOID:3644
 * C04.588.614.250.195.885.500 C10.228.140.211.885.500 C10.228.140.617.477 C10.551.240.250.700.500
 * hypothyroidism
 * class of disease
 * thyroid gland disease disease
 * human disease
 * DOID:1459
 * C19.874.482
 * Hypothyroidism
 * hypotonia-cystinuria syndrome
 * class of disease
 * syndrome cystinuria chromosomal deletion syndrome
 * human disease
 * DOID:0060858
 * hypotrichosis 1
 * class of disease
 * hypotrichosis genetic disease autosomal dominant disease
 * A hypotrichosis that has material basis in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.
 * DOID:0110698
 * hypotrichosis 10
 * class of disease
 * hypotrichosis genetic disease autosomal recessive disease
 * A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.
 * DOID:0110707
 * hypotrichosis 14
 * class of disease
 * hypotrichosis simplex hypotrichosis
 * human disease
 * DOID:0080582
 * hypotrichosis 4
 * class of disease
 * hypotrichosis genetic disease autosomal dominant disease
 * A hypotrichosis that has material basis in a autosomal dominant mutation of HR on chromosome 8p21.3.
 * DOID:0110701
 * hypotrichosis 5
 * class of disease
 * hypotrichosis genetic disease autosomal dominant disease
 * A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3.
 * DOID:0110702
 * hypotrichosis 9
 * class of disease
 * hypotrichosis genetic disease autosomal recessive disease
 * A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 10q11.23-q22.3.
 * DOID:0110706
 * hypotrichosis of eyelid
 * class of disease
 * eyelid degenerative disease hypotrichosis eyelid disease
 * hypotrichosis that involves the eyelid
 * DOID:11671
 * hypotropia
 * class of disease
 * strabismus
 * Human disease
 * DOID:9841
 * ichthyosis follicularis-alopecia-photophobia syndrome 1
 * class of disease
 * X-linked recessive disease syndrome Ichthyosis follicularis with alopecia and photophobia syndrome
 * human disease
 * DOID:0111821
 * ideomotor apraxia
 * class of disease
 * apraxia
 * Human disease
 * DOID:4627
 * C10.597.606.881.350.200 C23.888.592.604.882.350.200 F01.700.875.350.200
 * idiopathic corneal edema
 * class of disease
 * corneal edema
 * Human disease
 * DOID:11033
 * idiopathic generalized epilepsy 11
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111312
 * idiopathic generalized epilepsy 12
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111313
 * idiopathic generalized epilepsy 13
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111314
 * idiopathic generalized epilepsy 14
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111315
 * idiopathic generalized epilepsy 15
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111316
 * idiopathic generalized epilepsy 2
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111317
 * idiopathic generalized epilepsy 3
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111318
 * idiopathic generalized epilepsy 4
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111319
 * idiopathic generalized epilepsy 5
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111320
 * idiopathic generalized epilepsy 7
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111321
 * idiopathic generalized epilepsy 9
 * class of disease
 * generalized epilepsy
 * human disease
 * DOID:0111323
 * idiopathic orbital inflammatory disease
 * class of disease
 * orbital granuloma chronic orbital inflammation
 * Human disease
 * DOID:9369
 * C11.675.679
 * Inflammatory pseudotumor - Plasma cell granuloma Case 176 (5601449638).jpg
 * idiopathic peripheral autonomic neuropathy
 * class of disease
 * autonomic nervous system disease autonomic peripheral neuropathy
 * human disease
 * DOID:11488
 * idiopathic progressive polyneuropathy
 * class of disease
 * polyneuropathy
 * human disease
 * DOID:10593
 * idiopathic pulmonary fibrosis
 * class of disease
 * idiopathic interstitial pneumonia pulmonary fibrosis
 * chronic, irreversible and ultimately fatal disease characterized by a progressive decline in lung function
 * DOID:0050156
 * C08.381.483.487.500 C08.381.765.500
 * Idiopathic pulmonary fibrosis
 * idiopathic scoliosis
 * class of disease
 * scoliosis
 * scoliosis with no known cause
 * DOID:0060250
 * ileal neoplasm
 * class of disease
 * small intestine neoplasm ileal disease
 * human disease
 * DOID:10156
 * C04.588.274.476.411.501 C06.301.371.411.501 C06.405.249.411.501 C06.405.469.420.501 C06.405.469.491.501
 * ileitis
 * class of disease
 * Crohn's disease enteritis
 * inflammatory bowel disease characterized by inflammation located in ileum, has symptom diarrhea, has symptom abdominal pain, often in the right lower quadrant, has symptom weight loss
 * DOID:0060189
 * C06.405.205.462.624 C06.405.469.326.875 C06.405.469.420.520
 * Ileitis
 * ileum cancer
 * class of disease
 * small intestine cancer ileal neoplasm
 * small intestine cancer that is located in the ileum
 * DOID:10153
 * ileus
 * class of disease
 * bowel obstruction disease
 * human disease characterized by impairment of intestinal peristalsis; in modern language usually excludes mechanical bowel obstruction
 * DOID:8440
 * C06.405.469.531.492
 * Ileus
 * iliac vein thrombophlebitis
 * class of disease
 * thrombophlebitis
 * Human disease
 * DOID:10880
 * immature cataract
 * class of disease
 * senile cataract
 * Human disease
 * DOID:10997
 * immature teratoma
 * class of disease
 * teratoma
 * Human disease
 * DOID:5563
 * immature teratoma of ovary
 * class of disease
 * malignant ovarian germ cell neoplasm malignant non-dysgerminomatous germ cell tumor of ovary ovarian biphasic or triphasic teratoma
 * Human disease
 * DOID:6331
 * immune disorder
 * class of disease
 * disease of anatomical entity
 * a disease of the immune system
 * DOID:2914
 * C20
 * Diseases and disorders of the immune system
 * immune system cancer
 * class of disease
 * organ system cancer immune disorder
 * organ system cancer located in the immune system that is characterized by uncontrolled cellular proliferation in organs of the immune system
 * DOID:0060083
 * immune system organ benign neoplasm
 * class of disease
 * organ system benign neoplasm immune disorder
 * organ system benign neoplasm located in the immune system organs
 * DOID:0060092
 * immune-complex glomerulonephritis
 * class of disease
 * glomerulonephritis
 * Human disease
 * DOID:4784
 * immunodeficiency 11A
 * class of disease
 * autosomal recessive disease severe combined immunodeficiency
 * human disease
 * DOID:0111957
 * immunodeficiency 11B
 * class of disease
 * autosomal dominant disease T cell deficiency
 * human disease
 * DOID:0111958
 * immunodeficiency 15A
 * class of disease
 * autosomal dominant disease combined immunodeficiency severe combined immunodeficiency due to IKK2 deficiency
 * human disease
 * DOID:0111960
 * immunodeficiency 15B
 * class of disease
 * severe combined immunodeficiency autosomal recessive disease severe combined immunodeficiency due to IKK2 deficiency
 * human disease
 * DOID:0111959
 * immunodeficiency 18
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease
 * human disease
 * DOID:0111971
 * immunodeficiency 19
 * class of disease
 * autosomal recessive disease severe combined immunodeficiency
 * human disease
 * DOID:0111972
 * immunodeficiency 28
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease
 * human disease
 * DOID:0111995
 * immunodeficiency 32A
 * class of disease
 * autosomal dominant disease dendritic cell deficiency
 * human disease
 * DOID:0111986
 * immunodeficiency 32B
 * class of disease
 * monocyte, dendritic cell, and NK cell deficiency autosomal recessive disease
 * human disease
 * DOID:0111985
 * immunodeficiency 45
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
 * human disease
 * DOID:0111994
 * immunodeficiency 51
 * class of disease
 * primary immunodeficiency disease autosomal recessive disease
 * human disease
 * DOID:0111996
 * immunodeficiency 52
 * class of disease
 * T cell deficiency autosomal recessive disease
 * human disease
 * DOID:0111983
 * immunodeficiency 53
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0111992
 * immunodeficiency 55
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0111993
 * immunodeficiency 57
 * class of disease
 * autosomal recessive disease primary immunodeficiency disease
 * human disease
 * DOID:0111952
 * immunodeficiency 58
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0111984
 * immunodeficiency 59
 * class of disease
 * autosomal recessive disease B cell and dendritic cell deficiency
 * human disease
 * DOID:0111974
 * immunodeficiency 60
 * class of disease
 * combined immunodeficiency autosomal dominant disease
 * human disease
 * DOID:0111954
 * immunodeficiency 62
 * class of disease
 * autosomal recessive disease B cell deficiency
 * human disease
 * DOID:0111991
 * immunodeficiency 63
 * class of disease
 * autosomal recessive disease T cell and NK cell immunodeficiency
 * human disease
 * DOID:0111997
 * immunodeficiency 64
 * class of disease
 * T cell, B cell, and NK cell deficiency autosomal recessive disease
 * human disease
 * DOID:0111980
 * immunodeficiency 65
 * class of disease
 * primary immunodeficiency disease autosomal recessive disease
 * human disease
 * DOID:0111978
 * immunodeficiency 66
 * class of disease
 * primary immunodeficiency disease autosomal recessive disease
 * human disease
 * DOID:0111998
 * immunodeficiency 69
 * class of disease
 * autosomal recessive disease T cell and NK cell immunodeficiency
 * human disease
 * DOID:0112006
 * immunodeficiency 70
 * class of disease
 * autosomal dominant disease combined immunodeficiency
 * human disease
 * DOID:0112005
 * immunodeficiency 71
 * class of disease
 * combined immunodeficiency autosomal recessive disease
 * human disease
 * DOID:0112004
 * immunodeficiency 72
 * class of disease
 * autosomal recessive disease combined immunodeficiency
 * human disease
 * DOID:0112015
 * immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
 * class of disease
 * autosomal dominant disease combined immunodeficiency
 * human disease
 * DOID:0112061
 * immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
 * class of disease
 * combined immunodeficiency autosomal recessive disease
 * human disease
 * DOID:0112062
 * immunodeficiency-centromeric instability-facial anomalies syndrome
 * class of disease
 * autosomal recessive disease DNA repair defect other than combined T-cell and B-cell immunodeficiencies syndrome
 * autosomal recessive disease characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases
 * DOID:0090007
 * immunoglobulin A deficiency
 * class of disease
 * selective immunoglobulin deficiency disease B cell deficiency genetic disease disease
 * dysgammaglobulinemia characterized by a deficiency of immunoglobulin A
 * DOID:0060025
 * C15.378.147.333.500 C20.673.430.500
 * immunoglobulin beta deficiency
 * class of disease
 * B cell deficiency
 * Human disease
 * DOID:0060026
 * imperforate anus
 * class of disease
 * congenital disorder atresia anorectal anomalies anal disease
 * congenital disorder of digestive system
 * DOID:10488
 * C06.198.050 C16.131.314.094
 * Imperforate anus
 * Rectovestibular fistula in females.jpg
 * impulse control disorder
 * class of disease
 * mental disorder disease
 * disease of mental health that involves a failure to resist an impulsive act or behaviour that may be harmful to self or others
 * DOID:10937
 * F03.250
 * Habit and impulse disorders
 * in situ carcinoma
 * class of disease
 * pre-malignant neoplasm In situ neoplasm disease
 * human disease
 * DOID:8719
 * C04.557.470.200.240
 * Carcinomas in situ
 * In situ carcinoma-en.svg
 * inborn errors of purine–pyrimidine metabolism
 * class of disease
 * inherited metabolic disorder
 * inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism
 * DOID:653
 * C16.320.565.798 C18.452.648.798
 * inborn errors pyruvate metabolism
 * class of disease
 * carbohydrate metabolic disorder
 * human disease
 * DOID:3648
 * C16.320.565.202.810 C18.452.648.202.810
 * inborn metabolic brain disease
 * class of disease
 * metabolic brain disease
 * Human disease
 * DOID:889
 * C10.228.140.163.100 C16.320.565.189 C18.452.132.100 C18.452.648.189
 * inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
 * class of disease
 * inclusion body myopathy with Paget disease of bone and frontotemporal dementia autosomal dominant disease
 * human disease
 * DOID:0111385
 * inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
 * class of disease
 * inclusion body myopathy with Paget disease of bone and frontotemporal dementia autosomal dominant disease
 * human disease
 * DOID:0111384
 * inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
 * class of disease
 * inclusion body myopathy with Paget disease of bone and frontotemporal dementia autosomal dominant disease
 * human disease
 * DOID:0111386
 * incontinentia pigmenti achromians
 * class of disease
 * skin disease disease
 * Human disease
 * DOID:3156
 * indeterminate leprosy
 * class of disease
 * leprosy paucibacillary leprosy
 * leprosy that is an early form of the disease which causes one to a few hypopigmented or erythematous macules
 * DOID:11851
 * indolent myeloma
 * class of disease
 * smouldering myeloma multiple myeloma
 * Human disease
 * DOID:9550
 * indolent systemic mastocytosis
 * class of disease
 * mastocytoma systemic mastocytosis
 * human disease
 * DOID:4660
 * infancy electroclinical syndrome
 * class of disease
 * electroclinical syndrome epilepsy syndrome Epilepsy in children
 * electroclinical syndrome with onset in infancy occurring between birth and one year of age
 * DOID:0050703
 * infant gynecomastia
 * class of disease
 * breast disease gynecomastia
 * human disease
 * DOID:11603
 * infantile epileptic encephalopathy
 * class of disease
 * infancy electroclinical syndrome childhood onset epileptic encephalopathy West syndrome
 * Human disease
 * DOID:2481
 * C10.228.140.490.375.760 C10.228.140.490.493.875
 * infantile hypophosphatasia
 * class of disease
 * hypophosphatasia
 * A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.
 * DOID:0110914
 * infantile or early childhood epileptic encephalopathy 1
 * class of disease
 * electroclinical syndrome infantile epileptic encephalopathy
 * human disease
 * DOID:0080472
 * infantile or early childhood epileptic encephalopathy 2
 * class of disease
 * electroclinical syndrome autosomal dominant disease
 * electroclinical syndrome characterized by onset of seizures in infancy or early childhood, global developmental delay and variable intellectual disability that has material basis in heterozygous mutation in the GABRB2 gene on chromosome 5q34
 * DOID:0080471
 * infantile osteopetrosis with neuroaxonal dysplasia
 * class of disease
 * neuroaxonal dystrophy osteopetrosis
 * This syndrome is characterized by osteopetrosis, agenesis of the corpus callosum, cerebral atrophy and a small hippocampus
 * DOID:0070343
 * infantile-onset distal myopathy
 * class of disease
 * distal muscular dystrophy
 * distal muscular dystrophy characterized by autosomal dominant inheritance, infantile onset and progressive disease development
 * DOID:0070196
 * infected hydrocele
 * class of disease
 * hydrocele
 * Human disease
 * DOID:9911
 * infectious disease
 * class of disease
 * disease infection associated with diseases
 * disease caused by infection of pathogenic biological agents in a host organism
 * DOID:0050117
 * C01.539.221
 * Infectious diseases and disorders
 * Malaria.jpg
 * infective endocarditis
 * class of disease
 * endocarditis cardiovascular Infection infectious disease disease
 * endocarditis that is characterized by inflammation of the endocardium caused by infectious agents.
 * DOID:0060000
 * Haemophilus parainfluenzae Endocarditis PHIL 851 lores.jpg
 * infective urethral stricture
 * class of disease
 * urethral stricture
 * Human disease
 * DOID:13658
 * inferior myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5850
 * C14.280.647.500.187 C14.907.585.500.187 C23.550.513.355.750.187 C23.550.717.489.750.187
 * inferolateral myocardial infarct
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5852
 * infertility
 * class of disease symptom or sign
 * reproductive system disease reproductive system symptom disease
 * inability of a person, animal or plant to reproduce by natural means that is no intervention of contraceptive techniques
 * DOID:5223
 * C12.294.365 C13.351.500.365
 * Infertility
 * Infertility causes.png
 * infertility due to extratesticular cause
 * class of disease
 * male infertility
 * Human disease
 * DOID:14096
 * infiltrating angiolipoma
 * class of disease
 * angiolipoma
 * Human disease
 * DOID:3615
 * infiltrating bladder lymphoepithelioma-like carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * human disease
 * DOID:7600
 * infiltrating bladder urothelial carcinoma sarcomatoid variant
 * class of disease
 * invasive bladder transitional cell carcinoma sarcomatoid transitional cell carcinoma
 * Human disease
 * DOID:7553
 * infiltrating lipoma
 * class of disease
 * lipoma
 * Human disease
 * DOID:7014
 * infiltrating nipple syringomatous adenoma
 * class of disease
 * nipple neoplasm
 * Human disease
 * DOID:7839
 * infiltrating renal pelvis transitional cell carcinoma
 * class of disease
 * renal pelvis transitional cell carcinoma
 * Human disease
 * DOID:0050620
 * infiltrating ureter transitional cell carcinoma
 * class of disease
 * ureter transitional cell carcinoma
 * Human disease
 * DOID:6845
 * infiltrative basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4299
 * inflamed seborrheic keratosis
 * class of disease
 * seborrheic keratosis
 * Human disease
 * DOID:11685
 * inflammatory MFH
 * class of disease
 * malignant fibrous histiocytoma
 * Human disease
 * DOID:6192
 * inflammatory and toxic neuropathy
 * class of disease
 * peripheral neuropathy acquired peripheral neuropathy
 * Human disease
 * DOID:2537
 * inflammatory bowel disease 1
 * class of disease
 * inflammatory bowel diseases genetic disease
 * An inflammatory bowel disease that has material basis in mutations in the NOD2 gene on chromosome 16q12.1.
 * DOID:0110892
 * inflammatory bowel disease 11
 * class of disease
 * inflammatory bowel diseases genetic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 7q22
 * DOID:0110894
 * inflammatory bowel disease 12
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 3p21.3
 * DOID:0110887
 * inflammatory bowel disease 13
 * class of disease
 * inflammatory bowel diseases genetic disease
 * An inflammatory bowel disease that has material basis in variation in the ABCB1 gene on chromosome 7q21.1.
 * DOID:0110893
 * inflammatory bowel disease 15
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 10q21
 * DOID:0110897
 * inflammatory bowel disease 16
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 9q32
 * DOID:0110896
 * inflammatory bowel disease 17
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the IL23R gene on chromosome 1p31.3.
 * DOID:0110883
 * inflammatory bowel disease 18
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 5p13.1.
 * DOID:0110888
 * inflammatory bowel disease 2
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 12p13.2-q24.1.
 * DOID:0110900
 * inflammatory bowel disease 20
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 10q23-q24
 * DOID:0110898
 * inflammatory bowel disease 21
 * class of disease
 * inflammatory bowel diseases genetic disease autosomal dominant disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 18p11
 * DOID:0110906
 * inflammatory bowel disease 22
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 17q21.2.
 * DOID:0110905
 * inflammatory bowel disease 23
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 1q32.1.
 * DOID:0110884
 * inflammatory bowel disease 24
 * class of disease
 * inflammatory bowel diseases genetic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome 20q13
 * DOID:0110908
 * inflammatory bowel disease 26
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 12q15
 * DOID:0110901
 * inflammatory bowel disease 27
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 13q13.3
 * DOID:0110902
 * inflammatory bowel disease 3
 * class of disease
 * inflammatory bowel diseases genetic disease autosomal dominant disease
 * An inflammatory bowel disease that has material basis in variation in the chromosome region 6p21.3.
 * DOID:0110891
 * inflammatory bowel disease 4
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 14q11-q12
 * DOID:0110903
 * inflammatory bowel disease 5
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 5q31
 * DOID:0110889
 * inflammatory bowel disease 6
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 19p13
 * DOID:0110907
 * inflammatory bowel disease 7
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 1p36
 * DOID:0110882
 * inflammatory bowel disease 8
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 16p
 * DOID:0110904
 * inflammatory bowel disease 9
 * class of disease
 * inflammatory bowel diseases genetic disease monogenic disease
 * inflammatory bowel disease that has material basis in variation in the chromosome region 3p26
 * DOID:0110886
 * inflammatory bowel diseases
 * class of disease
 * intestinal disease immune disorder disease
 * intestinal disease characterized by inflammation located in all parts of digestive tract
 * DOID:0050589
 * C06.405.205.731 C06.405.469.432
 * Inflammatory bowel diseases
 * Cryptitis high mag.jpg
 * inflammatory breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:6263
 * inflammatory diarrhea
 * class of disease
 * diarrhea mucositis
 * Human disease
 * DOID:0050132
 * inflammatory leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5251
 * inflammatory liposarcoma
 * class of disease
 * atypical lipomatous tumor
 * Human disease
 * DOID:8233
 * inflammatory myofibroblastic tumour
 * class of disease
 * mesenchymal cell neoplasm connective tissue benign neoplasm
 * mesenchymal cell neoplasm that has material basis in myofibroblastic cells admixed with inflammatory cells
 * DOID:0050905
 * Inflammatory myofibroblastic tumour
 * inflammatory spondylopathy
 * class of disease
 * spondylitis
 * Human disease
 * DOID:12105
 * infratentorial cancer
 * class of disease
 * brain cancer infratentorial neoplasm
 * brain cancer that is located in the infratentorial region
 * DOID:4706
 * infundibulocystic basal cell carcinoma
 * class of disease
 * basal-cell carcinoma inherited skin tumor
 * Human disease
 * DOID:4279
 * inguinal hernia
 * class of disease
 * intestinal disease disease
 * intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal
 * DOID:0060320
 * C23.300.707.374.875
 * Inguinal hernia
 * Inguinalhernia.gif
 * inherited metabolic disorder
 * class of disease
 * genetic disease rare disease metabolic disease disease
 * class of disease including endocrine diseases, nutritional diseases and metabolic diseases
 * DOID:655
 * C16.320.565 C18.452.648
 * Inborn errors of metabolism
 * inhibited female orgasm
 * class of disease
 * female reproductive system disease anorgasmia female orgasm
 * Human disease
 * DOID:7518 DOID:11110
 * inner ear cancer
 * class of disease
 * auricular cancer inner ear neoplasm
 * Human disease
 * DOID:5102
 * inner ear disease
 * class of disease
 * ear disease
 * human disease
 * DOID:2952 DOID:4539
 * C09.218.568
 * insulinoma
 * class of disease
 * pancreatic cystadenoma benign neoplasms by histologic type islet cell adenoma disease
 * tumor that produces too much insulin
 * DOID:3892
 * C04.557.470.035.100.852 C04.588.274.761.249.500 C04.588.322.475.249.500 C06.301.761.249.500 C06.689.667.249.500 C19.344.421.249.500
 * Insulinoma
 * Pancreatic insulinoma (2).JPG
 * integrative agnosia
 * class of disease
 * agnosia apperceptive agnosia
 * agnosia that is a loss of the ability to integrate these elements together into comprehensible perceptual wholes while recognizing elements of the whole
 * DOID:0060143
 * integumentary system benign neoplasm
 * class of disease
 * organ system benign neoplasm integumentary system neoplasm
 * organ system benign neoplasm located in the integumentary system organs
 * DOID:0060121
 * integumentary system cancer
 * class of disease
 * organ system cancer integumentary system neoplasm integumentary system disease
 * organ system cancer that is located in the skin, hair and nails
 * DOID:0060122
 * integumentary system disease
 * class of disease
 * disease of anatomical entity
 * disease of anatomical entity that is located in the integumentary system comprising the skin and its appendages
 * DOID:16
 * intellectual developmental disorder with short stature and behavioral abnormalities
 * class of disease
 * syndrome autosomal recessive disease syndromic intellectual disability
 * human disease
 * DOID:0111674
 * intellectual disability
 * class of disease
 * specific developmental disorder cognitive deficit disability disease
 * generalized neurodevelopmental disorder
 * DOID:1059
 * C23.888.592.604.646 C10.597.606.360 F01.700.687 F03.625.539
 * Intellectual disabilities
 * interdigitating dendritic cell sarcoma
 * class of disease
 * histiocytic and dendritic cell cancer dendritic cell sarcoma
 * histiocytic and dendritic cell cancer that effect dendritic cells
 * DOID:7848
 * C04.557.227.199 C15.604.250.390.199
 * interleukin-7 receptor alpha deficiency
 * class of disease
 * severe combined immunodeficiency
 * human disease
 * DOID:0060015
 * intermediate malignant teratoma
 * class of disease
 * immature teratoma
 * Human disease
 * DOID:7202
 * intermediate uveitis
 * class of disease
 * uveitis
 * human disease
 * DOID:12732
 * C11.941.879.900
 * Intermediate uveitis
 * intermittent asthma
 * class of disease
 * chronic asthma
 * human disease
 * DOID:0080812
 * intermittent explosive disorder
 * class of disease
 * impulse control disorder disease
 * Mood disorder identified by frequent episodes of anger and rage
 * DOID:12401
 * intermittent proptosis
 * class of disease
 * orbital disease exophthalmos
 * Human disease
 * DOID:12363
 * intermittent squint
 * class of disease
 * strabismus
 * Human disease
 * DOID:1942
 * intermixed schwannian stroma-rich ganglioneuroblastoma
 * class of disease
 * ganglioneuroblastoma
 * Human disease
 * DOID:5194
 * internal hemorrhoid
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9749
 * internal resorption
 * class of disease
 * tooth resorption
 * human disease
 * DOID:13239
 * internuclear ophthalmoplegia
 * class of disease
 * ophthalmoplegia strabismus
 * Human disease
 * DOID:538
 * Internuclear ophthalmoplegia.jpg
 * interstitial keratitis
 * class of disease
 * connective tissue disease deep keratitis
 * human disease
 * DOID:9857
 * interstitial myocarditis
 * class of disease
 * mediastinitis myocarditis
 * Inflammation of the heart characterized by infiltration of the interstitial tissues by inflammatory cells, histiocytes, and the formation of granulomas. Giant cells are often present.
 * DOID:817
 * interstitial nephritis
 * class of disease
 * nephritis kidney disease disease
 * type of nephritis affecting the interstitium of the kidneys surrounding the tubules
 * DOID:1063
 * C12.200.777.419.570.643 C12.050.351.968.419.570.643 C12.950.419.570.643
 * Tubulointerstitial disease
 * interval angle-closure glaucoma
 * class of disease
 * primary angle-closure glaucoma
 * Human disease
 * DOID:13549
 * intestinal atresia
 * class of disease
 * intestinal disease intestinal malformation
 * congenital disorder of digestive system
 * DOID:10486
 * C06.198.719 C06.405.469.445 C16.131.314.466
 * Intestinal atresia
 * DuodAtres.png
 * intestinal benign neoplasm
 * class of disease
 * gastrointestinal system benign neoplasm intestinal neoplasm intestinal disease
 * gastrointestinal system benign neoplasm that is located in the intestine
 * DOID:4610
 * intestinal cancer
 * class of disease
 * gastrointestinal system cancer intestinal neoplasm intestinal disease
 * gastrointestinal system cancer that is located in the intestine
 * DOID:10155
 * Intestinal cancers
 * intestinal disaccharidase deficiency
 * class of disease
 * metabolic disease with intestinal involvement intestinal disease carbohydrate metabolic disorder
 * Human disease
 * DOID:9868
 * intestinal disease
 * class of disease
 * gastrointestinal system disease
 * gastrointestinal system disease that is located in the intestine
 * DOID:5295
 * C06.405.469
 * Diseases and disorders of intestines
 * intestinal impaction
 * class of disease
 * bowel obstruction
 * Human disease
 * DOID:8448
 * intestinal neuroendocrine benign tumor
 * class of disease
 * intestinal benign neoplasm gastrointestinal neuroendocrine benign tumor
 * Human disease
 * DOID:4119
 * intestinal perforation
 * class of disease
 * intestinal disease gastrointestinal perforation
 * Human disease
 * DOID:2074
 * C06.405.469.557
 * intestinal tuberculosis
 * class of disease
 * gastrointestinal tuberculosis intestinal disease
 * human disease
 * DOID:13282
 * intestinal variant cervical mucinous adenocarcinoma
 * class of disease
 * cervical mucinous adenocarcinoma intestinal type carcinoma
 * Human disease
 * DOID:8339
 * intestinal volvulus
 * class of disease
 * bowel obstruction disease
 * Human disease
 * DOID:8445
 * C06.405.469.531.568 C23.300.970.500
 * Volvulus
 * intestine carcinoma in situ
 * class of disease
 * carcinoma in situ of digestive organ in situ carcinoma intestinal disease
 * Human disease
 * DOID:9024
 * intra-abdominal lymph node mast cell malignancy
 * class of disease
 * lymph node cancer mast cell malignancy of lymph nodes mastocytoma
 * Human disease
 * DOID:13005
 * intracerebral cystic meningioma
 * class of disease
 * cerebral meningioma
 * Human disease
 * DOID:6113
 * intracortical osteogenic sarcoma
 * class of disease
 * conventional central osteosarcoma
 * Human disease
 * DOID:7602
 * intracranial abscess
 * class of disease
 * central nervous system disease abscess
 * central nervous system disease that is located in the skull and is characterized by a collection of pus (infected material) inside the skull
 * DOID:10095
 * intracranial aneurysm
 * class of disease
 * aneurysm cerebrovascular disease cerebral arterial disease disease
 * cerebrovascular disorder
 * DOID:10941
 * C10.228.140.300.510.600 C14.907.055.635 C14.907.253.560.300
 * Cerebral aneurysms
 * Aneurysem.jpg
 * intracranial arterial disease
 * class of disease
 * cerebrovascular disease
 * human disease
 * DOID:13089
 * C10.228.140.300.510 C14.907.253.560
 * intracranial arteriosclerosis
 * class of disease
 * arteriosclerosis
 * human disease
 * DOID:13097
 * C10.228.140.300.510.800 C14.907.137.126.372 C14.907.253.560.350
 * intracranial berry aneurysm
 * class of disease
 * intracranial aneurysm
 * intracranial aneurysm with a characteristic rounded shape; the most common form of cerebral aneurysm
 * DOID:0060228
 * intracranial berry aneurysm 11
 * class of disease
 * intracranial berry aneurysm
 * human disease
 * DOID:0080974
 * intracranial berry aneurysm 9
 * class of disease
 * intracranial berry aneurysm
 * human disease
 * DOID:0080972
 * intracranial cavernous angioma
 * class of disease
 * intracranial structure hemangioma
 * Human disease
 * DOID:2516
 * intracranial chondrosarcoma
 * class of disease
 * extraosseous chondrosarcoma extraskeletal myxoid chondrosarcoma intracranial tumor
 * Human disease
 * DOID:7903
 * intracranial embolism
 * class of disease
 * cerebrovascular disease disease
 * Human disease
 * DOID:4372
 * C10.228.140.300.525.400 C14.907.253.566.300 C14.907.355.590.213.300
 * Intracranial embolism
 * intracranial liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5714
 * intracranial primitive neuroectodermal tumor
 * class of disease
 * central nervous system primitive neuroectodermal neoplasm medulloblastoma
 * Human disease
 * DOID:4788
 * intracranial structure hemangioma
 * class of disease
 * hemangioma intracranial tumor
 * Human disease
 * DOID:2517
 * intracranial thrombosis
 * class of disease
 * thrombosis cerebrovascular disease thromboembolism
 * Human disease
 * DOID:4193
 * C10.228.140.300.525.425 C14.907.253.566.350 C14.907.355.590.213.350
 * intracranial vasospasm
 * class of disease
 * vasospasm cerebrovascular disease disease
 * Human disease
 * DOID:13100
 * C10.228.140.300.900 C14.907.253.951
 * intracystic papillary adenoma
 * class of disease
 * adenoma
 * Human disease
 * DOID:2682
 * intraductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:8068
 * intraductal breast neoplasm
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:3013
 * intraductal carcinoma
 * class of disease
 * breast carcinoma in situ breast ductal carcinoma disease
 * Human disease
 * DOID:0060074
 * C04.557.470.200.025.275 C04.557.470.200.240.187.250 C04.557.470.615.275
 * Ductal carcinoma in situ
 * Breast DCIS histopathology (1).jpg
 * intraductal papillary breast neoplasm
 * class of disease
 * intraductal breast neoplasm
 * Human disease
 * DOID:1628
 * intraductal papilloma
 * class of disease
 * breast benign neoplasm papilloma intraductal breast neoplasm disease
 * human disease
 * DOID:1627
 * C04.557.470.615.670
 * Intraductal papilloma
 * intrahepatic bile duct adenoma
 * class of disease
 * bile duct adenoma
 * Human disease
 * DOID:5437
 * intrahepatic bile duct cystadenoma
 * class of disease
 * bile duct cystadenoma intrahepatic bile duct adenoma
 * Human disease
 * DOID:6733
 * intrahepatic biliary papillomatosis
 * class of disease
 * biliary papillomatosis
 * Human disease
 * DOID:8230
 * intrahepatic cholangiocarcinoma
 * class of disease
 * cholangiocarcinoma
 * Human disease
 * DOID:4928
 * intrahepatic cholestasis
 * class of disease
 * cholestasis
 * medical condition
 * DOID:1852
 * C06.130.120.135.250 C06.552.150
 * intrahepatic cholestasis of pregnancy
 * class of disease
 * intrahepatic cholestasis liver disease of pregnancy disease
 * intrahepatic cholestasis characterized by reversible cholestasis typically occurring in the second or third trimester of pregnancy, elevated serum aminotransferases and bile acid level and resolution of symptoms by 2 to 3 weeks after delivery
 * DOID:0070227
 * Cholestasis high mag.jpg
 * intrahepatic gall duct cancer
 * class of disease
 * gallbladder cancer
 * Human disease
 * DOID:12298
 * intramuscular hemangioma
 * class of disease
 * hemangioma muscle neoplasm
 * Human disease
 * DOID:468
 * intraneural perineurioma
 * class of disease
 * perineurioma
 * Human disease
 * DOID:4696
 * intraocular lymphoma
 * class of disease
 * eye lymphoma
 * human disease
 * DOID:775
 * C04.557.386.435 C04.588.364.447 C15.604.515.569.417 C20.683.515.761.417
 * intraorbital meningioma
 * class of disease
 * orbital cancer meningioma
 * meningioma by site and orbital neoplasm that is located in the area around the eye sockets of the skull and results in pressure in the eyes, giving a bulging appearance
 * DOID:4141
 * intrapelvic lymph node leukemic reticuloendotheliosis
 * class of disease
 * lymph node cancer
 * Human disease
 * DOID:12972
 * intratubular embryonal carcinoma
 * class of disease
 * embryonal testis carcinoma
 * embryonal testis carcinoma that is located within a tubule
 * DOID:8275
 * intravascular angioleiomyoma
 * class of disease
 * angiomyoma vascular neoplasm
 * Human disease
 * DOID:4266
 * intravascular fasciitis
 * class of disease
 * pseudosarcomatous fibromatosis
 * Human disease
 * DOID:9603
 * intravenous leiomyomatosis
 * class of disease
 * leiomyomatosis vascular disease
 * Human disease
 * DOID:5729
 * intraventricular meningioma
 * class of disease
 * cerebral ventricle cancer meningioma
 * Human disease
 * DOID:3772
 * intrinsic asthma
 * class of disease
 * asthma chronic asthma
 * human disease
 * DOID:9360
 * intussusception
 * class of disease
 * bowel obstruction genetic disease disease
 * human disease
 * DOID:8446
 * C06.405.469.531.577
 * Intussusception
 * VolvulusCT.PNG
 * invasive bladder transitional cell carcinoma
 * class of disease
 * bladder urothelial carcinoma Invasive urothelial carcinoma
 * Human disease
 * DOID:6477
 * invasive lobular carcinoma
 * class of disease
 * breast lobular carcinoma invasive breast carcinoma carcinoma breast cancer disease
 * Human disease
 * DOID:3457
 * Histopathology of invasive lobular carcinoma (ILC)
 * invasive malignant thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:3283
 * invasive tubular breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive ductal carcinoma
 * Human disease
 * DOID:6587
 * inverted follicular keratosis
 * class of disease
 * seborrheic keratosis
 * Human disease
 * DOID:6945
 * Inverted follicular keratosis
 * inverted papilloma
 * class of disease
 * papilloma
 * Human disease
 * DOID:3179
 * C04.557.470.700.600.610
 * Inverted papillomas
 * inverted transitional papilloma
 * class of disease
 * transitional papilloma inverted papilloma
 * Human disease
 * DOID:4630
 * iodine hypothyroidism
 * class of disease
 * hypothyroidism
 * Human disease
 * DOID:5083
 * iris cancer
 * class of disease
 * iris neoplasm uveal cancer iris disease
 * Human disease
 * DOID:3478
 * iris disease
 * class of disease
 * uveal disease
 * Human disease
 * DOID:240 DOID:4738
 * C11.941.375
 * iritis
 * class of disease
 * iris disease anterior uveitis disease
 * human disease
 * DOID:1406
 * C11.941.375.385 C11.941.879.780.880.448
 * iron deficiency anemia
 * class of disease symptom or sign
 * deficiency anemia nutritional deficiency disease iron deficiency hypochromic anemia disease
 * anemia caused by a lack of iron
 * DOID:11758
 * C15.378.071.196.300 C18.452.565.100
 * Iron-deficiency anemia
 * Heme b.svg
 * iron metabolism disease
 * class of disease
 * mineral metabolism disease
 * Human disease
 * DOID:2351
 * C18.452.565
 * irregular astigmatism
 * class of disease
 * astigmatism
 * Human disease
 * DOID:13919
 * irritable bowel syndrome
 * class of disease symptom or sign
 * functional colonic disease syndrome intestinal disease disease
 * syndrome that is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause
 * DOID:9778
 * C06.405.469.158.272.608
 * Irritable bowel syndrome
 * Irritable bowel syndrome.jpg
 * irritant dermatitis
 * class of disease
 * contact dermatitis
 * human disease
 * DOID:2772
 * C17.800.174.255.400 C17.800.815.255.400
 * Irritant contact dermatitis
 * ischemic bone disease
 * class of disease
 * bone disease ischemia
 * bone disease that results in an interruption of blood supply located in bone
 * DOID:0080008
 * ischemic colitis
 * class of disease
 * colitis
 * colitis caused by inadequate blood supply to the colon
 * DOID:0060181
 * C06.405.205.265.115 C06.405.469.158.188.115 C14.907.286
 * Ischemic colitis
 * ischemic fasciitis
 * class of disease
 * fasciitis
 * human disease
 * DOID:9601
 * Ischemic fasciitis
 * ischemic neuropathy
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:1195
 * islet cell carcinoma
 * class of disease
 * islet cell tumor gastrointestinal carcinoma disease
 * islet cell tumor that has material basis in epithelial cells
 * DOID:1798
 * C04.557.470.200.025.290 C04.588.274.761.500 C04.588.322.475.500 C06.301.761.500 C06.689.667.500 C19.344.421.500
 * Pancreatic neuroendocrine tumors
 * islet cell tumor
 * class of disease
 * pancreatic cancer
 * pancreatic cancer that is located in the pancreatic islet cells
 * DOID:1799
 * isocyanates allergic asthma
 * class of disease
 * allergic asthma occupational asthma
 * allergic asthma that has allergic trigger isocyanates
 * DOID:0040041
 * isolated cryptophthalmia
 * class of disease
 * cryptophthalmos
 * human disease
 * DOID:0111717
 * isolated ectopia lentis
 * class of disease
 * lens disease ectopia lentis
 * A lens disease characterized by abnormal stretching of the zonular fibers resulting in dislocation of the lens. This dislocation may be mild to severe and may progress with age.
 * DOID:0111148
 * isolated growth hormone deficiency type IA
 * class of disease
 * isolated growth hormone deficiency
 * human disease
 * DOID:0060873
 * isolated growth hormone deficiency type IB
 * class of disease
 * isolated growth hormone deficiency
 * human disease
 * DOID:0060874
 * isolated growth hormone deficiency type II
 * class of disease
 * isolated growth hormone deficiency
 * human disease
 * DOID:0060872
 * isolated growth hormone deficiency type III
 * class of disease
 * isolated growth hormone deficiency X-linked recessive disease
 * An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material basis in mutation in the BTK gene on chromosome Xq22.1.
 * DOID:0060875
 * isolated microphthalmia
 * class of disease
 * microphthalmia
 * microphthalmia that is not part of a larger syndrome
 * DOID:0080637
 * isolated microphthalmia 1
 * class of disease
 * microphthalmia genetic disease isolated microphthalmia autosomal recessive disease
 * microphthalmia that has material basis in variation in the chromosomal region 14q32
 * DOID:0060840
 * isoniazide allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger isoniazide
 * DOID:0040008
 * isthmicoma
 * class of disease
 * hair follicle neoplasm
 * Human disease
 * DOID:8426
 * Isthmicoma
 * isthmus cancer
 * class of disease
 * uterine corpus cancer
 * Human disease
 * DOID:9459
 * jaw cancer
 * class of disease
 * bone cancer neoplasm of jaw
 * bone cancer and jaw disease that is located in the jaw and results in a swollen jaw, results in numbness or a tingling sensation in jaw, and results in an abnormal growth of the jaw bone
 * DOID:1862
 * jaw-winking syndrome
 * class of disease
 * cranial nerve disease ptosis genetic peripheral neuropathy
 * autosomal dominant condition with incomplete penetrance, in which nursing infants will have rhythmic upward jerking of their upper eyelid
 * DOID:560
 * Marcus Gunn phenomenon
 * jejunal adenocarcinoma
 * class of disease
 * jejunal cancer adenocarcinoma
 * jejunal cancer that is located in the jejunum and has material basis in epithelial tissue that has glandular origin
 * DOID:0050926
 * jejunal cancer
 * class of disease
 * small intestine cancer jejunal neoplasm
 * human disease
 * DOID:13499
 * jejunal neoplasm
 * class of disease
 * small intestine neoplasm jejunal disease
 * human disease
 * DOID:3218
 * C04.588.274.476.411.523 C06.301.371.411.523 C06.405.249.411.523 C06.405.469.491.523 C06.405.469.600.523
 * jejunal somatostatinoma
 * class of disease
 * jejunal cancer
 * Human disease
 * DOID:3216
 * junctional epidermolysis bullosa Herlitz type
 * class of disease
 * junctional epidermolysis bullosa genetic disease autosomal recessive disease
 * Human disease
 * DOID:0060737
 * juvenile absence epilepsy
 * class of disease
 * adolescence-adult electroclinical syndrome
 * adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures
 * DOID:0060172
 * juvenile absence epilepsy 1
 * class of disease
 * juvenile absence epilepsy
 * human disease
 * DOID:0111324
 * juvenile amyotrophic lateral sclerosis with dementia
 * class of disease
 * amyotrophic lateral sclerosis juvenile amyotrophic lateral sclerosis
 * juvenile amyotrophic lateral sclerosis that is slowly progressive with concomitantly progressive dementia
 * DOID:0110067
 * juvenile ankylosing spondylitis
 * class of disease
 * autoimmune disease of musculoskeletal system ankylosing spondylitis
 * autoimmune disease of musculoskeletal system that is an ankylosing spondylitis with onset during childhood
 * DOID:0040092
 * juvenile astrocytoma
 * class of disease
 * astrocytoma childhood cancer
 * Human disease
 * DOID:3079
 * juvenile dermatitis herpetiformis
 * class of disease
 * dermatitis herpetiformis
 * Human disease
 * DOID:8507
 * juvenile glaucoma
 * class of disease
 * autosomal dominant disease primary open angle glaucoma
 * Human disease
 * DOID:1068
 * juvenile myelomonocytic leukemia
 * class of disease
 * myelodysplastic/myeloproliferative neoplasm monocytic leukemia childhood leukemia
 * Human disease
 * DOID:0050458
 * C04.557.337.539.525 C15.378.190.615.520
 * juvenile myoclonic epilepsy
 * class of disease
 * adolescence-adult electroclinical syndrome Idiopathic generalized epilepsy myoclonic epilepsy
 * adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years
 * DOID:4890
 * C10.228.140.490.493.063.670 C10.228.140.490.375.130.670
 * juvenile myoclonic epilepsy 10
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111325
 * juvenile myoclonic epilepsy 3
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111326
 * juvenile myoclonic epilepsy 4
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111327
 * juvenile myoclonic epilepsy 9
 * class of disease
 * juvenile myoclonic epilepsy
 * human disease
 * DOID:0111328
 * juvenile pilocytic astrocytoma
 * class of disease
 * childhood pilocytic astrocytoma pilocytic astrocytoma
 * Human disease
 * DOID:6811
 * juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
 * class of disease
 * autosomal dominant disease syndrome juvenile polyposis syndrome hereditary hemorrhagic telangiectasia
 * human disease
 * DOID:0111543
 * juvenile type testicular granulosa cell tumor
 * class of disease
 * testicular granulosa cell tumor
 * Human disease
 * DOID:6032
 * juvenile xanthogranuloma
 * class of disease
 * non-Langerhans-cell histiocytosis histiocytosis xanthogranuloma
 * Human disease
 * DOID:4424
 * C15.604.250.410.900 C17.800.973
 * Juvenile xanthogranuloma
 * juvenile-onset Parkinson disease
 * class of disease
 * Parkinson's disease young-onset Parkinson disease
 * human disease
 * DOID:0060893
 * juxtacortical chondroma
 * class of disease
 * chondroma
 * Human disease
 * DOID:2601
 * juxtacortical chondrosarcoma
 * class of disease
 * chondrosarcoma
 * human disease
 * DOID:5866
 * juxtacortical osteosarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:3373
 * C04.557.450.565.575.650.655 C04.557.450.795.620.655
 * keratinizing squamous cell carcinoma
 * class of disease
 * squamous cell carcinoma
 * squamous cell carcinoma that presents as single, isolated cells with bizzare cytoplasmic shapes, intense cytoplasmic eosinophilia, and intensely hyperchromatic, angular nuclei in a background of necrotic and keratinous debris
 * DOID:5521
 * keratitis
 * class of disease symptom or sign
 * corneal disease eye inflammation inflammatory disease cornea symptom disease
 * corneal disease that is characterized by inflammation of the cornea.
 * DOID:4677
 * C11.204.564
 * Keratitis
 * Clare-314.jpg
 * keratoacanthoma
 * class of disease
 * cutaneous squamous-cell carcinoma disease
 * Human disease
 * DOID:3149
 * C17.800.417
 * Keratoacanthoma
 * Keratoacanthoma 2.jpg
 * keratoconjunctivitis
 * class of disease
 * keratitis conjunctivitis eye disease
 * inflammation ("-itis") of the cornea and conjunctiva.
 * DOID:9368
 * C11.187.183.394 C11.204.564.585
 * Keratoconjunctivitis
 * Gade corneyo-djontivite clamidia3.jpg
 * keratoconjunctivitis sicca
 * class of disease
 * dry eye syndrome keratoconjunctivitis disease
 * condition of having dry eyes
 * DOID:12895
 * C11.187.183.394.550 C11.204.564.585.630 C11.496.260.394
 * Dry eye syndrome
 * keratomalacia
 * class of disease
 * corneal degeneration vitamin A deficiency keratitis related to vitamin deficiency disease
 * Human disease
 * DOID:11267
 * keratopathy
 * class of disease
 * corneal disease
 * Human disease
 * DOID:2283
 * keratosis
 * class of disease
 * skin disease keratoma disease
 * skin disease characterized by growth of keratin on the skin or mucous membranes
 * DOID:161
 * C17.800.428
 * Keratosis pilaris arm.jpg
 * keratosis follicularis spinulosa decalvans, autosomal dominant
 * class of disease
 * keratosis follicularis spinulosa decalvans
 * human disease
 * DOID:0080755
 * keratosis pilaris atrophicans faciei
 * class of disease
 * keratosis pilaris atropicans
 * human disease
 * DOID:0080752
 * keratosis pilaris atropicans
 * class of disease
 * keratosis pilaris autosomal recessive disease ichthyosis
 * human disease
 * DOID:0080751
 * kernicterus
 * class of disease symptom or sign
 * encephalopathy neurometabolic disease neonatal jaundice disease
 * congenital disorder of nervous system
 * DOID:2382
 * C10.228.140.163.480 C15.378.295.502 C16.614.304.502 C18.452.132.480 C20.306.502 C23.550.429.750
 * Kernicterus
 * kernicterus due to isoimmunization
 * class of disease
 * neonatal jaundice kernicterus
 * Human disease
 * DOID:12043
 * ketoprofen photoallergic dermatitis
 * class of disease
 * photodermatitis drug allergy
 * photoallergic dermatitis that has allergic trigger ketoprofen
 * DOID:0040060
 * kidney angiomyolipoma
 * class of disease
 * kidney benign neoplasm angiomyolipoma benign perivascular tumor
 * angiomyolipoma arising from the kidney
 * DOID:8411
 * Renal angiomyolipoma
 * kidney benign neoplasm
 * class of disease
 * urinary system benign neoplasm kidney neoplasm kidney disease lipoma
 * A non-metastasizing neoplasm that arises from the kidney. Representative examples include cystic nephroma, metanephric adenoma, oncocytoma, and urothelial papilloma of the renal pelvis.
 * DOID:3116
 * kidney cancer
 * class of disease
 * urinary system cancer kidney neoplasm kidney disease disease
 * urinary system cancer that is located in the kidney
 * DOID:263
 * Cancers of kidney
 * kidney carcinoma in situ
 * class of disease
 * kidney disease in situ carcinoma
 * Human disease
 * DOID:9234
 * kidney clear cell sarcoma
 * class of disease
 * kidney cancer kidney sarcoma inherited renal tumor clear-cell sarcoma
 * kidney sarcoma that has material basis in clear cells that are characterized as cells that look clear when viewed under a microscope
 * DOID:4880
 * kidney cortex disease
 * class of disease
 * kidney disease
 * human disease
 * DOID:0080616
 * kidney failure
 * class of disease symptom or sign
 * kidney disease impaired renal function disease chronic renal disease urological symptom disease
 * disease where the kidneys fail to adequately filter waste products from the blood
 * DOID:1074
 * C12.777.419.780 C13.351.968.419.780
 * kidney fibrosarcoma
 * class of disease
 * kidney sarcoma fibrosarcoma
 * Human disease
 * DOID:5982
 * kidney hemangiopericytoma
 * class of disease
 * kidney cancer
 * kidney cancer which is manifested in the kidney
 * DOID:262
 * kidney hypertrophy
 * class of disease
 * kidney disease
 * Global enlargement of the renal parenchyma in one or both kidneys
 * DOID:9622
 * kidney infection
 * class of disease
 * infection kidney disease infectious disease
 * type of infection that afflicts the kidneys
 * DOID:782
 * kidney leiomyosarcoma
 * class of disease
 * kidney sarcoma
 * leiomyosarcoma and sarcoma of kidney that is located in the kidney
 * DOID:5287
 * kidney lipoma
 * class of disease
 * kidney benign neoplasm
 * Human disease
 * DOID:10194
 * kidney liposarcoma
 * class of disease
 * liposarcoma kidney sarcoma kidney cancer
 * liposarcoma that is located in the kidney
 * DOID:5699
 * kidney osteogenic sarcoma
 * class of disease
 * kidney sarcoma extraosseous osteosarcoma
 * kidney sarcoma that starts in the bones and that is located in the kidney
 * DOID:5983
 * kidney papillary necrosis
 * class of disease
 * kidney disease disease
 * Human disease
 * DOID:2981
 * C12.777.419.493 C13.351.968.419.493
 * kidney pelvis papillary carcinoma
 * class of disease
 * renal pelvis transitional cell carcinoma renal pelvis papillary tumor papillary transitional carcinoma
 * Human disease
 * DOID:5973
 * kidney pelvis sarcomatoid transitional cell carcinoma
 * class of disease
 * sarcomatoid transitional cell carcinoma transitional cell carcinoma renal pelvis carcinoma
 * Human disease
 * DOID:6844
 * kidney rhabdoid cancer
 * class of disease
 * rhabdoid tumor kidney sarcoma
 * embryonal cancer that is located in the kidney
 * DOID:3674
 * kidney sarcoma
 * class of disease
 * kidney cancer sarcoma
 * kidney cancer that is located in the kidney&#39;s connective tissue
 * DOID:4242
 * klebsiellosis
 * class of disease
 * bacterial pneumonia Enterobacteriaceae infectious disease
 * infection by Klebsiella bacteria
 * DOID:13272
 * C01.150.252.400.310.503
 * kleptomania
 * class of disease
 * impulse control disorder disease
 * inability to resist the urge to steal
 * DOID:12400
 * Kleptomania
 * Constant Wauters Der ertappte Hausdiener.jpg
 * kwashiorkor
 * class of disease
 * protein-energy malnutrition disease dystrophy protein deficiency
 * Human disease
 * DOID:13579
 * C18.654.521.719.500
 * Kwashiorkor
 * Kwashiorkor 6180.jpg
 * kyphoscoliotic heart disease
 * class of disease
 * chronic pulmonary heart disease
 * Human disease
 * DOID:12325
 * labia majora carcinoma
 * class of disease
 * vulva carcinoma skin cancer
 * Human disease
 * DOID:13389
 * labia minora cancer
 * class of disease
 * vulvar cancer skin cancer
 * Human disease
 * DOID:1243
 * labia minora carcinoma
 * class of disease
 * vulva carcinoma
 * Human disease
 * DOID:1293
 * labium majus cancer
 * class of disease
 * vulvar cancer
 * Human disease
 * DOID:11905
 * labyrinthine bilateral reactive loss
 * class of disease
 * labyrinthine dysfunction
 * Human disease
 * DOID:14413
 * labyrinthine unilateral reactive loss
 * class of disease
 * labyrinthine dysfunction
 * Human disease
 * DOID:1776
 * labyrinthitis
 * class of disease
 * otitis interna inner ear disease labyrinthosis disease
 * inflammation of the labyrinth, fluid-filled channels in the inner ear
 * DOID:1468
 * C09.218.568.558 C09.218.705.371
 * lacrimal apparatus disease
 * class of disease
 * eye disease eye adnexa disease rare palpebral, lacrimal system and conjunctival disease rare genetic palpebral, lacrimal system and conjunctival disease
 * human disease
 * DOID:1400
 * C11.496
 * lacrimal duct cancer
 * class of disease
 * lacrimal system cancer
 * Human disease
 * DOID:12756
 * lacrimal duct obstruction
 * class of disease
 * lacrimal apparatus disease stenosis and insufficiency of lacrimal passage
 * Human disease
 * DOID:13929
 * C11.496.456
 * Nasolacrimal duct obstruction
 * Tear system.svg
 * lacrimal gland adenocarcinoma
 * class of disease
 * lacrimal gland carcinoma adenocarcinoma
 * human disease
 * DOID:298
 * lacrimal gland cancer
 * class of disease
 * lacrimal system cancer lacrimal gland neoplasm
 * human disease
 * DOID:294
 * lacrimal gland carcinoma
 * class of disease
 * lacrimal gland cancer carcinoma
 * Human disease
 * DOID:293
 * lacrimal passage granuloma
 * class of disease
 * lacrimal apparatus disease
 * Human disease
 * DOID:10174
 * lacrimal system cancer
 * class of disease
 * ocular cancer lacrimal apparatus disease
 * human disease
 * DOID:292
 * lactic acidosis
 * class of disease
 * acidosis metabolic acidosis disease
 * acquired metabolic condition that has material basis in low pH in body tissues and blood accompanied by the buildup of lactate especially D-lactate
 * DOID:3650
 * C18.452.076.176.180
 * Lactic acidosis
 * lactose intolerance
 * class of disease
 * carbohydrate metabolic disorder malabsorption food intolerance disease
 * condition involving a decreased ability to digest lactose due to a lack of lactase in the small intestines, either genetically or from injury
 * DOID:10604
 * C06.405.469.637.506 C16.320.565.202.589 C18.452.603.506 C18.452.648.202.589
 * Lactose intolerance
 * Lactose(lac).png
 * lambda 5 deficiency
 * class of disease
 * B cell deficiency genetic disease monogenic disease
 * A B cell deficiency that has material basis in mutations in the IGLL1 gene. Lambda 5 mutations an cause a block in B cell development at the transition between the pro-B cell and the pre-B cell stage.
 * DOID:0060024
 * language disorder
 * class of disease
 * communication disorder
 * range of neurodevelopmental conditions
 * DOID:93
 * C10.597.606.150.500 C23.888.592.604.150.500
 * large bowel leiomyoma
 * class of disease
 * intestinal benign neoplasm leiomyoma benign neoplasm of large intestine
 * Human disease
 * DOID:5143
 * large cell carcinoma
 * class of disease
 * carcinoma
 * carcinoma that is composed of large, monotonous rounded or overtly polygonal-shaped cells with abundant cytoplasm
 * DOID:4552
 * C04.557.470.200.260
 * large cell carcinoma with rhabdoid phenotype
 * class of disease
 * large-cell lung carcinoma
 * Human disease
 * DOID:7480
 * large cell keratinizing variant squamous cell breast carcinoma
 * class of disease
 * breast squamous cell carcinoma keratinizing squamous cell carcinoma
 * Human disease
 * DOID:7461
 * large cell medulloblastoma
 * class of disease
 * medulloblastoma
 * medulloblastoma that is characterized by cells that are larger than would be normally expected
 * DOID:3857
 * large cell neuroendocrine carcinoma
 * class of disease
 * large cell carcinoma neuroendocrine carcinoma large-cell lung carcinoma
 * Human disease
 * DOID:0050872
 * Large cell neuroendocrine carcinoma
 * large cell neuroendocrine carcinoma of the lung
 * class of disease
 * large cell neuroendocrine carcinoma large-cell lung carcinoma pulmonary neuroendocrine tumor
 * human disease
 * DOID:6658
 * large intestine adenocarcinoma
 * class of disease
 * large intestine cancer adenocarcinoma
 * large intestine cancer that has material basis in epithelial cells of glandular origin
 * DOID:0050913
 * large intestine adenoma
 * class of disease
 * intestinal benign neoplasm gastrointestinal adenoma benign neoplasms by histologic type
 * intestinal benign neoplasm that has material basis in epithelial tissue with glandular origin and is located in the large intestine
 * DOID:0050914
 * large intestine cancer
 * class of disease
 * intestinal cancer colorectal neoplasm
 * intestinal cancer that effects the long, tube-like organ that is connected to the small intestine at one end and the anus at the other
 * DOID:5672
 * large intestine lipoma
 * class of disease
 * intestinal benign neoplasm lipoma benign neoplasm of large intestine
 * Human disease
 * DOID:6460
 * large-cell acanthoma
 * class of disease
 * acanthoma
 * Human disease
 * DOID:4321
 * large-cell lung carcinoma
 * class of disease
 * non-small-cell lung carcinoma large cell carcinoma disease
 * Disease
 * DOID:4556
 * Large-cell lung carcinoma
 * large-cell lymphoma
 * class of disease
 * lymphatic system cancer non-Hodgkin lymphoma
 * Human disease
 * DOID:8538
 * laryngeal adenoid cystic carcinoma
 * class of disease
 * laryngeal carcinoma
 * Human disease
 * DOID:4869
 * laryngeal cancer
 * class of disease
 * head and neck cancer carcinoma laryngeal neoplasm respiratory system cancer disease
 * respiratory system cancer that is located in the larynx
 * DOID:2596
 * Laryngeal cancer
 * Tumor Laryngis-01.jpg
 * laryngeal carcinoma
 * class of disease
 * laryngeal cancer carcinoma
 * larynx cancer that has material basis in epithelial cells
 * DOID:2600
 * laryngeal cartilage cancer
 * class of disease
 * laryngeal cancer
 * Human disease
 * DOID:13348
 * laryngeal disease
 * class of disease
 * upper respiratory tract disease
 * human disease
 * DOID:786
 * C08.360 C09.400
 * laryngeal mucoepidermoid carcinoma
 * class of disease
 * mucoepidermoid carcinoma laryngeal cancer
 * Human disease
 * DOID:4688
 * laryngeal neoplasm
 * class of disease
 * respiratory tract neoplasm laryngeal disease neoplasm respiratory system benign neoplasm
 * human disease
 * DOID:2598
 * C04.588.443.665.481 C08.360.369 C08.785.481 C09.400.369 C09.647.481
 * Neoplasms of larynx
 * laryngitis
 * class of disease symptom or sign
 * laryngeal disease inflammatory disease throat symptom disease
 * inflammation of the larynx
 * DOID:3437
 * C08.360.535 C08.730.368 C09.400.535 C01.748.368
 * Laryngitis
 * Laryngitis gastrica.jpg
 * laryngostenosis
 * class of disease
 * laryngeal disease
 * Human disease
 * DOID:11527
 * C08.360.591 C09.400.591 C16.131.740.658
 * laryngotracheitis
 * class of disease symptom or sign
 * upper respiratory tract disease throat symptom
 * human disease
 * DOID:0050148
 * larynx carcinoma in situ
 * class of disease
 * laryngeal disease in situ carcinoma
 * Human disease
 * DOID:9011
 * larynx leiomyoma
 * class of disease
 * laryngeal neoplasm leiomyoma
 * Human disease
 * DOID:10070
 * larynx leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * larynx sarcoma that is a smooth muscle connective tissue tymor located in the larynx
 * DOID:5288
 * larynx liposarcoma
 * class of disease
 * liposarcoma laryngeal cancer
 * liposarcoma that is located in the larynx
 * DOID:5696
 * larynx sarcoma
 * class of disease
 * laryngeal cancer sarcoma
 * larynx cancer that has material basis in abnormally proliferating cells derived from embryonic mesoderm
 * DOID:2877
 * larynx squamous papilloma
 * class of disease
 * laryngeal neoplasm squamous cell papilloma laryngeal papillomatosis
 * Human disease
 * DOID:10071
 * late congenital syphilis
 * class of disease
 * congenital syphilis
 * Human disease
 * DOID:10039
 * late yaws
 * class of disease
 * yaws
 * yaws that appears after five years of the initial infection and is characterized by disabling consequences of the nose, bones and palmar/plantar hyperkeratosis
 * DOID:10567
 * late-adult onset retinitis pigmentosa
 * class of disease
 * retinitis pigmentosa autosomal recessive disease
 * retinitis pigmentosa that is characterized by onset of symptoms in the fifth or sixth decade of life
 * DOID:0110421
 * lateral cystocele
 * class of disease
 * pelvic organ prolapse cystocele
 * Human disease
 * DOID:14130
 * lateral displacement of eye
 * class of disease
 * orbital disease exophthalmos
 * Human disease
 * DOID:12360
 * lateral medullary syndrome
 * class of disease
 * brain stem infarction
 * neurological disorder causing a range of symptoms due to ischemia in the lateral part of the medulla oblongata in the brainstem
 * DOID:3522
 * C10.228.140.300.150.477.100.500 C10.228.140.300.775.200.100.500 C14.907.253.092.477.100.500 C14.907.253.855.200.100.500 C23.550.513.355.250.100.500 C23.550.717.489.250.100.500
 * Lateral medullary syndrome
 * WallenbergInfarct001.jpg
 * lateral myocardial infarction
 * class of disease
 * myocardial infarction
 * Human disease
 * DOID:5853
 * lateral sinus thrombosis
 * class of disease
 * cerebral venous sinus thrombosis
 * Human disease
 * DOID:3574
 * C10.228.140.300.525.425.500.562 C14.907.253.566.350.500.562 C14.907.355.590.213.350.500.562
 * lateral ventricle meningioma
 * class of disease
 * intraventricular meningioma cerebral meningioma cerebral ventricle cancer
 * Human disease
 * DOID:6115
 * latex allergy
 * class of disease
 * allergy hazard disease
 * hypersensitivity reaction type I disease triggered by latex
 * DOID:0060532
 * C20.543.600
 * learning disability
 * class of disease
 * specific developmental disorder disability disease
 * range of neurodevelopmental conditions
 * DOID:8927
 * C10.597.606.150.550 C23.888.592.604.150.550 F03.625.562 F03.625.374.188
 * Learning disabilities
 * leech infestation
 * class of disease
 * ectoparasitism disease
 * human disease
 * DOID:11079
 * leg dermatosis
 * class of disease
 * skin disease
 * Human disease
 * DOID:3142
 * C17.800.446
 * legionellosis
 * class of disease
 * primary bacterial infectious disease
 * Human disease
 * DOID:10458
 * C01.150.252.400.500 C08.730.382 C01.748.382
 * legume allergy
 * class of disease
 * fruit allergy
 * human disease
 * DOID:0060904
 * leiomyoma
 * class of disease
 * benign neoplasms by histologic type smooth muscle tumour myoma disease
 * cell type benign neoplasm that is a benign tumor of smooth muscle cells
 * DOID:127
 * C04.557.450.590.450
 * Leiomyomas
 * Leiomyoma Uterus 40x.jpg
 * leiomyoma cutis
 * class of disease
 * dermis tumor skin benign neoplasm leiomyoma
 * benign tumor that arises from smooth muscle tissue in a hair follicle, forming a papule
 * DOID:5132
 * Cutaneous leiomyoma
 * leiomyomatosis
 * class of disease
 * leiomyoma
 * Human disease
 * DOID:5138
 * C04.557.450.590.450.465
 * leiomyosarcoma
 * class of disease
 * smooth muscle cancer disease
 * malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis
 * DOID:1967
 * C04.557.450.590.455 C04.557.450.795.455
 * Leiomyosarcoma
 * Cutaneous leiomyosarcoma - high mag.jpg
 * lens disease
 * class of disease
 * eye disease
 * Human disease
 * DOID:110
 * C11.510
 * lens subluxation
 * class of disease
 * lens disease
 * Human disease
 * DOID:11364
 * C11.510.598
 * lens-induced iridocyclitis
 * class of disease
 * iridocyclitis
 * Human disease
 * DOID:9388
 * leptomeninges sarcoma
 * class of disease
 * malignant leptomeningeal tumor meninges sarcoma sarcoma
 * Human disease
 * DOID:7689
 * lesion of sciatic nerve
 * class of disease
 * mononeuritis of lower limb
 * Human disease
 * DOID:12528
 * lethal congenital contracture syndrome 1
 * class of disease
 * lethal congenital contracture syndrome genetic disease
 * lethal congenital contracture syndrome that has material basis in homozygous or compound heterozygous mutation in the mRNA export mediator GLE1 on chromosome 9q34
 * DOID:0060559
 * leucine-sensitive hypoglycemia of infancy
 * class of disease
 * amino acid metabolic disorder autosomal dominant disease
 * human disease
 * DOID:0112262
 * leukemia
 * class of disease symptom or sign
 * hematologic cancer myeloproliferative disorders disease
 * group of cancers that usually begin in the bone marrow
 * DOID:1240
 * C04.557.337
 * Leukemias
 * Symptoms of leukemia.png
 * leukocoria
 * class of disease
 * pupil disorder eye degenerative disease
 * abnormal white reflection from the retina of the eye
 * DOID:11772
 * Leukocoria
 * Rb whiteeye.PNG
 * leukocyte adhesion deficiency 2
 * class of disease
 * leukocyte adhesion deficiency 3
 * leukocyte adhesion deficiency that is characterized by recurrent bacterial infections, severe growth delay and severe intellectual deficit
 * DOID:0080492
 * leukocyte disease
 * class of disease symptom or sign
 * hematopoietic system disease
 * disease involving the leukocyte
 * DOID:9500
 * C15.378.553
 * Leukocyte disorders
 * leukodystrophy
 * class of disease
 * cerebral degeneration disease
 * cerebral degeneration characterized by dysfunction of the white matter of the brain
 * DOID:10579
 * Leukodystrophies
 * leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
 * class of disease
 * nervous system heredodegenerative disease combined oxidative phosphorylation deficiency autosomal recessive disease
 * human disease
 * DOID:0111493
 * leukopenia
 * class of disease symptom or sign
 * leukocyte disease cytopenia hemic system symptom disease
 * decrease in the number of white blood cells
 * DOID:615
 * C15.378.553.546
 * leukoplakia of penis
 * class of disease
 * penile disease leukoplakia
 * Human disease
 * DOID:8738
 * leukoplakia of vagina
 * class of disease
 * vaginal disease leukoplakia
 * Human disease
 * DOID:8920
 * leukorrhea
 * class of disease
 * vaginal discharge disease
 * type of vaginal discharge
 * DOID:3766
 * C13.351.500.894.700.500
 * leukostasis
 * class of disease
 * leukocyte disease leukocytosis
 * human disease
 * DOID:12986
 * C15.378.553.560
 * lichen disease
 * class of disease
 * skin disease lichenoid eruption
 * Human disease
 * DOID:8574
 * lichen nitidus
 * class of disease
 * lichen disease
 * Human disease
 * DOID:8573
 * C17.800.859.475.545
 * Lichen nitidus
 * lichen planus
 * class of disease
 * lichen disease disease
 * chronic disease of skin, tongue or oral mucosa
 * DOID:9201
 * C17.800.859.475.560
 * Lichen planus
 * Lichen planus lip.jpg
 * lidocaine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger lidocaine
 * DOID:0040009
 * limb ischemia
 * class of disease
 * ischemia
 * Human disease
 * DOID:0050852
 * Limb ischemia
 * limb-girdle muscular dystrophy
 * class of disease
 * muscular dystrophy progressive muscular dystrophy disease
 * muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles
 * DOID:11724
 * C05.651.534.500.280 C10.668.491.175.500.149 C16.320.577.280
 * limbic encephalitis
 * class of disease
 * paraneoplastic neurologic syndrome encephalitis inflammatory and autoimmune disease with epilepsy autoimmune disease of the nervous system
 * Inflammation involving the limbic system in the brain
 * DOID:0080741
 * C04.588.614.550.450 C04.730.856.437 C10.228.140.430.525 C10.228.228.245.700 C10.574.781.550
 * limited scleroderma
 * class of disease
 * systemic scleroderma
 * the least progressive form of systemic scleroderma with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk
 * DOID:1577
 * C17.300.799.801 C17.800.784.801
 * linear skin defects with multiple congenital anomalies 1
 * class of disease
 * microphthalmia–dermal aplasia–sclerocornea syndrome X-linked dominant disease congenital disorder
 * human disease
 * DOID:0111808
 * lingual goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13196
 * C16.131.894.500.500 C19.874.283.802 C19.874.689.500.500
 * lingual-facial-buccal dyskinesia
 * class of disease
 * movement disorders
 * Human disease
 * DOID:9854
 * linitis plastica
 * class of disease
 * gastric diffuse adenocarcinoma stomach carcinoma disease
 * Human disease
 * DOID:4023
 * C04.557.470.200.025.095.410
 * Linitis plastica
 * lip disease
 * class of disease
 * mouth disease
 * human disease
 * DOID:9297
 * C07.465.409
 * Lip disorders
 * lipid metabolism disorder
 * class of disease
 * inherited metabolic disorder disease
 * high cholesterol & lipids
 * DOID:3146
 * C18.452.584
 * Dyslipidemia
 * Fig21Femme obese.jpg
 * lipid storage disease
 * class of disease
 * lysosomal storage disease disease
 * lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body&#39;s cells and tissues
 * DOID:9455
 * C16.320.565.398.641 C18.452.584.563.641 C18.452.648.398.641
 * Lipid storage disorders
 * lipid-cell variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:7967
 * lipid-rich breast carcinoma
 * class of disease
 * lipid-rich carcinoma bilateral breast cancer
 * lipid-rich carcinoma characterized by the presence of cytoplasmic neutral lipids in the vast majority of the malignant cells
 * DOID:7076
 * lipid-rich carcinoma
 * class of disease
 * breast carcinoma
 * breast carcinoma characterized by the presence of malignant epithelial cells with clear cytoplasm which contains neutral lipids
 * DOID:5658
 * lipoadenoma
 * class of disease
 * adenoma
 * adenoma that is composed of adipose tissue
 * DOID:5398
 * lipoatrophic diabetes
 * class of disease
 * type 2 diabetes
 * type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes
 * DOID:11712
 * C18.452.394.750.149.500 C19.246.300.500
 * lipoid nephrosis
 * class of disease
 * idiopathic nephrotic syndrome nephrotic syndrome disease
 * Human disease
 * DOID:10966
 * C12.777.419.630.477 C13.351.968.419.630.477
 * Minimal change disease
 * lipoma
 * class of disease
 * benign neoplasms by histologic type adipose tissue neoplasm disease
 * benign tumor made of fat tissue
 * DOID:3315
 * C04.557.450.550.400
 * Lipomas
 * Lipoma 02.jpg
 * lipoma of colon
 * class of disease
 * large intestine lipoma colonic disease
 * Human disease
 * DOID:10655
 * lipoma of spermatic cord
 * class of disease
 * paratesticular lipoma lipoma male reproductive organ benign neoplasm
 * Human disease
 * DOID:10206
 * lipoma of the rectum
 * class of disease
 * large intestine lipoma benign neoplasm of rectum
 * Human disease
 * DOID:6459
 * lipomatosis
 * class of disease
 * skin disease
 * Human disease
 * DOID:3153
 * C17.800.463 C18.452.584.718
 * Lipomatosis
 * liposarcoma
 * class of disease
 * lipomatous cancer sarcoma disease
 * lipomatous cancer that arises in fat cells in deep soft tissue retroperitoneum
 * DOID:3382
 * C04.557.450.550.420 C04.557.450.795.465
 * Liposarcoma
 * Myxoid liposarcoma (06).JPG
 * liposarcoma of bone
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3381
 * liposarcoma of the ovary
 * class of disease
 * ovary sarcoma liposarcoma sarcoma ovarian cancer
 * Human disease
 * DOID:5697
 * lissencephaly 3
 * class of disease
 * autosomal dominant disease lissencephaly
 * human disease
 * DOID:0112232
 * liver angiosarcoma
 * class of disease
 * angiosarcoma liver cancer hepatic vascular disease liver sarcoma organ type
 * angiosarcoma and sarcoma of liver and hemangioma of intra-abdominal structure and Ca liver - primary that is located in the liver
 * DOID:268
 * Liver angiosarcoma
 * Gross specimen of liver angiosarcoma.jpg
 * liver cancer
 * class of disease
 * liver tumor liver disease rare hepatic and biliary tract tumor liver neoplasm hepatobiliary system cancer endocrine gland cancer disease
 * human disease
 * DOID:3571
 * Liver cancer
 * Liver Cancer in Mouse Model (42507312762).jpg
 * liver carcinoma
 * class of disease
 * liver cancer carcinoma
 * liver cancer that has material basis in epithelial cells
 * DOID:686
 * liver carcinoma in situ
 * class of disease
 * in situ carcinoma liver disease
 * Human disease
 * DOID:9132
 * liver cirrhosis
 * class of disease
 * liver disease cirrosis disease
 * chronic disease of the liver, characterized by fibrosis
 * DOID:5082
 * C06.552.630 C23.550.355.412
 * Cirrhosis
 * Liver Cirrhosis.png
 * liver disease
 * class of disease
 * hepatobiliary disease endocrine system disease disease
 * disorder of the human liver
 * DOID:409
 * C06.552
 * Diseases and disorders of liver
 * liver fibroma
 * class of disease
 * liver neoplasm fibroma
 * Human disease
 * DOID:907
 * liver fibrosarcoma
 * class of disease
 * liver sarcoma fibrosarcoma
 * fibrosarcoma of soft tissue and sarcoma of liver that is located in the liver
 * DOID:8022
 * liver inflammatory pseudotumor
 * class of disease
 * Inflammatory pseudotumor inflammatory myofibroblastic tumour rare hepatic disease liver neoplasm rare hepatic and biliary tract tumor endocrine gland cancer liver disease
 * Human disease
 * DOID:918
 * liver leiomyoma
 * class of disease
 * liver neoplasm
 * Human disease
 * DOID:917
 * liver leiomyosarcoma
 * class of disease
 * liver sarcoma
 * leiomyosarcoma and sarcoma of liver that is located in the liver
 * DOID:5296
 * liver lipoma
 * class of disease
 * liver neoplasm gastrointestinal system benign neoplasm endocrine organ benign neoplasm
 * human disease
 * DOID:10190
 * liver lymphoma
 * class of disease
 * liver cancer endocrine gland cancer gastrointestinal lymphoma rare hepatic disease lymphoma
 * Human disease
 * DOID:901
 * liver neoplasm
 * class of disease
 * liver tumor hepatobiliary neoplasm liver disease endocrine organ benign neoplasm
 * human disease
 * DOID:916
 * C04.588.274.623 C06.301.623 C06.552.697
 * Benign neoplasms of liver
 * liver rhabdomyosarcoma
 * class of disease
 * liver sarcoma
 * rhabdomyosarcoma and sarcoma of liver that are located in the liver
 * DOID:4047
 * liver sarcoma
 * class of disease
 * liver cancer
 * sarcoma and malignant non-epithelial hepatic and intrahepatic bile duct neoplasm sthat is located in the liver
 * DOID:270
 * lobomycosis
 * class of disease
 * dermatomycosis disease
 * dermatomycosis that results in infection located in skin or located in subcutaneous tissue, has material basis in Lacazia loboi and has symptom crusty plaques, has symptom tumors and results in formation of nodular lesions
 * DOID:13026
 * C01.800.200.475 C01.150.703.302.475 C17.800.838.208.475
 * Lobomycosis
 * lobular neoplasia
 * class of disease
 * breast carcinoma in situ breast neoplasm
 * Human disease
 * DOID:3010
 * localized anterior staphyloma
 * class of disease
 * scleral staphyloma
 * Human disease
 * DOID:13787
 * localized chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5862
 * localized osteosarcoma
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3356
 * localized pulmonary fibrosis
 * class of disease
 * pulmonary fibrosis
 * Human disease
 * DOID:5642
 * localized scleroderma
 * class of disease
 * scleroderma
 * human disease
 * DOID:8472
 * C17.300.787 C17.800.767
 * Morphea
 * MercMorphea.JPG
 * locked-in syndrome
 * class of disease
 * neurological disorder disease
 * condition in which a patient is aware but cannot move or communicate verbally due to complete paralysis of nearly all voluntary muscles in the body except for vertical eye movements and blinking
 * DOID:12697
 * C10.597.622.760.500 C10.668.416 C23.888.592.636.786.500
 * CerebellumArteries.jpg
 * long QT syndrome 1
 * class of disease
 * long QT syndrome genetic disease autosomal dominant disease
 * A long QT syndrome that has material basis in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.
 * DOID:0110644
 * long QT syndrome 10
 * class of disease
 * long QT syndrome genetic disease autosomal dominant disease
 * A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.
 * DOID:0110651
 * long QT syndrome 4
 * class of disease
 * long QT syndrome autosomal dominant disease
 * human disease
 * DOID:0111701
 * long bone adamantinoma
 * class of disease
 * adamantinoma
 * adamantinoma that is located in the long bones and results in focal epithelial differentiation
 * DOID:2775
 * long bones of lower limb cancer
 * class of disease
 * bone cancer lower limb cancer
 * bone cancer that is manifested in the long bones of the lower limb
 * DOID:10149
 * loose anagen syndrome
 * class of disease
 * alopecia baldness
 * human disease
 * DOID:0111702
 * low compliance bladder
 * class of disease
 * bladder disease disease
 * human disease
 * DOID:12144
 * C12.777.829.866 C13.351.968.829.813 C23.888.942.343.780
 * low grade glioma
 * class of disease
 * glioma
 * A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma.
 * DOID:0080829
 * low implantation of placenta
 * class of disease
 * placenta praevia
 * Human disease
 * DOID:1677
 * low tension glaucoma
 * class of disease
 * open-angle glaucoma
 * Human disease
 * DOID:13544
 * C11.640.225
 * lower respiratory tract disease
 * class of disease
 * respiratory disease
 * respiratory system disease which involves the lower respiratory tract
 * DOID:0050161
 * lumbar plexus neoplasm
 * class of disease
 * nerve plexus neoplasm
 * Human disease
 * DOID:8389
 * lumbar spinal canal and spinal cord meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:7515
 * lumbosacral lipoma
 * class of disease
 * bone benign neoplasm lipoma
 * Human disease
 * DOID:7017
 * lumbosacral plexus lesion
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:13913
 * luminal breast carcinoma
 * class of disease
 * breast carcinoma breast carcinoma by gene expression profile
 * Human disease
 * DOID:0060548
 * luminal breast carcinoma B
 * class of disease
 * breast carcinoma luminal breast carcinoma
 * human disease
 * DOID:0080674
 * lung acinar adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * Human disease
 * DOID:6482
 * lung adenoid cystic carcinoma
 * class of disease
 * lung carcinoma adenoid cystic carcinoma
 * Human disease
 * DOID:4872
 * lung adenoma
 * class of disease
 * lung benign neoplasm benign epithelial neoplasm benign neoplasms by histologic type adenoma
 * Human disease
 * DOID:5386
 * lung benign neoplasm
 * class of disease
 * respiratory system benign neoplasm lung disease lung neoplasm thoracic cancer
 * human disease
 * DOID:3683
 * Benign neoplasms of bronchus and lung
 * lung carcinoma
 * class of disease
 * lung cancer carcinoma
 * lung cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the lungs and has symptom cough and has symptom chest discomfort or pain and has symptom weight loss and has symptom hemoptysis
 * DOID:3905
 * lung carcinoma in situ
 * class of disease
 * in situ carcinoma lung disease lung neoplasm
 * Human disease
 * DOID:8800
 * lung clear cell carcinoma
 * class of disease
 * clear cell carcinoma lung carcinoma
 * Human disease
 * DOID:7267
 * lung clear cell-sugar-tumor
 * class of disease
 * lung benign neoplasm perivascular epithelioid cell neoplasm benign perivascular tumor
 * Human disease
 * DOID:5763
 * lung combined large cell neuroendocrine carcinoma
 * class of disease
 * large cell neuroendocrine carcinoma of the lung combined carcinoma of lung
 * Human disease
 * DOID:7207
 * lung combined type small cell carcinoma
 * class of disease
 * lung small cell carcinoma combined carcinoma of lung
 * lung small cell carcinoma that is characterized as a multiphasic lung cancer comprised of a mixture of small cell and non-small cell lung carcinoma cells
 * DOID:5421
 * lung disease
 * class of disease
 * lower respiratory tract disease disease
 * respiratory disease
 * DOID:850
 * C08.381
 * lung hilum cancer
 * class of disease
 * lung cancer hilar lung neoplasm
 * Human disease
 * DOID:7696
 * lung leiomyoma
 * class of disease
 * lung benign neoplasm leiomyoma
 * Human disease
 * DOID:5136
 * lung leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * leiomyosarcoma and sarcoma of lung that is located in the lung
 * DOID:5265
 * lung lymphoma
 * class of disease
 * lung cancer lymphoma
 * Human disease
 * DOID:6760
 * lung meningioma
 * class of disease
 * lung cancer malignant neoplasm of meninges rare genetic respiratory disease genetic nervous system disorder ectopic meningioma
 * Human disease
 * DOID:5764
 * lung mixed small cell and squamous cell carcinoma
 * class of disease
 * pulmonary neuroendocrine tumor lung combined type small cell carcinoma
 * Human disease
 * DOID:7081
 * lung mucoepidermoid carcinoma
 * class of disease
 * lung carcinoma mucoepidermoid carcinoma
 * lung carcinoma that has material basis in a combination of squamous cells, mucus secreting cells and intermediate cells
 * DOID:0050932
 * Mucoepidermoid lung carcinoma
 * lung non-squamous non-small cell carcinoma
 * class of disease
 * non-small-cell lung carcinoma
 * lung non-small cell carcinoma that is characterized by the lack of evidence of squamous differentiation
 * DOID:0080521
 * lung oat cell carcinoma
 * class of disease
 * lung small cell carcinoma
 * Human disease
 * DOID:5411
 * lung occult adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * Human disease
 * DOID:7168
 * lung occult large cell carcinoma
 * class of disease
 * large-cell lung carcinoma lung occult non-small cell carcinoma
 * Human disease
 * DOID:7169
 * lung occult small cell carcinoma
 * class of disease
 * lung small cell carcinoma lung occult carcinoma
 * Human disease
 * DOID:5414
 * lung occult squamous cell carcinoma
 * class of disease
 * squamous cell carcinoma of the lung lung occult carcinoma
 * Human disease
 * DOID:6510
 * lung papillary adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung
 * Human disease
 * DOID:5588
 * lung sarcoma
 * class of disease
 * lung cancer sarcoma
 * lung cancer that is located in the lung and that arises from transformed cells of mesenchymal origin
 * DOID:2784
 * Primary pulmonary sarcoma, NOS - Case 299 (15760799904).jpg
 * lung small cell carcinoma
 * class of disease
 * lung carcinoma small cell carcinoma
 * lung carcinoma that has material basis in primitive-appearing cells that are smaller than normal cells
 * DOID:5409
 * C04.588.894.797.520.109.220.624 C08.381.540.140.750 C08.785.520.100.220.750
 * [[File:Combined small cell lung carcinoma with extensive mucosal involvement; possible SCLC in situ Case 271 (9255562385).jpg|center|64px]]
 * lung superior sulcus carcinoma
 * class of disease
 * Pancoast tumor
 * human disease
 * DOID:8208
 * lupus erythematosus
 * class of disease
 * autoimmune disease autoimmune disease of musculoskeletal system disease
 * human disease
 * DOID:8857
 * Butterflyrash.jpg
 * lupus nephritis
 * class of disease
 * glomerulonephritis disease
 * inflammation of the kidneys
 * DOID:0080162
 * C12.200.777.419.570.363.680 C12.050.351.968.419.570.363.680 C17.300.480.680 C20.111.590.560 C12.950.419.570.363.680
 * Lupus nephritis
 * luteoma
 * class of disease
 * ovarian benign neoplasm ovarian disease disease
 * ovarian benign neoplasm characterized by solid proliferations of luteinized cells, resulting in a tumor-like ovarian enlargement that regresses during the puerperium
 * DOID:7880
 * C04.557.475.750.751 C04.588.322.455.464 C13.351.500.056.630.705.464 C13.351.937.418.685.464 C19.344.410.464 C19.391.630.705.464
 * Luteoma of pregnancy
 * luxation of globe
 * class of disease
 * globe disease
 * Human disease
 * DOID:1241
 * lymph node adenoid cystic carcinoma
 * class of disease
 * lymph node metastasis carcinoma lymph node cancer lymph node carcinoma
 * Human disease
 * DOID:0060219
 * lymph node cancer
 * class of disease
 * lymphatic system cancer lymph node neoplasm lymph node disease
 * lymphatic system cancer that is located in the lymph node
 * DOID:10619
 * Lymph node cancers
 * lymph node carcinoma
 * class of disease
 * carcinoma lymph node cancer
 * human disease
 * DOID:0080618
 * lymph node disease
 * class of disease
 * lymphatic system disease
 * Human disease
 * DOID:9942
 * Diseases and disorders of lymph nodes
 * lymph node palisaded myofibroblastoma
 * class of disease
 * lymph node cancer benign neoplasm of lymph node
 * human disease
 * DOID:8304
 * lymphadenitis
 * class of disease symptom or sign
 * lymph node disease clinical sign lymphatic system symptom adenitis
 * lymph node and lymph vessels inflammation
 * DOID:1602
 * C15.604.315
 * lymphangioma
 * class of disease
 * lymphatic system malformation benign blood vessel neoplasm disease
 * malformations of the lymphatic system characterized by lesions that are thin-walled cysts
 * DOID:1475
 * C04.557.375.450
 * Lymphangiomas
 * Lymphangioma.jpg
 * lymphangiosarcoma
 * class of disease
 * lymphatic system cancer angiosarcoma associated with lymphedema skin carcinoma skin sarcoma disease
 * lymphatic system cancer that has material basis in endothelial cells located in lymphatic vessels
 * DOID:2689
 * C04.557.375.480 C04.557.450.795.480
 * lymphatic system cancer
 * class of disease
 * immune system cancer lymphatic system disease
 * immune system cancer that is located in the lymphatic system and is characterized by uncontrolled cellular proliferation of lymphoid tissue
 * DOID:0060073
 * lymphatic system disease
 * class of disease
 * immune disorder
 * immune system disease that is located in the lymphatic system
 * DOID:75
 * C15.604
 * lymphoblastic leukemia
 * class of disease
 * leukemia
 * leukemia that has material basis in lymphoblasts (immature white blood cells)
 * DOID:1037
 * lymphoblastic lymphoma
 * class of disease symptom or sign
 * non-Hodgkin lymphoma lymphoma lymphatic system symptom
 * lymphoma that has material basis in immature malignant lymphocytes (lymphoblasts) committed to the B-cell or T-cell lineage and located in primarily lymph nodes or located in extranodal sites
 * DOID:0080147
 * lymphocele
 * class of disease
 * lymphatic system disease
 * Human disease
 * DOID:4347
 * C04.182.430 C15.604.510
 * lymphocytic gastritis
 * class of disease
 * gastritis chronic gastritis
 * Human disease
 * DOID:4035
 * lymphoepithelioma-like acinar prostate adenocarcinoma
 * class of disease
 * prostate adenocarcinoma prostatic acinar adenocarcinoma
 * Human disease
 * DOID:7246
 * lymphoepithelioma-like carcinoma
 * class of disease
 * carcinoma large cell carcinoma
 * carcinoma that is a malignant epithelial neoplasm densely infiltrated by lymphoid cells
 * DOID:5660
 * Lymphoepithelioma-like carcinoma
 * lymphoepithelioma-like thymic carcinoma
 * class of disease
 * thymic carcinoma
 * Human disease
 * DOID:7599
 * lymphohistiocytoid mesothelioma
 * class of disease
 * malignant pleural mesothelioma sarcomatoid mesothelioma
 * Human disease
 * DOID:7381
 * lymphoid interstitial pneumonia
 * class of disease
 * idiopathic interstitial pneumonia lymphoproliferative disorders
 * Human disease
 * DOID:0050159
 * lymphoma
 * class of disease symptom or sign
 * hematologic cancer lymphatic system cancer lymphoma and pseudolymphoma lymphoid neoplasm disease
 * hematologic cancer that affects lymphocytes
 * DOID:0060058
 * C04.557.386 C15.604.515.569 C20.683.515.761
 * Lymphomas
 * Gastric MALT lymphoma 2.jpg
 * lymphoma-like variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:7972
 * lymphopenia
 * class of disease symptom or sign
 * leukopenia lymphatic system symptom disease
 * leukopenia that is the condition of having an abnormally low level of lymphocytes in the blood
 * DOID:614
 * C15.378.553.546.605 C20.673.627 C15.378.243.750.605
 * lymphoplasmacyte-rich meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:4591
 * lysosomal and lipase deficiency
 * class of disease
 * lipid storage disease
 * lipid storage disease characterized by lysosomal and lipase deficiency
 * DOID:0080217
 * macrocystic neurilemmoma
 * class of disease
 * neurilemmoma
 * Human disease
 * DOID:3203
 * macrocystic pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:7097
 * macrocytic anemia
 * class of disease symptom or sign
 * anemia
 * Human disease
 * DOID:2361
 * C15.378.071.252
 * macroglobulinemia
 * class of disease
 * plasma protein metabolism disease
 * Human disease
 * DOID:9080
 * macrotrabecular hepatoblastoma
 * class of disease
 * hepatoblastoma
 * Human disease
 * DOID:5798
 * macular degeneration
 * class of disease
 * retinal degeneration maculopathy blindness
 * retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye
 * DOID:4448
 * C11.768.585.439
 * Macular degeneration
 * Intermediate age related macular degeneration.jpg
 * macular hole
 * class of disease
 * retinal disease retinal perforation maculopathy
 * small break in the macula, located in the center of the eye&#39;s light-sensitive tissue called the retina
 * DOID:7633
 * Macular hole
 * macular keratitis
 * class of disease
 * keratitis
 * human disease
 * DOID:11871
 * macular retinal edema
 * class of disease
 * retinal edema maculopathy disease
 * Human disease
 * DOID:4449
 * C11.768.585.439.245
 * Macular edema
 * main bronchus cancer
 * class of disease
 * lung cancer
 * Human disease
 * DOID:3924
 * major depressive disorder
 * class of disease
 * depressive disorder mental depression disease
 * all-encompassing low mood accompanied by low self-esteem, and by loss of interest or pleasure in normally enjoyable activities
 * DOID:1470
 * F03.600.300.375
 * Major depressive disorder
 * Vincent Van Gogh - Sorrow.JPG
 * male breast cancer
 * class of disease
 * breast cancer male breast neoplasm
 * Human disease
 * DOID:1614
 * male genital organ stricture
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:12333
 * male genital organ vascular disease
 * class of disease
 * male reproductive system disease vascular disease
 * Human disease
 * DOID:12335
 * male infertility
 * class of disease symptom or sign
 * male reproductive system disease infertility sexual impotence disease
 * inability to father a child
 * DOID:12336
 * C12.294.365.700
 * Male infertility
 * male reproductive organ benign neoplasm
 * class of disease
 * reproductive organ benign neoplasm male reproductive system neoplasm male reproductive system disease
 * human disease
 * DOID:0060087
 * male reproductive organ cancer
 * class of disease
 * reproductive organ cancer male reproductive system neoplasm male reproductive system disease
 * cancer that is manifested in the male genital system
 * DOID:3856
 * male reproductive system disease
 * class of disease
 * reproductive system disease male urogenital disease
 * reproductive system disease that affects male reproductive organs
 * DOID:48
 * C12.294
 * Diseases and disorders of the male reproductive system
 * male urethral cancer
 * class of disease
 * urethral cancer
 * Human disease
 * DOID:736
 * maleic anhydride allergic asthma
 * class of disease
 * allergic asthma maleic anhydride exposure
 * allergic asthma that has allergic trigger maleic anhydride
 * DOID:0040049
 * malignant acrospiroma
 * class of disease
 * acrospiroma sweat gland cancer
 * Human disease
 * DOID:5570
 * Malignant acrospiroma
 * malignant adenofibroma
 * class of disease
 * carcinosarcoma
 * Human disease
 * DOID:4422
 * malignant adult ependymoma
 * class of disease
 * ependymal tumor anaplastic ependymoma
 * Human disease
 * DOID:5890
 * malignant anus melanoma
 * class of disease
 * anal cancer mucosal melanoma melanoma
 * Human disease
 * DOID:14145
 * malignant biphasic mesothelioma
 * class of disease
 * mesothelioma
 * Human disease
 * DOID:4486
 * malignant breast melanoma
 * class of disease
 * breast cancer
 * Human disease
 * DOID:4364
 * malignant cardiac germ cell tumor
 * class of disease
 * heart cancer
 * Human disease
 * DOID:14535
 * malignant cardiac peripheral nerve sheath neoplasm
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:14534
 * malignant childhood germ cell neoplasm
 * class of disease
 * pediatric germ cell tumor germ cell cancer childhood cancer
 * Human disease
 * DOID:8149
 * malignant ciliary body melanoma
 * class of disease
 * ciliary body cancer
 * Human disease
 * DOID:6524
 * malignant conjunctival melanoma
 * class of disease
 * conjunctival cancer ocular melanoma
 * Human disease
 * DOID:1751
 * malignant cystadenoma
 * class of disease
 * adenocarcinoma cystadenoma
 * human disease
 * DOID:60004
 * malignant cystic nephroma
 * class of disease
 * kidney cancer nephroblastoma childhood multilocular cystic kidney neoplasm kidney cortex disease
 * Human disease
 * DOID:7571
 * malignant dermis tumor
 * class of disease
 * skin cancer
 * Human disease
 * DOID:5274
 * malignant epithelial mesothelioma
 * class of disease
 * mesothelioma
 * Human disease
 * DOID:4489
 * malignant epithelioid hemangioendothelioma
 * class of disease
 * malignant hemangioma epithelioid hemangioendothelioma
 * A malignant hemangioma characterized by the presence of epithelioid endothelial cells. The neoplastic cells are arranged in cords and nests, which are embedded in a myxoid to hyalinized stroma.
 * DOID:0080190
 * malignant essential hypertension
 * class of disease
 * essential hypertension
 * Human disease
 * DOID:10823
 * malignant eyelid melanoma
 * class of disease
 * skin melanoma
 * Human disease
 * DOID:10040
 * malignant fibrous histiocytoma
 * class of disease
 * histiocytoma fibrous histiocytoma sarcoma
 * human disease
 * DOID:1907
 * malignant fibrous histiocytoma of bone
 * class of disease
 * connective tissue neoplasm osteosarcoma
 * Human disease
 * DOID:3352
 * malignant gastric germ cell tumor
 * class of disease
 * stomach cancer extragonadal germ cell cancer gastrointestinal system disease gastrointestinal system cancer
 * Human disease
 * DOID:6949 DOID:4716
 * malignant gastric granular cell tumor
 * class of disease
 * stomach cancer
 * Human disease
 * DOID:10536
 * malignant gastric teratoma
 * class of disease
 * malignant gastric germ cell tumor gastric teratoma extragonadal non-dysgerminomatous germ cell tumor
 * Human disease
 * DOID:6948
 * malignant giant cell tumor
 * class of disease
 * giant cell tumor connective tissue neoplasm
 * Human disease
 * DOID:2705
 * malignant giant cell tumor of soft parts
 * class of disease
 * malignant fibrous histiocytoma malignant giant cell tumor
 * Human disease
 * DOID:5638
 * malignant giant cell tumor of the tendon sheath
 * class of disease
 * synovium cancer
 * Human disease
 * DOID:2704
 * malignant glandular tumor of peripheral nerve sheath
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:8420
 * malignant granular cell esophageal tumor
 * class of disease
 * esophageal cancer granular cell tumor
 * Human disease
 * DOID:5040
 * malignant granular cell myoblastoma
 * class of disease
 * skin cancer malignant peripheral nerve neoplasm granular cell tumor
 * Human disease
 * DOID:5042
 * malignant granular cell skin tumor
 * class of disease
 * malignant dermis tumor malignant granular cell myoblastoma
 * Human disease
 * DOID:7639
 * malignant hemangioma
 * class of disease
 * sarcoma vascular cancer malignant mixed tumor
 * cell type cancer of vascular origin, characterized by proliferation of endothelial cells in and about the vascular lumen
 * DOID:0080189
 * malignant hypertension
 * class of disease symptom or sign
 * arterial hypertension hypertensive crisis disease
 * condition of markedly elevated blood pressure with diastolic pressure typically greater than 120 mm Hg
 * DOID:10824
 * C14.907.489.330
 * malignant hypertensive renal disease
 * class of disease
 * renal hypertension
 * Human disease
 * DOID:10177
 * malignant leptomeningeal tumor
 * class of disease
 * meningioma malignant neoplasm of meninges meningeal carcinomatosis
 * Human disease
 * DOID:6086
 * malignant mediastinal neurogenic neoplasm
 * class of disease
 * mediastinal cancer
 * mediastinal cancer that has material basis in neural cells
 * DOID:4691
 * malignant mediastinum hemangiopericytoma
 * class of disease
 * hemangiopericytoma hemangiopericytoma, malignant mediastinal cancer
 * hemangiopericytoma and sarcoma of the mediastinum that is located in the mediastinum
 * DOID:6209
 * malignant melanocytic neoplasm of the peripheral nerve sheath
 * class of disease
 * malignant peripheral nerve sheath tumor
 * Human disease
 * DOID:6345
 * malignant melanocytic peripheral nerve sheath tumor of mediastinum
 * class of disease
 * mediastinal cancer peripheral neuropathy malignant melanocytic neoplasm of the peripheral nerve sheath mediastinum sarcoma nervous system cancer
 * Human disease
 * DOID:7077
 * malignant mesenchymoma
 * class of disease
 * mesenchymoma
 * Human disease
 * DOID:5758
 * malignant mixed tumor
 * class of disease
 * Mixed tumor cell type cancer
 * cell type cancer that has material basis in cells from two tissues
 * DOID:154
 * C04.557.435.525
 * malignant neoplasm of acoustic nerve
 * class of disease
 * cranial nerve malignant neoplasm vestibulocochlear nerve neoplasm inner ear cancer vestibulocochlear nerve disease ear neoplasms
 * Human disease
 * DOID:2814
 * malignant neoplasm of short bones of lower limb
 * class of disease
 * long bones of lower limb cancer
 * Human disease
 * DOID:10151
 * malignant oculomotor nerve tumor
 * class of disease
 * cranial nerve III tumor cranial nerve malignant neoplasm
 * Human disease
 * DOID:2816
 * malignant otitis externa
 * class of disease
 * otitis externa complications of diabetes mellitus
 * Human disease
 * DOID:10516
 * malignant ovarian Brenner tumor
 * class of disease
 * ovarian cancer ovarian Brenner tumor malignant ovarian surface epithelial-stromal neoplasm
 * malignant ovarian surface epithelial-stromal neoplasm that has material basis in the surface epithelium of the ovary
 * DOID:4217
 * malignant ovarian cyst
 * class of disease
 * ovarian cancer ovarian cyst
 * Human disease
 * DOID:2145
 * malignant ovarian germ cell neoplasm
 * class of disease
 * ovarian germ cell neoplasm rare gynecological tumor germ cell cancer ovarian cancer
 * Human disease
 * DOID:2155
 * malignant ovarian surface epithelial-stromal neoplasm
 * class of disease
 * surface epithelial-stromal tumor ovarian cancer
 * Human disease
 * DOID:2151
 * malignant parietal pleura tumor
 * class of disease
 * pleural cancer
 * Human disease
 * DOID:14032
 * malignant pediatric adrenal gland pheochromocytoma
 * class of disease
 * adrenal gland pheochromocytoma
 * adrenal gland pheochromocytoma that is characterized by rare chromaffin cell tumors which secrete catecholamines, and has a higher prevalence of hereditary factors and metastatis in children than adults
 * DOID:0070325
 * malignant peripheral nerve sheath tumor
 * class of disease
 * nerve sheath neoplasms malignant peripheral nerve neoplasm
 * Human disease
 * DOID:5940
 * Malignant peripheral nerve sheath tumor
 * malignant peritoneal solitary fibrous tumor
 * class of disease
 * peritoneum cancer peritoneal solitary fibrous tumor
 * Human disease
 * DOID:4490
 * malignant pheochromocytoma
 * class of disease
 * adrenal medulla cancer
 * adrenal medulla cancer that arises within the adrenal medulla, releasing epinephrines and norepinephrines hormones
 * DOID:0080347
 * malignant pineal area germ cell neoplasm
 * class of disease
 * pinealoma
 * Human disease
 * DOID:1660
 * malignant pleural mesothelioma
 * class of disease
 * pleural cancer benign pleural mesothelioma mesothelioma squamous cell carcinoma respiratory system cancer pleural disease
 * pleural cancer that has material basis in mesothelium cells
 * DOID:7474
 * Pleural mesothelioma
 * malignant renovascular hypertension
 * class of disease
 * malignant secondary hypertension renovascular hypertension renal hypertension
 * Human disease
 * DOID:13730
 * malignant secondary hypertension
 * class of disease
 * secondary hypertension
 * Human disease
 * DOID:13731
 * malignant skin fibrous histiocytoma
 * class of disease
 * malignant dermis tumor malignant fibrous histiocytoma
 * Human disease
 * DOID:1906
 * malignant spindle cell melanoma
 * class of disease
 * melanoma hemangiopericytoma spindle cell cancer
 * melanoma that is most commonly located in sun-exposed skin and results in formation of spindle-like shaped cells that have a high recurrence rate even with treatment
 * DOID:3162
 * malignant spiradenoma
 * class of disease
 * eccrine sweat gland cancer apocrine sweat gland cancer spiradenoma
 * Human disease
 * DOID:7960
 * malignant struma ovarii
 * class of disease
 * struma ovarii immature teratoma of ovary
 * Human disease
 * DOID:5208
 * malignant syringoma
 * class of disease
 * eccrine sweat gland cancer
 * Human disease
 * DOID:5569
 * malignant triton tumor
 * class of disease
 * malignant peripheral nerve sheath tumor
 * human disease
 * DOID:6707
 * malignant tumor of undescended testis
 * class of disease
 * testicular cancer cryptorchidism
 * Human disease
 * DOID:12276
 * malignant type A thymoma
 * class of disease
 * spindle cell thymoma
 * Human disease
 * DOID:7927
 * malignant type AB thymoma
 * class of disease
 * mixed type thymoma
 * Human disease
 * DOID:6723
 * malignant visceral pleura tumor
 * class of disease
 * pleural cancer
 * Human disease
 * DOID:14033
 * malt worker's lung
 * class of disease
 * extrinsic allergic alveolitis
 * extrinsic allergic alveolitis which is caused by inhalation of fungal spores of Aspergillus clavatus and Aspergillus fumigatus from moldy barley
 * DOID:2314
 * mammary Paget's disease
 * class of disease
 * breast adenocarcinoma disease
 * type of cancer that may have the appearance of eczema, involving the nipple
 * DOID:3443
 * C04.557.470.200.240.187.500 C04.557.470.615.275.625
 * Paget's disease of the breast
 * mammary analogue secretory carcinoma
 * class of disease
 * salivary gland cancer carcinoma salivary gland carcinoma secretory carcinoma
 * salivary gland neoplasm
 * DOID:0080808
 * C04.557.470.200.588
 * mammary myofibroblastoma
 * class of disease
 * benign neoplasm muscle tissue neoplasm breast benign neoplasm
 * rare, benign tumor of the breast
 * DOID:1629
 * mantle cell lymphoma
 * class of disease
 * B-cell lymphoma aggressive B-cell non-Hodgkin lymphoma disease
 * B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles
 * DOID:0050746
 * C04.557.386.480.525 C15.604.515.569.480.525 C20.683.515.761.480.525
 * Mantle cell lymphoma
 * Mantle cell lymphoma - intermed mag.jpg
 * marasmus
 * class of disease
 * protein-energy malnutrition disease
 * form of severe malnutrition characterized by energy deficiency
 * DOID:12328
 * Marasmus
 * Starved child.jpg
 * marginal corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10441
 * marginal zone B-cell lymphoma
 * class of disease
 * B-cell lymphoma leukocyte disease
 * group of lymphomas
 * DOID:0050748
 * Marginal zone lymphoma - kidney -- high mag.jpg
 * mast cell leukemia
 * class of disease
 * leukemia rare bone disease mastocytoma
 * rare leukemia (blood cancer) involving mast cells
 * DOID:9254
 * C04.557.337.440 C04.557.337.539.275.440 C20.762.750.750.500
 * Mast cell leukemia
 * mast cell sarcoma
 * class of disease
 * sarcoma mastocytoma
 * human disease
 * DOID:355
 * C04.557.450.565.465.124 C20.762.750.375
 * Mast Cell Sarcoma.jpg
 * mastitis
 * class of disease symptom or sign
 * breast disease breastfeeding difficulties inflammatory disease reproductive system disease skin and integumentary tissue symptom disease
 * inflammation of the breast
 * DOID:10690
 * C13.703.844.603 C17.800.090.968
 * Mastitis
 * [[File:Atlas of clinical surgery; with special reference to diagnosis and treatment for practitioners and students (1908) (14768289625).jpg|center|64px]]
 * mastocytoma
 * class of disease
 * tumor of hematopoietic and lymphoid tissues myeloid neoplasm
 * solid tumor consisting of mast cells, generally benign
 * DOID:3664
 * C04.557.450.565.465.249 C20.762.750.469
 * Mastocytoma
 * mastoiditis
 * class of disease
 * bone inflammation disease middle ear disease disease
 * middle ear disease characterized by an inflammation of the mucosal lining of the mastoid antrum and the mastoid air cell system inside the mastoid process
 * DOID:0060322
 * C01.539.160.495.500 C05.116.165.495.249 C09.218.705.663.652
 * Mastoiditis
 * Mastoiditis1.jpg
 * mature B-cell neoplasm
 * class of disease
 * B-cell lymphoma
 * Human disease
 * DOID:706
 * mature T-cell and NK-cell lymphoma
 * class of disease
 * non-Hodgkin lymphoma mature T-cell neoplasm
 * non-Hodgkin lymphoma that has material basis in mature T lymphocytes and natural killer cells
 * DOID:0050743
 * mature cataract
 * class of disease
 * senile cataract
 * Human disease
 * DOID:13717
 * mature gastric teratoma
 * class of disease
 * gastric teratoma mature teratoma
 * Human disease
 * DOID:8118
 * mature teratoma
 * class of disease
 * teratoma
 * Human disease
 * DOID:5566
 * Mature teratoma Case 164 (5462532633).jpg
 * mature teratoma of the ovary
 * class of disease
 * mature teratoma ovarian biphasic or triphasic teratoma ovarian germ cell teratoma
 * Human disease
 * DOID:6231
 * Mature teratoma of ovary
 * maturity-onset diabetes of the young
 * class of disease
 * diabetes autosomal dominant disease disease
 * genetic disease that has material basis in mutations in the MODY genes disrupting insulin production
 * DOID:0050524
 * maturity-onset diabetes of the young type 14
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young that has material basis in heterozygous mutation in the APPL1 gene on chromosome 3p14
 * DOID:0111111
 * maturity-onset diabetes of the young type 2
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young that has material basis in heterozygous mutation in the GCK gene on chromosome 7p13
 * DOID:0111100
 * maturity-onset diabetes of the young type 3
 * class of disease
 * maturity-onset diabetes of the young
 * A maturity-onset diabetes of the young that has material basis in mutation in the HNF1A gene on chromosome 12q24.31.
 * DOID:0111102
 * maturity-onset diabetes of the young type 4
 * class of disease
 * maturity-onset diabetes of the young
 * A maturity-onset diabetes of the young that has material basis in mutation in the PDX1 gene on chromosome 13q12.2.
 * DOID:0111103
 * maturity-onset diabetes of the young type 5
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young characterized by abnormal renal development resuting in non-diabetic kidney disease and diabetes that has material basis in mutation in the HNF1B gene on chromosome 17q12
 * DOID:0111101
 * maturity-onset diabetes of the young type 6
 * class of disease
 * maturity-onset diabetes of the young
 * maturity-onset diabetes of the young that has material basis in heterozygous mutation in the NEUROD1 gene on chromosome 2q31
 * DOID:0111104
 * maxillary sinus cancer
 * class of disease
 * paranasal sinus cancer maxillary sinus neoplasm
 * Human disease
 * DOID:1357
 * maxillary sinus cholesteatoma
 * class of disease
 * paranasal sinus disease cholesteatoma mouth disease
 * cholesteatoma located in paranasal sinus
 * DOID:867
 * maxillary sinusitis
 * class of disease
 * nose disease sinusitis mouth disease
 * sinusitis which involves infection of maxillary sinuses that causes pain or pressure over the cheeks just below the eyes, tooth ache, and headache
 * DOID:2051
 * C08.460.692.752.578 C08.730.749.578 C09.603.692.752.578 C01.748.749.578
 * mechanical ectropion
 * class of disease
 * ectropion
 * Human disease
 * DOID:1569
 * mechanical entropion
 * class of disease
 * entropion
 * Human disease
 * DOID:13112
 * mechanical lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:13037
 * mechanical strabismus
 * class of disease
 * strabismus
 * Human disease
 * DOID:9306
 * meconium aspiration syndrome
 * class of disease
 * lung disease perinatal respiratory disorder disease
 * Human disease
 * DOID:11049
 * C08.381.520.687 C08.618.580 C13.703.277.785 C16.300.580 C16.614.580
 * Meconium aspiration syndrome
 * Amniotic fluid and meconium aspiration Case 179 (5613700230).jpg
 * medial epicondylitis
 * class of disease
 * bone inflammation disease arm injuries disease
 * bone inflammation disease that results in inflammation located in epicondyle
 * DOID:14087
 * Golfer's elbow
 * Golfers-Elbow SAG.jpg
 * median arcuate ligament syndrome
 * class of disease
 * vascular surgery rare abdominal surgical disease syndrome
 * Human disease
 * DOID:9892
 * C06.198.929C14.240.850.922 C14.907.137.527 C16.131.240.850.898
 * Median arcuate ligament syndrome
 * median nerve neuropathy
 * class of disease
 * mononeuritis of upper limb and mononeuritis multiplex brachial plexus neuritis
 * Human disease
 * DOID:571
 * C10.668.829.500.500
 * mediastinal cancer
 * class of disease
 * thoracic cancer mediastinal neoplasm
 * thoracic cancer that is located in the mediastinum
 * DOID:5559
 * Mediastinal cancers
 * mediastinal granular cell myoblastoma
 * class of disease
 * malignant mediastinal neurogenic neoplasm granular cell tumor mediastinal neurilemmoma
 * Human disease
 * DOID:5046
 * mediastinal gray zone lymphoma
 * class of disease
 * gray zone lymphoma mediastinal malignant lymphoma
 * Human disease
 * DOID:6867
 * mediastinal lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3926
 * MediastinalLipomatosisCT.png
 * mediastinal malignant lymphoma
 * class of disease
 * mediastinal cancer lymphoma
 * Human disease
 * DOID:6868
 * mediastinal melanocytic neurilemmoma
 * class of disease
 * melanotic neurilemmoma
 * Human disease
 * DOID:6484
 * mediastinal mesenchymal tumor
 * class of disease
 * mediastinal neoplasm mesenchymal cell neoplasm
 * Human disease
 * DOID:5560
 * mediastinal neurilemmoma
 * class of disease
 * peripheral nerve schwannoma mediastinal neoplasm
 * Human disease
 * DOID:6175
 * mediastinal osteogenic sarcoma
 * class of disease
 * extraosseous osteosarcoma mediastinum sarcoma
 * Human disease
 * DOID:6208
 * mediastinitis
 * class of disease
 * connective tissue disease mediastinal disease inflammatory disease disease
 * inflammatory process affecting the mediastinum
 * DOID:819
 * C08.846.187.790
 * mediastinum angiosarcoma
 * class of disease
 * angiosarcoma mediastinum sarcoma
 * angiosarcoma and sarcoma of the mediastinum that is located in the mediastinum
 * DOID:4525
 * mediastinum leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of mediastinum thoracic benign neoplasm mediastinal neurilemmoma
 * Human disease
 * DOID:5123
 * mediastinum leiomyosarcoma
 * class of disease
 * mediastinum sarcoma leiomyosarcoma
 * leiomyosarcoma and sarcoma of the mediastinum that derive from smooth muscle and are usually located in the esophagus or located in the main vessels
 * DOID:5292
 * mediastinum liposarcoma
 * class of disease
 * liposarcoma mediastinum sarcoma
 * liposarcoma and mediastinum sarcoma that is located in the mediastinum
 * DOID:5713
 * mediastinum neurofibroma
 * class of disease
 * malignant mediastinal neurogenic neoplasm neurofibroma
 * Human disease
 * DOID:12064
 * mediastinum rhabdomyosarcoma
 * class of disease
 * mediastinum sarcoma rhabdomyosarcoma
 * rhabdomyosarcoma and sarcoma of the mediastinum that is located in the mediastinum and affects children and adolescents
 * DOID:4049
 * mediastinum sarcoma
 * class of disease
 * mediastinal cancer sarcoma mediastinal soft tissue cancer
 * sarcoma and malignant mediastinal mesenchymnal tumor that is located in the mediastinum
 * DOID:4050
 * mediastinum seminoma
 * class of disease
 * mediastinal cancer extragonadal seminoma mediastinal malignant germ cell tumor germ cell cancer
 * Human disease
 * DOID:6249
 * mediastinum synovial sarcoma
 * class of disease
 * mediastinum sarcoma synovial sarcoma
 * sarcoma of the mediastinum and synovial sarcoma that is located in the mediastinum
 * DOID:5488
 * mediastinum teratoma
 * class of disease
 * mediastinal cancer mediastinal germ cell tumor teratoma
 * Human disease
 * DOID:5568
 * medullary colon carcinoma
 * class of disease
 * colon carcinoma
 * colon carcinoma that is characterized by a solid growth pattern
 * DOID:0080183
 * medulloadrenal hyperfunction
 * class of disease
 * adrenal gland disease
 * Human disease
 * DOID:12257
 * medulloblastoma SHH activated
 * class of disease
 * medulloblastoma
 * human disease
 * DOID:0080703
 * medulloblastoma SHH activated and TP53 mutant
 * class of disease
 * medulloblastoma SHH activated
 * human disease
 * DOID:0080704
 * medulloblastoma SHH activated and TP53 wild-type
 * class of disease
 * medulloblastoma SHH activated
 * human disease
 * DOID:0080705
 * medulloblastoma WNT activated
 * class of disease
 * medulloblastoma
 * human disease
 * DOID:0080702
 * medulloblastoma non-WNT/non-SHH
 * class of disease
 * medulloblastoma
 * human disease
 * DOID:0080706
 * medulloblastoma non-WNT/non-SHH group 3
 * class of disease
 * medulloblastoma non-WNT/non-SHH
 * human disease
 * DOID:0080707
 * medulloblastoma non-WNT/non-SHH group 4
 * class of disease
 * medulloblastoma non-WNT/non-SHH
 * human disease
 * DOID:0080708
 * medulloepithelioma
 * class of disease
 * central nervous system primitive neuroectodermal neoplasm
 * Human disease
 * DOID:4790
 * Medulloepithelioma
 * medullomyoblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3861
 * mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
 * class of disease
 * syndromic intellectual disability autosomal dominant disease
 * human disease
 * DOID:0111403
 * megacolon
 * class of disease
 * colonic disease disease
 * colonic disease that is characterized by an abnormal dilation of the colon
 * DOID:11372
 * C06.405.469.158.701
 * Megacolon
 * megaesophagus
 * class of disease
 * esophageal disease disease
 * abnormal dilation of the esophagus not due to obstruction
 * DOID:13186
 * megalencephalic leukoencephalopathy with subcortical cysts 1
 * class of disease
 * megalencephalic leukoencephalopathy with subcortical cysts genetic disease autosomal recessive disease
 * human disease
 * DOID:0080316
 * meibomian cyst
 * class of disease symptom or sign
 * internal hordeolum blepharitis disease
 * Cyst in the eyelid caused by chronic granulomatous inflammation of Meibomian gland
 * DOID:9903
 * C04.182.197 C11.338.300
 * Chalazion
 * Chalazion.JPG
 * melancholia
 * class of disease symptom or sign
 * major depressive disorder mental depression disease
 * DSM-IV subtype of clinical depression
 * DOID:2848
 * Accademia - La Meditazione by Domenico Fetti 1618.jpg
 * melanoacanthoma
 * class of disease
 * seborrheic keratosis
 * Human disease
 * DOID:11684
 * melanocytic psammomatous MPNST
 * class of disease
 * malignant melanocytic neoplasm of the peripheral nerve sheath
 * Human disease
 * DOID:6344
 * melanoma and neural system tumor syndrome
 * class of disease
 * hereditary neoplastic syndromes rare nervous system tumor rare genetic developmental defect during embryogenesis inherited nervous system cancer-predisposing syndrome nervous system cancer genetic nervous system disorder inherited tumor autosomal dominant disease syndrome
 * Melanoma and neural system tumor syndrome is an extremely rare tumor association characterized by dual predisposition to melanoma and neural system tumors (typically astrocytoma; see this term)
 * DOID:0111511
 * melanoma in congenital melanocytic nevus
 * class of disease
 * skin melanoma congenital melanocytic nevus
 * skin melanoma that arises from a congenital melanocytic nevus
 * DOID:0070327
 * melanoma with features of a Spitz nevus
 * class of disease
 * Spitzoid lesion melanoma skin melanoma
 * skin melanoma that is characterized by asymmetric shape, diameter greater than 1 cm, a lesion with a deep invasive component, and a high degree of cytologic atypia
 * DOID:0070326
 * Spitzoid melanoma
 * melanomatosis
 * class of disease
 * melanoma
 * Human disease
 * DOID:7206
 * melanotic medulloblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3868
 * melanotic neurilemmoma
 * class of disease
 * neurilemmoma
 * Human disease
 * DOID:3205
 * melanotic neuroectodermal tumor
 * class of disease
 * bone benign neoplasm neuroectodermal tumor
 * Human disease
 * DOID:166
 * C04.557.465.625.630 C04.557.580.625.630
 * Melanotic neuroectodermal tumor of infancy
 * Oral melanotic neuroectodermal tumor infancy LDRT 369 08.tif
 * melon allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Cucumis melo plant fruit food product.
 * DOID:0060509
 * melphalan allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger melphalan
 * DOID:0040066
 * membranous glomerulonephritis
 * class of disease
 * glomerulonephritis lupus nephritis disease
 * human disease
 * DOID:10976
 * C12.777.419.570.363.625 C13.351.968.419.570.363.625 C20.111.535
 * Membranous glomerulonephritis
 * meningeal melanocytoma
 * class of disease
 * central nervous system melanocytic neoplasm primary melanocytic tumor of central nervous system malignant neoplasm of meninges
 * Human disease
 * DOID:5900
 * meningeal melanoma
 * class of disease
 * malignant leptomeningeal tumor central nervous system melanocytic neoplasm
 * Human disease
 * DOID:6085
 * meningeal melanomatosis
 * class of disease
 * central nervous system melanocytic neoplasm melanomatosis malignant neoplasm of meninges
 * Human disease
 * DOID:8243
 * meninges hemangiopericytoma
 * class of disease
 * meningioma hemangiopericytoma malignant neoplasm of meninges
 * Human disease
 * DOID:4957
 * meninges sarcoma
 * class of disease
 * meningioma malignant neoplasm of meninges sarcoma
 * Human disease
 * DOID:7614
 * meningioma
 * class of disease
 * meningeal neoplasm central nervous system cancer disease
 * Tumor forms from meninges
 * DOID:3565
 * C04.557.580.520 C04.557.645.520 C04.588.614.250.580.500 C10.551.240.500.500
 * Meningioma
 * Contrast enhanced meningioma.jpg
 * meningitis
 * class of disease symptom or sign
 * encephalomyelitis central nervous system disease disease
 * inflammation of the membranes around the brain and spinal cord
 * DOID:9471
 * C10.228.614
 * Meningitis
 * Meninges-en.svg
 * meningocele
 * class of disease
 * spina bifida cephalocele
 * Human disease
 * DOID:1088
 * C10.500.680.598 C16.131.666.680.598 C23.300.707.968
 * meningococcal meningitis
 * class of disease
 * bacterial meningitis meningococcal disease
 * bacterial meningitis that has material basis in Neisseria meningitidis infection
 * DOID:0080176 DOID:9929
 * C01.150.252.223.500.750 C01.150.252.400.625.549.449 C10.228.228.180.500.750 C10.586.625.280.505 C01.207.180.500.750
 * meningoencephalitis
 * class of disease symptom or sign
 * central nervous system disease meningitis encephalitis neurological symptom disease
 * central nervous system disease that involves encephalitis which occurs along with meningitis
 * DOID:10554
 * C10.228.140.430.550 C10.228.228.245.550 C10.228.228.570 C01.207.245.550 C01.207.570 C10.586.250.550 C10.586.625.500
 * Méningo-encéphalite amibienne primitive.JPG
 * meningothelial meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:7212
 * meningovascular neurosyphilis
 * class of disease
 * tertiary neurosyphilis syphilitic meningitis
 * Human disease
 * DOID:0050491
 * mental depression
 * class of disease symptom or sign
 * mood disorder neurological and physiological symptom disease
 * state of low mood and aversion to activity, which can affect a person&#39;s thoughts, behavior, motivation, feelings, and sense of well-being
 * DOID:1596
 * F01.145.126.350
 * Depression (mood)
 * Depression-loss of loved one.jpg
 * mental disorder
 * class of disease
 * disease
 * distressing thought or behavior pattern
 * DOID:150
 * F03
 * Mental and behavioural diseases and disorders
 * Gautier - Salpetriere.JPG
 * mepivacaine allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger mepivacaine
 * DOID:0040010
 * meropenem allergy
 * class of disease
 * beta-lactam allergy allergic asthma
 * beta-lactam allergy that has allergic trigger meropenem
 * DOID:0040038
 * mesangial proliferative glomerulonephritis
 * class of disease
 * glomerulonephritis proliferative glomerulonephritis lupus nephritis
 * glomerulonephritis associated primarily with the mesangium
 * DOID:4783
 * mesenchymal cell neoplasm
 * class of disease
 * cell type cancer
 * Human disease
 * DOID:3350
 * mesenchymal chondrosarcoma
 * class of disease
 * chondrosarcoma mesenchymal cell neoplasm small cell sarcoma
 * Human disease
 * DOID:4545
 * C04.557.450.565.280.280 C04.557.450.795.300.280
 * mesenchymoma
 * class of disease
 * connective tissue neoplasm
 * Human disease
 * DOID:2668
 * C04.557.435.500
 * mesenteric adenitis
 * class of disease
 * lymphadenitis adenitis
 * lymphadenitis
 * DOID:10782
 * C06.844.520 C15.604.315.618
 * Mesenteric adenitis
 * mesenteric vascular occlusion
 * class of disease
 * peripheral vascular disease mesenteric ischemia
 * Human disease
 * DOID:13252
 * C06.405.469.675 C06.844.550 C14.907.137.534
 * mesocestoidiasis
 * class of disease
 * parasitic helminthiasis infectious disease
 * parasitic helminthiasis infectious disease that involves parasitic cestode infection caused by Mesocestoides lineatus resulting in nausea, diarrhea, abdominal discomfort and vomiting
 * DOID:0050253
 * metabolic acidosis
 * class of disease
 * acidosis acquired metabolic disease disease
 * lactic acidosis that has material basis in high levels of acid
 * DOID:0050758
 * Metabolic acidosis
 * metabolic disease
 * class of disease
 * disease nutritional and metabolic diseases
 * disease that involving errors in metabolic processes of building or degradation of molecules
 * DOID:0014667
 * C18.452
 * Metabolic diseases and disorders
 * Ragged red fibres - gtc - very high mag.jpg
 * metachronous kidney Wilms' tumor
 * class of disease
 * nephroblastoma
 * Human disease
 * DOID:5178
 * metachronous osteosarcoma of the bone
 * class of disease
 * osteosarcoma
 * Human disease
 * DOID:3379
 * metal allergy
 * class of disease
 * allergy
 * hypersensitivity reaction type I disease triggered by a metal
 * DOID:0060501
 * Metal allergies
 * metal metabolism disorder
 * class of disease
 * mineral metabolism disease inherited metabolic disorder
 * inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals
 * DOID:896
 * C16.320.565.618 C18.452.648.618
 * metanephric adenoma
 * class of disease
 * renal adenoma
 * Human disease
 * DOID:6404
 * Metanephric adenoma
 * metaphyseal dysplasia
 * class of disease
 * osteochondrodysplasia
 * osteochondrodysplasia that results in thinning and the tendency to fracture located in bone
 * DOID:0080019
 * metatypical basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4281
 * methemoglobinemia
 * class of disease
 * hemoglobinopathy disease
 * a form of toxic anemia characterized by the presence of methemoglobin in the blood
 * DOID:10783
 * C15.378.619
 * Methemoglobinemia
 * methotrexate-associated lymphoproliferation
 * class of disease
 * lymphoma
 * Human disease
 * DOID:5821
 * methyl isocyanate allergic asthma
 * class of disease
 * isocyanates allergic asthma
 * allergic asthma to isocyanates that has allergic trigger methyl isocyanate
 * DOID:0040044
 * methylmalonic acidemia cblB type
 * class of disease
 * methylmalonic acidemia genetic disease vitamin B12-responsive methylmalonic acidemia
 * Human disease
 * DOID:0060743
 * methylmalonic aciduria and homocystinuria type cblE
 * class of disease
 * methylmalonic acidemia methylmalonic acidemia with homocystinuria
 * Human disease
 * DOID:0050732
 * methylmalonic aciduria and homocystinuria type cblG
 * class of disease
 * methylmalonic acidemia methylmalonic acidemia with homocystinuria
 * Human disease
 * DOID:0050733
 * microcystic adenoma
 * class of disease
 * pancreatic cystadenoma benign neoplasms by histologic type
 * Human disease
 * DOID:5403
 * microcystic meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:4594
 * microcystic variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:7971
 * microglandular adenosis
 * class of disease
 * breast disease
 * Human disease
 * DOID:5998
 * microglandular adenosis of breast
 * class of disease
 * microglandular adenosis
 * Human disease
 * DOID:8335
 * microinvasive cervical squamous cell carcinoma
 * class of disease
 * cervical squamous cell carcinoma
 * Human disease
 * DOID:8409
 * microinvasive gastric cancer
 * class of disease
 * gastric adenocarcinoma
 * Human disease
 * DOID:10541
 * microlissencephaly
 * class of disease
 * lissencephaly
 * human disease
 * DOID:0112234
 * micronodular basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4289
 * microorchidism
 * class of disease
 * testicular disease hypogonadism, male
 * congenital human disease
 * DOID:11994
 * Microorchidism
 * Mikroorchie.jpg
 * micropapillary variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * Human disease
 * DOID:6976
 * micropapillomatosis labialis
 * class of disease
 * vulvar squamous papilloma Vestibular papillomatosis
 * Human disease
 * DOID:6569
 * microphthalmia with brain and digit anomalies
 * class of disease
 * syndromic microphthalmia autosomal dominant disease
 * human disease
 * DOID:0111805
 * microphthalmia–dermal aplasia–sclerocornea syndrome
 * class of disease
 * syndromic microphthalmia syndrome
 * human disease
 * DOID:0111875
 * microscopic breast papilloma
 * class of disease
 * breast duct papilloma
 * Human disease
 * DOID:8225
 * microscopic colitis
 * class of disease
 * colitis disease
 * colitis that can only be diagnosed by the examination of colon tissue under a microscope
 * DOID:0060182
 * C06.405.205.265.173 C06.405.469.158.188.173
 * Microscopic colitis
 * middle cerebral artery infarction
 * class of disease
 * cerebral arterial disease cerebral infarction cerebral artery occlusion
 * human disease
 * DOID:3525
 * C10.228.140.300.150.477.200.450 C10.228.140.300.510.200.387 C10.228.140.300.775.200.200.450 C14.907.253.092.477.200.450 C14.907.253.560.200.387 C14.907.253.855.200.200.450
 * middle ear adenoma
 * class of disease
 * sensory organ benign neoplasm middle ear disease neoplasm of middle ear benign neoplasms by histologic type benign neoplasm of ear
 * Human disease
 * DOID:5387
 * middle ear cancer
 * class of disease
 * neoplasm of middle ear auricular cancer middle ear disease
 * auditory system cancer that is located in the middle ear
 * DOID:5099
 * middle ear cholesterol granuloma
 * class of disease
 * otitis media cholesteatoma
 * Human disease
 * DOID:10852
 * middle lobe syndrome
 * class of disease
 * lung disease atelectasis
 * human disease
 * DOID:2810
 * C08.381.730.542
 * midface dysplasia
 * class of disease
 * osteochondrodysplasia disease
 * Human disease
 * DOID:0050767
 * midline cystocele
 * class of disease
 * pelvic organ prolapse cystocele
 * Human disease
 * DOID:14131
 * migraine
 * class of disease
 * encephalopathy disease
 * disorder resulting in recurrent moderate-severe headaches
 * DOID:6364
 * C10.228.140.546.399.750
 * Migraine
 * Migraine.jpg
 * migraine with aura
 * class of disease
 * migraine
 * migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon
 * DOID:10024
 * C10.228.140.546.399.750.250
 * migraine without aura
 * class of disease
 * migraine rare genetic headache disorder
 * migraine that is characterized by migraine headaches that are not accompanied by an aura
 * DOID:12783
 * C10.228.140.546.399.750.450
 * mild pre-eclampsia
 * class of disease
 * pre-eclampsia
 * pre-eclampsia characterized by the presence of hypertension without evidence of end-organ damage, in a woman who was normotensive before 20 weeks&#39; gestation
 * DOID:10590
 * miliaria
 * class of disease
 * sweat gland disease disease
 * Human disease
 * DOID:1382
 * C17.800.946.492
 * Miliaria (disease)
 * miliaria profunda
 * class of disease
 * miliaria
 * miliaria that is characterized by ductal occlusion of the papillary dermis causing the gland&#39;s secretions to leak between the superficial and deep layers of the skin resulting in a rapidly-spreading flesh-colored rash
 * DOID:0070320
 * miliaria pustulosa
 * class of disease
 * miliaria
 * miliaria that is characterized by pustules resulting from inflammation and bacterial infection
 * DOID:0070319
 * miliaria rubra
 * class of disease
 * miliaria
 * Human disease
 * DOID:11153
 * Miliaria rubra
 * milk allergy
 * class of disease
 * food allergy disease
 * type of food allergy caused by milk
 * DOID:4376
 * C20.543.480.370.500
 * Milk allergy
 * Koemelkallegie-Eczeem in knieholte.jpg
 * mineral metabolism disease
 * class of disease
 * acquired metabolic disease disorder of metabolite absorption and transport
 * acquired metabolic disease that is characterized by abnormal mineral metabolism
 * DOID:0050032
 * Disorders of mineral metabolism
 * minor vestibular glands adenoma
 * class of disease
 * vestibular gland benign neoplasm adenoma
 * Human disease
 * DOID:2075
 * mirror agnosia
 * class of disease
 * agnosia visual agnosia
 * agnosia that is a loss of the ability to acknowledge objects in the neglected field that are visible when a mirror reflects the object visible in the non-neglected field
 * DOID:0060144
 * mirror movement disorder
 * class of disease
 * synkinesis movement disorders
 * movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs
 * DOID:0111153
 * mitochondrial DNA depletion syndrome 12b
 * class of disease
 * autosomal recessive disease mitochondrial DNA depletion syndrome mitochondrial DNA depletion syndrome 12
 * human disease
 * DOID:0080335
 * mitochondrial DNA depletion syndrome 14
 * class of disease
 * mitochondrial DNA depletion syndrome
 * human disease
 * DOID:0080336
 * mitochondrial DNA depletion syndrome 15
 * class of disease
 * autosomal recessive disease mitochondrial DNA depletion syndrome
 * human disease
 * DOID:0080337
 * mitochondrial DNA depletion syndrome 17
 * class of disease
 * mitochondrial DNA depletion syndrome
 * human disease
 * DOID:0070448
 * mitochondrial DNA depletion syndrome 8b
 * class of disease
 * mitochondrial DNA depletion syndrome autosomal recessive disease
 * human disease
 * DOID:0070331
 * mitochondrial complex III deficiency
 * class of disease
 * mitochondrial disease
 * mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III
 * DOID:0111139
 * mitochondrial complex V (ATP synthase) deficiency
 * class of disease
 * mitochondrial disease mitochondrial complex deficiency
 * mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex
 * DOID:0111143
 * mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1
 * class of disease
 * mitochondrial complex V (ATP synthase) deficiency
 * human disease
 * DOID:0111748
 * mitochondrial complex V (ATP synthase) deficiency nuclear type 6
 * class of disease
 * mitochondrial complex V (ATP synthase) deficiency
 * human disease
 * DOID:0111749
 * mitochondrial nonsyndromic sensorineural deafness
 * class of disease
 * sensorineural hearing loss mitochondrial deafness
 * human disease
 * DOID:0111751
 * mitochondrial type mitochondrial complex I deficiency
 * class of disease
 * mitochondrial complex I deficiency
 * human disease
 * DOID:0112100
 * mitochondrial type mitochondrial complex I deficiency 1
 * class of disease
 * mitochondrial type mitochondrial complex I deficiency
 * human disease
 * DOID:0112101
 * mitral valve disease
 * class of disease
 * heart valve disease
 * Human disease
 * DOID:61
 * Mitral valve diseases
 * mitral valve insufficiency
 * class of disease
 * mitral valve disease valve insufficiency disease
 * disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood
 * DOID:11502
 * C14.280.484.461
 * Mitral valve insufficiency
 * mitral valve stenosis
 * class of disease
 * mitral valve disease heart valve stenosis disease
 * mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart
 * DOID:1754
 * C14.280.484.517
 * Mitral valve stenosis
 * mixed astrocytoma-ependymoma
 * class of disease
 * mixed glioma
 * Human disease
 * DOID:7907
 * mixed astrocytoma-ependymoma-oligodendroglioma
 * class of disease
 * mixed glioma
 * Human disease
 * DOID:7817
 * mixed cell adenoma
 * class of disease
 * adenoma
 * Human disease
 * DOID:5385
 * mixed cell type adenoma of parathyroid
 * class of disease
 * parathyroid adenoma mixed cell adenoma
 * Human disease
 * DOID:7610
 * mixed cell type kidney Wilms' tumor
 * class of disease
 * nephroblastoma
 * Human disease
 * DOID:5179
 * mixed cerebral palsy
 * class of disease
 * cerebral palsy
 * subtype of cerebral palsy characterized by both the tight muscle tone of spastic cerebral palsy and the writhing, involuntary muscle movements of athetoid cerebral palsy
 * DOID:0050673
 * mixed ductal-endocrine carcinoma
 * class of disease
 * pancreatic ductal adenocarcinoma
 * Human disease
 * DOID:7716
 * mixed endometrial stromal and smooth muscle tumor
 * class of disease
 * uterine corpus cancer
 * Human disease
 * DOID:8302
 * mixed epithelial stromal tumour
 * class of disease
 * malignant mixed tumor
 * Human disease
 * DOID:5088
 * mixed epithelial tumor of ovary
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:6211
 * mixed epithelial/mesenchymal metaplastic breast carcinoma
 * class of disease
 * breast metaplastic carcinoma
 * Human disease
 * DOID:7541
 * mixed extragonadal germ cell cancer
 * class of disease
 * mixed germ cell cancer
 * mixed germ cell cancer that is located in areas of the body other than the ovary or testicle
 * DOID:0050907
 * mixed fibrolamellar hepatocellular carcinoma
 * class of disease
 * fibrolamellar hepatocellular carcinoma
 * fibrolamellar carcinoma that is characteirzed by the presence of both pure fibrolamellar hepatocellular carcinoma and conventional hepatocellular carcinoma components
 * DOID:0080182
 * mixed germ cell cancer
 * class of disease
 * germ cell cancer
 * germ cell cancer that occurs in many forms
 * DOID:3306
 * Mixed germ cell neoplasia
 * mixed germ cell-sex cord neoplasm
 * class of disease
 * malignant mixed tumor sex cord-gonadal stromal tumor
 * Human disease
 * DOID:2996
 * mixed glioma
 * class of disease
 * glioma
 * Human disease
 * DOID:5076
 * mixed gonadal dysgenesis X0/XY
 * class of disease
 * Turner syndrome gonadal dysgenesis disease
 * intersex variation
 * DOID:14449 DOID:0080656
 * C12.706.316.309.391 C12.706.316.795.249 C13.351.875.253.309.391 C13.351.875.253.795.249 C16.131.260.830.835.249 C16.131.939.316.309.391 C16.131.939.316.795.249 C16.320.180.830.835.249 C19.391.119.309.391 C19.391.119.795.249
 * mixed hepatoblastoma
 * class of disease
 * hepatoblastoma
 * Human disease
 * DOID:5789
 * mixed lacrimal gland cancer
 * class of disease
 * lacrimal gland cancer
 * Human disease
 * DOID:296
 * mixed liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5703
 * mixed malaria
 * class of disease
 * malaria
 * malaria that involves infection with more than one species of Plasmodium at the same time
 * DOID:14325
 * mixed oligodendroglioma-astrocytoma
 * class of disease
 * mixed glioma
 * Human disease
 * DOID:7912
 * mixed phenotype acute leukemia with MLL rearranged
 * class of disease
 * acute biphenotypic leukaemia
 * human disease
 * DOID:0081037
 * mixed phenotype acute leukemia, B/myeloid
 * class of disease
 * acute biphenotypic leukaemia
 * human disease
 * DOID:0081038
 * mixed receptive-expressive language disorder
 * class of disease
 * communication disorder
 * neurodevelopmental condition
 * DOID:12685
 * mixed sleep apnea
 * class of disease
 * sleep apnea
 * human disease
 * DOID:0080302
 * mixed testicular germ cell tumor
 * class of disease
 * testicular malignant germ cell cancer mixed germ cell cancer
 * mixed germ cell cancer that is located in the testis
 * DOID:4743
 * mixed type rhabdomyosarcoma
 * class of disease
 * rhabdomyosarcoma
 * Human disease
 * DOID:4065
 * mixed type thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:3280
 * mixed-type liposarcoma
 * class of disease
 * liposarcoma
 * Human disease
 * DOID:5709
 * mollusc allergy
 * class of disease
 * shellfish allergy
 * shellfish allergy triggered by Mollusca
 * DOID:0060523
 * molybdenum cofactor deficiency type A
 * class of disease
 * molybdenum cofactor deficiency genetic disease
 * human disease
 * DOID:0111164
 * monoclonal gammopathy of uncertain significance
 * class of disease
 * monoclonal gammopathy blood protein disease
 * human disease
 * DOID:7442
 * C15.378.147.542.640 C15.378.147.780.570 C20.683.460.640 C20.683.780.640
 * monoclonal paraproteinemia
 * class of disease
 * plasma protein metabolism disease paraproteinemia monoclonal gammopathy
 * Human disease
 * DOID:2346
 * monocular esotropia
 * class of disease
 * esotropia
 * Human disease
 * DOID:10293
 * monocular exotropia
 * class of disease
 * exotropia
 * Human disease
 * DOID:11853
 * monocyte, dendritic cell, and NK cell deficiency
 * class of disease
 * combined immunodeficiency
 * human disease
 * DOID:0111966
 * monocytic leukemia
 * class of disease
 * myeloid leukemia
 * type of myeloid leukemia characterized by a dominance of monocytes in the marrow
 * DOID:8527
 * monodermal teratoma
 * class of disease
 * ovarian germ cell teratoma
 * Human disease
 * DOID:5207
 * monofixation syndrome
 * class of disease
 * strabismus
 * Human disease
 * DOID:9843
 * Monofixation syndrome
 * monogenic disease
 * class of disease
 * genetic disease
 * Human disease
 * DOID:0050177
 * mononeuritis
 * class of disease
 * mononeuropathy
 * Human disease
 * DOID:1802
 * mononeuritis multiplex
 * class of disease
 * mononeuritis of upper limb and mononeuritis multiplex
 * Human disease
 * DOID:1835
 * mononeuritis of lower limb
 * class of disease
 * mononeuritis
 * Human disease
 * DOID:9473
 * mononeuritis of upper limb
 * class of disease
 * mononeuritis of upper limb and mononeuritis multiplex
 * Human disease
 * DOID:1844
 * mononeuritis of upper limb and mononeuritis multiplex
 * class of disease
 * mononeuritis
 * Human disease
 * DOID:572
 * mononeuropathy
 * class of disease
 * peripheral neuropathy disease
 * neuropathy that is characterized by damage to a single nerve, which results in loss of movement, sensation, or other function of that nerve
 * DOID:1188
 * C10.668.829.500
 * monophasic synovial sarcoma
 * class of disease
 * synovial sarcoma
 * Human disease
 * DOID:5495
 * mood disorder
 * class of disease
 * mental disorder
 * any of various disorders characterised primarily by disturbance in an individual&#39;s mood
 * DOID:3324
 * F03.600
 * Mood disorders
 * morbid obesity
 * class of disease
 * obesity
 * human disease
 * DOID:11981
 * C18.654.726.500.700 C23.888.144.699.500.500 E01.370.600.115.100.160.120.699.500.500 G07.100.100.160.120.699.500.500
 * Obesity
 * Morbid Obesity.jpg
 * morpheaform basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4292
 * morphine dependence
 * class of disease
 * opiate dependence
 * opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance
 * DOID:2560
 * C25.775.675.600
 * mosaic variegated aneuploidy syndrome
 * class of disease
 * syndrome aneuploidy
 * human disease
 * DOID:0080688
 * mosaic variegated aneuploidy syndrome 3
 * class of disease
 * autosomal recessive disease mosaic variegated aneuploidy syndrome
 * human disease
 * DOID:0080689
 * motility-related diarrhea
 * class of disease
 * diarrhea
 * Human disease
 * DOID:0050131
 * motor neuritis
 * class of disease
 * motor neuron disease
 * Human disease
 * DOID:683
 * motor neuron disease
 * class of disease
 * neurological disorder neurodegeneration disease
 * group of neurological disorders affecting motor neurons
 * DOID:231
 * C10.574.562 C10.668.467
 * Motor neuron diseases
 * mouth cancer
 * class of disease
 * gastrointestinal system cancer mouth disease oral cavity neoplasm head and neck cancer disease
 * gastrointestinal system cancer that is located in the oral cavity
 * DOID:8618
 * Oral cancer
 * ZungenCa2a.jpg
 * mouth disease
 * class of disease
 * gastrointestinal system disease stomatognathic disease disease of anatomical entity disease
 * gastrointestinal system disease that is located in the mouth
 * DOID:403
 * C07.465
 * Diseases and disorders of oral cavity, salivary glands and jaws
 * movement disorders
 * class of disease
 * encephalopathy motor dysfunction disease
 * clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements
 * DOID:480
 * C10.228.662
 * Movement disorders
 * mpox
 * class of disease symptom or sign notifiable disease
 * viral infectious disease Poxviridae infectious disease zoonosis disease
 * viral disease
 * DOID:3292
 * C01.925.256.743.615 C22.735.750 C22.795.600
 * Monkeypox
 * Monkeypox.jpg
 * mu chain disease
 * class of disease
 * heavy chain disease
 * heavy chain disease that results from an overproduction of mu antibody (IgM)
 * DOID:0060128
 * mucin-rich endometrial endometrioid adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:7293
 * mucinosis
 * class of disease
 * connective tissue disease metabolic disease
 * human disease
 * DOID:3141
 * C17.300.550
 * Mucinoses
 * mucinous adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, which produce mucin
 * DOID:3030
 * C04.557.470.200.025.075 C04.557.470.590.075
 * Pseudomyxoma peritonei
 * Invasive mucinous adenocarcinoma Case 250 (8207252350).jpg
 * mucinous adenofibroma
 * class of disease
 * adenofibroma
 * Human disease
 * DOID:2700
 * mucinous cystadenocarcinoma
 * class of disease
 * cystadenocarcinoma mucinous tumor
 * cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with a capsulated structure and mucus-producing cells
 * DOID:3603
 * C04.557.470.200.025.480.225 C04.557.470.590.480.225
 * [[File:Mucinous cystic tumor, atypical, uncertain malignant potential Case 252 (8211727496).jpg|center|64px]]
 * mucinous cystadenocarcinoma of the lung
 * class of disease
 * adenocarcinoma of the lung mucinous cystadenocarcinoma
 * lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue
 * DOID:0080304
 * mucinous cystadenofibroma
 * class of disease
 * cystadenofibroma
 * benign neoplasm characterized by the presence of cystic structures lined by mucinous columnar epithelial cells in a fibrotic stroma
 * DOID:6468
 * mucinous intrahepatic cholangiocarcinoma
 * class of disease
 * intrahepatic cholangiocarcinoma bile duct mucinous adenocarcinoma
 * Human disease
 * DOID:7024
 * mucinous lung adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung mucinous adenocarcinoma
 * lung adenocarcinoma with tumor cells floating in pools of mucin that distend alveolar spaces
 * DOID:0080303
 * mucinous ovarian cystadenoma
 * class of disease
 * ovarian cystadenoma mucinous cystadenoma
 * Human disease
 * DOID:3267
 * Mucinous cystoadenoma of the ovary
 * Mucinous Cystadenoma of Ovary (218889489).jpg
 * mucinous pancreas adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma mucinous adenocarcinoma
 * human disease
 * DOID:0080782
 * mucinous stomach adenocarcinoma
 * class of disease
 * gastric diffuse adenocarcinoma mucinous adenocarcinoma
 * Human disease
 * DOID:3716
 * mucinous tubular and spindle cell carcinoma
 * class of disease
 * renal cell carcinoma tubulopathy spindle cell carcinoma
 * human disease
 * DOID:4472
 * Mucinous tubular and spindle cell carcinoma
 * Renal Mucinous spindle 1.JPG
 * mucocele of appendix
 * class of disease
 * intestinal disease mucocele
 * Human disease
 * DOID:13248
 * mucoepidermoid esophageal carcinoma
 * class of disease
 * esophageal carcinoma mucoepidermoid carcinoma
 * Human disease
 * DOID:4686
 * mucoepidermoid thyroid carcinoma
 * class of disease
 * thyroid carcinoma mucoepidermoid carcinoma thyroid gland adenocarcinoma
 * Human disease
 * DOID:4687
 * mucolipidosis type III gamma
 * class of disease
 * pseudo-Hurler polydystrophy mucolipidosis autosomal recessive disease
 * human disease
 * DOID:0080678
 * mucopolysaccharidosis IV
 * class of disease
 * human disease
 * DOID:0050808
 * mucopolysaccharidosis Ih
 * class of disease
 * autosomal recessive disease mucopolysaccharidosis I
 * human disease
 * DOID:0111390
 * mucopolysaccharidosis Ih/s
 * class of disease
 * autosomal recessive disease mucopolysaccharidosis I
 * human disease
 * DOID:0111389
 * mucopolysaccharidosis type IIIA
 * class of disease
 * Sanfilippo syndrome autosomal recessive disease
 * human disease
 * DOID:0111395
 * mucopolysaccharidosis type IIIB
 * class of disease
 * Sanfilippo syndrome autosomal recessive disease
 * human disease
 * DOID:0111394
 * mucopolysaccharidosis type IIIC
 * class of disease
 * autosomal recessive disease Sanfilippo syndrome
 * human disease
 * DOID:0111393
 * mucopolysaccharidosis type IIID
 * class of disease
 * autosomal recessive disease Sanfilippo syndrome
 * human disease
 * DOID:0111402
 * mucopolysaccharidosis type IVA
 * class of disease
 * Morquio syndrome autosomal recessive disease
 * human disease
 * DOID:0111391
 * mucopolysaccharidosis type IVB
 * class of disease
 * autosomal recessive disease Morquio syndrome
 * human disease
 * DOID:0111392
 * mucormycosis
 * class of disease symptom or sign
 * zygomycosis opportunistic mycosis disease
 * fungal infection by the order Mucorales
 * DOID:8485 DOID:0050595
 * C01.150.703.980.600
 * [[File:Periorbital fungal infection known as mucormycosis, or phycomycosis PHIL 2831 lores.jpg|center|64px]]
 * mucosal melanoma
 * class of disease
 * melanoma extracutaneous melanoma
 * melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract
 * DOID:0050929
 * mucositis
 * class of disease
 * skin disease gastrointestinal system disease
 * gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract
 * DOID:0080178
 * C06.405.205.798 C07.465.584
 * Mucositis
 * multicentric papillary thyroid carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:7086
 * multicentric reticulohistiocytosis
 * class of disease
 * Reticulohistiocytosis syndrome
 * syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis
 * DOID:11824
 * multifocal dystonia
 * class of disease
 * dystonia
 * dystonia that involves two or more unrelated body parts
 * DOID:0050837
 * multifocal osteogenic sarcoma
 * class of disease
 * osteosarcoma bone sarcoma
 * Human disease
 * DOID:3360
 * multilocular cystic clear cell renal cell carcinoma
 * class of disease
 * renal cell carcinoma renal clear cell carcinoma
 * human disease
 * DOID:4463
 * multiminicore disease
 * class of disease
 * human disease
 * DOID:0080991
 * multinodular goiter
 * class of disease
 * goiter nodular goiter
 * goiter characterized by a multinodular enlargement of the thyroid gland
 * DOID:0050489
 * multiple benign circumferential skin creases on limbs
 * class of disease
 * skin disease
 * human disease
 * DOID:0112241
 * multiple chemical sensitivity
 * class of disease
 * syndrome
 * chronic medical condition of disputed but probably multifactorial etiology (genetic and non-genetic)
 * DOID:4661
 * C20.543.312.500 C21.223.500
 * Multiple chemical sensitivity
 * multiple congenital anomalies-hypotonia-seizures syndrome
 * class of disease
 * lipid metabolism disorder
 * lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency
 * DOID:0080503
 * multiple cranial nerve palsy
 * class of disease
 * glossopharyngeal nerve disease cranial nerve disease
 * Human disease
 * DOID:13866
 * multiple endocrine neoplasia
 * class of disease
 * endocrine gland neoplasm multiple polyglandular tumor
 * human disease
 * DOID:3125
 * C04.588.322.400 C04.651.600 C04.700.630 C16.320.700.630 C19.344.400
 * Multiple endocrine neoplasia
 * multiple epiphyseal dysplasia 2
 * class of disease
 * multiple epiphyseal dysplasia genetic disease autosomal dominant disease multiple epiphyseal dysplasia due to collagen 9 anomaly
 * multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A2 gene on chromosome 1p34
 * DOID:0070298
 * multiple epiphyseal dysplasia 3
 * class of disease
 * multiple epiphyseal dysplasia genetic disease multiple epiphyseal dysplasia due to collagen 9 anomaly autosomal dominant disease
 * multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A3 gene on chromosome 20q13
 * DOID:0070304
 * multiple epiphyseal dysplasia 7
 * class of disease
 * multiple epiphyseal dysplasia genetic disease autosomal recessive disease
 * multiple epiphyseal dysplasia that has material basis in homozygous mutation in the CANT1 gene on chromosome 17q25
 * DOID:0070302
 * multiple epiphyseal dysplasia due to collagen 9 anomaly
 * class of disease
 * multiple epiphyseal dysplasia genetic disease monogenic disease
 * multiple epiphyseal dysplasia that has material basis in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3)
 * DOID:0070305
 * multiple epiphyseal dysplasia with myopia and deafness
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0111348
 * multiple mitochondrial dysfunctions syndrome 6
 * class of disease
 * fatal multiple mitochondrial dysfunctions syndrome autosomal recessive disease
 * human disease
 * DOID:0070332
 * multiple mucosal neuroma
 * class of disease
 * neuroma
 * Human disease
 * DOID:5155
 * multiple myeloma
 * class of disease
 * leukocyte disease myeloid neoplasm immunoproliferative disorder disease
 * cancer of plasma cells
 * DOID:9538
 * C04.557.595.500 C14.907.454.460 C15.378.147.780.650 C15.378.463.515.460 C20.683.515.845 C20.683.780.650
 * Multiple myeloma
 * Plasmozytom multiple Osteolysen Unterarm.png
 * multiple spinal canal and spinal cord meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:7646
 * multisystem proteinopathy
 * class of disease
 * motor neuron disease
 * human disease
 * DOID:070355
 * mumps
 * class of disease symptom or sign
 * parotitis mumps virus infectious disease herpangina salivary gland disease disease
 * Human disease caused by paramyxovirus
 * DOID:10264
 * C01.925.782.580.600.680.500 C07.465.815.470.800.630
 * Mumps
 * Mumps.jpg
 * muscle neoplasm
 * class of disease
 * soft tissue neoplasm muscular disease
 * tumors or cancer located in muscle tissue or specific muscles
 * DOID:461
 * C04.588.839.500 C05.651.494
 * muscle tissue disease
 * class of disease
 * muscular disease
 * disease involving the muscle tissue
 * DOID:66
 * muscular atrophy
 * class of disease
 * muscular disease atrophic muscular disease clinical sign
 * human disease
 * DOID:767
 * C10.597.613.612 C23.300.070.500 C23.888.592.608.612
 * Muscle wasting
 * musculoskeletal disorder
 * class of disease
 * disease of anatomical entity
 * disease of anatomical entity that occurs in the muscular and/or skeletal system
 * DOID:17
 * C05
 * Diseases and disorders of the musculoskeletal system
 * Ankle Joint Arthritis.jpg
 * musculoskeletal system benign neoplasm
 * class of disease
 * organ system benign neoplasm musculoskeletal neoplasm
 * organ system benign neoplasm that is located in the muscular and skeletal organs
 * DOID:0060099
 * musculoskeletal system cancer
 * class of disease
 * organ system cancer musculoskeletal disorder musculoskeletal neoplasm
 * organ system cancer located in the muscular and skeletal organs and characterized by uncontrolled cellular proliferation of the musculoskeletal organs
 * DOID:0060100
 * mushroom workers' lung
 * class of disease
 * extrinsic allergic alveolitis
 * Human disease
 * DOID:2708
 * mycoplasma infection
 * class of disease
 * bacterial infectious disease primary Mycoplasmataceae infectious disease disease
 * bacterial infection with a species of the genus Mycoplasma
 * DOID:0050407 DOID:5461
 * C01.150.252.400.610.610
 * mycosis fungoides
 * class of disease
 * cutaneous T cell lymphoma rare disease mycosis fungoides and variants disease
 * Human disease
 * DOID:8691
 * C04.557.386.480.750.800.550 C15.604.515.569.480.750.800.550 C20.683.515.761.480.750.800.550
 * Mycosis fungoides
 * Mycosis fungoides knee.JPG
 * mycotic corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10440
 * myelitis
 * class of disease
 * spinal cord disease
 * spinal cord disease that is characterized by inflammation of the white matter or gray matter of the spinal cord
 * DOID:322
 * C10.228.228.618 C10.228.854.525
 * Myelitis
 * Living anatomy and pathology; (1910) (14571685858).jpg
 * myelodysplastic syndrome
 * class of disease
 * myeloproliferative disorders neoplastic syndrome disease
 * diverse collection of blood-related medical conditions with ineffective production of the myeloid class of blood cells
 * DOID:0050908
 * C15.378.190.625
 * Myelodysplastic syndrome
 * myelodysplastic/myeloproliferative neoplasm
 * class of disease
 * myeloid neoplasm
 * myeloid neoplasm that results in the overproduction of white blood cells
 * DOID:4972
 * myelofibrosis
 * class of disease
 * myeloid neoplasm acquired aplastic anemia rare genetic immune disease disease
 * myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue
 * DOID:4971
 * C15.378.190.636.765
 * Myelofibrosis, Reticulin Stain (6032644716).jpg
 * myeloid and lymphoid neoplasms associated with FGFR1 abnormalities
 * class of disease
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint
 * DOID:0080167
 * myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
 * class of disease
 * myeloid neoplasm associated with PDGFRA rearrangement myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRA gene, most often resulting in the formation of FIP1L1-PDGFRA fusion transcripts
 * DOID:0080165
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * class of disease
 * myeloid neoplasm myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1
 * human disease
 * DOID:0080164
 * myeloid leukemia
 * class of disease
 * leukemia disease
 * leukemia that is located in myeloid tissue
 * DOID:8692
 * C04.557.337.539
 * Myeloid leukemias
 * myeloid leukemia associated with Down Syndrome
 * class of disease
 * acute megakaryoblastic leukemia
 * human disease
 * DOID:0080798
 * myeloid neoplasm
 * class of disease
 * myeloproliferative disorders
 * a bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages.
 * DOID:0070004
 * myeloid neoplasms associated with PDGFRB rearrangement
 * class of disease
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRB gene, most often resulting in the formation of ETV6-PDGFRB fusion transcripts
 * DOID:0080166
 * myeloid sarcoma
 * class of disease
 * hematologic cancer
 * solid tumor composed of immature white blood cells[2] called myeloblasts.
 * DOID:8683
 * C04.557.337.539.775 C04.557.450.795.853
 * Myeloid sarcoma
 * myelophthisic anemia
 * class of disease
 * aplastic anemia
 * aplastic anemia that is characterized by displacement of hemopoietic bone-marrow tissue either by fibrosis, tumors or granulomas
 * DOID:2354
 * C15.378.071.307 C15.378.190.636.085
 * myeloproliferative disorder, chronic, with eosinophilia
 * class of disease
 * myeloproliferative disorders eosinophilia myeloproliferative neoplasm
 * human disease
 * DOID:0111344
 * myeloproliferative disorders
 * class of disease
 * bone marrow disease tumor of hematopoietic and lymphoid tissues connective tissue neoplasm hematologic cancer disease
 * hematopoietic disorders that derive from the blood-forming stem cells of the bone marrow
 * DOID:4960
 * C15.378.190.636
 * Myeloid neoplasms
 * myeloproliferative neoplasm
 * class of disease
 * myeloid neoplasm myeloproliferative disorders
 * myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood
 * DOID:2226
 * myoblastoma
 * class of disease
 * muscle neoplasm
 * human disease
 * DOID:5039
 * myocardial stunning
 * class of disease
 * myocardial infarction
 * state when some section of the myocardium (corresponding to area of a major coronary occlusion) shows a form of contractile abnormality
 * DOID:9767
 * C14.280.671 C23.888.582
 * myocarditis
 * class of disease symptom or sign
 * extrinsic cardiomyopathy myocardial disorder pancarditis cardiovascular system symptom disease
 * extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle
 * DOID:820
 * C14.280.238.625
 * Myocarditis
 * Viral myocarditis (1).JPG
 * myocardium cancer
 * class of disease
 * neoplasm of myocardium heart cancer
 * human disease
 * DOID:9299
 * myoclonic cerebellar dyssynergia
 * class of disease
 * neurodegeneration nervous system heredodegenerative disease Ramsay Hunt syndrome
 * degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment
 * DOID:12707
 * C10.228.140.252.700.250 C10.228.854.787.500 C10.574.500.825.250 C16.320.400.780.500
 * myoclonic dystonia 11
 * class of disease
 * myoclonic dystonia genetic disease autosomal dominant disease
 * myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has material basis in heterozygous mutation in the SGCE gene on chromosome 7q21
 * DOID:0090034
 * myoclonic dystonia 15
 * class of disease
 * myoclonic dystonia genetic disease autosomal dominant disease
 * myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11
 * DOID:0090035
 * myoepithelial carcinoma
 * class of disease
 * carcinoma
 * carcinoma that derives from myoepithelial cells
 * DOID:4838
 * myoepithelioma of the head and neck
 * class of disease
 * sweat gland neoplasm
 * neoplasm composed of outgrowths of myoepithelial cells from a sweat gland
 * DOID:2661
 * C04.557.435.585
 * Myoepithelioma of the head and neck
 * myofascial pain syndrome
 * class of disease
 * muscular disease medically unexplained physical symptom myalgia disease
 * human disease
 * DOID:431
 * C05.651.550
 * myofibrillar myopathy
 * class of disease
 * muscular disease
 * myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles
 * DOID:0080307
 * myofibrillar myopathy 10
 * class of disease
 * autosomal recessive disease myofibrillar myopathy
 * human disease
 * DOID:0112108
 * myofibrillar myopathy 3
 * class of disease
 * myofibrillar myopathy autosomal dominant disease
 * Human disease
 * DOID:0080094
 * myofibroma
 * class of disease
 * connective tissue neoplasm benign perivascular tumor connective tissue benign neoplasm
 * Human disease
 * DOID:4386
 * C04.557.450.565.540 C17.300.680.540
 * Lipoleiomyoma uterus.jpg
 * myoma
 * class of disease
 * muscle neoplasm uterine benign neoplasm disease
 * human disease
 * DOID:2691
 * C04.557.450.590.540
 * Uterine fibroids
 * Uterine fibroids.jpg
 * myopathy of extraocular muscle
 * class of disease
 * peripheral neuropathy rare eye disease muscular disease
 * myopathy that involves the extra-ocular muscle
 * DOID:929
 * myopathy, lactic acidosis, and sideroblastic anemia 1
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * human disease
 * DOID:0111185
 * myopathy, lactic acidosis, and sideroblastic anemia 2
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has material basis in homozyous or compound heterozygous mutation in YARS2 on 12p11.21.
 * DOID:0111186
 * myopathy, lactic acidosis, and sideroblastic anemia 3
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * human disease
 * DOID:0111184
 * myopathy, myofibrillar, 11
 * class of disease
 * myofibrillar myopathy
 * human disease
 * DOID:0081338
 * myopia
 * class of disease symptom or sign
 * refractive error visual impairment disease
 * visual defect which causes to see the near objects clearly and far objects unclearly
 * DOID:11830
 * C11.744.636
 * Myopia
 * Myopia.gif
 * myosarcoma
 * class of disease
 * musculoskeletal system cancer muscle tissue neoplasm muscular disease
 * musculoskeletal system cancer that is located in muscle
 * DOID:4045
 * C04.557.450.590.550 C04.557.450.795.550
 * myositis
 * class of disease
 * muscular disease inflammation disease
 * myopathy characterized by muscle inflammation
 * DOID:633
 * C05.651.594 C10.668.491.562
 * myositis fibrosa
 * class of disease
 * myositis
 * Human disease
 * DOID:9788
 * myositis ossificans
 * class of disease
 * myositis heterotopic ossification
 * myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles
 * DOID:668
 * C05.651.594.638
 * myotonic cataract
 * class of disease
 * cataract
 * Human disease
 * DOID:82
 * myotonic disease
 * class of disease
 * muscular dystrophy
 * muscular dystrophy characterized by progressive muscle wasting and weakness
 * DOID:450
 * C05.651.662 C10.668.491.606
 * myringitis bullosa hemorrhagica
 * class of disease
 * tympanic membrane disease disease
 * tympanic membrane disease that is characterized by blisters on the eardrum resulting from infection
 * DOID:13791
 * myxedema
 * class of disease
 * hypothyroidism mucinosis disease
 * Human disease
 * DOID:11634
 * C17.300.550.590 C19.874.482.638
 * Myxedema
 * myxofibrosarcoma
 * class of disease
 * fibrous histiocytoma skeletal muscle cancer rare nervous system tumor peripheral neuropathy fibrosarcoma fibromyxoid tumor sarcoma
 * A malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.
 * DOID:0080534
 * myxoid chondrosarcoma
 * class of disease
 * chondrosarcoma myxoid tumor
 * human disease
 * DOID:5861
 * myxoid leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5268
 * myxoid liposarcoma of the ovary
 * class of disease
 * liposarcoma of the ovary myxoid liposarcoma
 * Human disease
 * DOID:8023
 * myxomatous pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8081
 * myxopapillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5075
 * myxosarcoma
 * class of disease
 * sarcoma connective tissue neoplasm
 * human disease
 * DOID:4136
 * C04.557.450.565.560 C04.557.450.795.560
 * nail disease
 * class of disease
 * integumentary system disease
 * integumentary system disease that is located in nail
 * DOID:4123
 * C17.800.529
 * Diseases and disorders of the nails
 * nanophthalmos
 * class of disease
 * microphthalmia
 * human disease
 * DOID:0080634
 * narcissistic personality disorder
 * class of disease
 * personality disorder narcissism disease
 * personality disorder that involves an excessive preoccupation with issues of personal adequacy, power, prestige and vanity
 * DOID:2745
 * F03.675.500
 * Narcissistic personality disorder
 * Seesaw narcissism megalomania model.png
 * narcolepsy
 * class of disease
 * disease sleep disorder excessive daytime sleepiness
 * Human sleep disorder that involves an excessive urge to sleep and other neurological features
 * DOID:8986
 * C10.886.425.800.200.750 F03.870.400.800.200.750
 * Narcolepsy
 * nasal cavity cancer
 * class of disease
 * sensory system cancer nasal cancer nasal cavity neoplasm nasal cavity disease respiratory system cancer
 * respiratory system cancer that is located in the nasal cavity
 * DOID:10811
 * nasal cavity disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:2163
 * nasal cavity lymphoma
 * class of disease
 * nasal cavity cancer lymphoma
 * human disease
 * DOID:10813
 * nasal cavity olfactory neuroblastoma
 * class of disease
 * nasal cavity cancer esthesioneuroblastoma
 * Human disease
 * DOID:10812
 * nasopharyngeal disease
 * class of disease
 * upper respiratory tract disease pharyngeal diseases
 * respiratory disease
 * DOID:9561
 * C07.550.350 C09.775.350
 * nasopharyngitis
 * class of disease
 * nasopharyngeal disease
 * respiratory disease
 * DOID:10460
 * C07.550.350.700 C07.550.781.500 C08.730.561.500 C09.775.350.700 C09.775.649.500
 * natural killer cell leukemia
 * class of disease
 * lymphoblastic leukemia leukocyte disease rare bone disease immune disorder disease
 * Human disease
 * DOID:1035
 * near-fatal asthma
 * class of disease
 * acute asthma
 * human disease
 * DOID:0080823
 * necrobiosis lipoidica
 * class of disease
 * skin disease diabetic dermadrome necrobiotic disorders
 * human disease
 * DOID:3486
 * C17.300.200.495.545 C17.800.550.545 C17.800.849.495 C18.452.880.495
 * Necrobiosis lipoidica
 * Necrobiosislipoidica.jpg
 * necrosis of ear ossicle
 * class of disease
 * middle ear disease ear disease
 * Human disease
 * DOID:11783
 * necrosis of pituitary
 * class of disease
 * pituitary gland disease
 * endocrine disease
 * DOID:3646
 * necrotizing enterocolitis
 * class of disease
 * gastrointestinal system disease disease
 * human disease
 * DOID:8677
 * C06.405.205.596.700 C06.405.469.363.700
 * Neonatal necrotizing enterocolitis
 * necrotizing fasciitis
 * class of disease symptom or sign
 * fasciitis necrotizing soft tissue infection disease
 * infection that results in the death of the body&#39;s soft tissue
 * DOID:9602
 * C01.252.825.340 C05.321.550
 * Necrotizing fasciitis
 * Necrotizing fasciitis left leg.JPEG
 * necrotizing gastritis
 * class of disease
 * gastritis necrosis chronic gastritis
 * Human disease
 * DOID:4037
 * necrotizing sialometaplasia
 * class of disease
 * salivary gland disease disease
 * Human disease
 * DOID:12901
 * C07.465.815.802
 * Necrotizing sialometaplasia
 * nemaline myopathy 2
 * class of disease
 * nemaline myopathy genetic disease autosomal recessive disease
 * nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23
 * DOID:0110928
 * nemaline myopathy 3
 * class of disease
 * nemaline myopathy genetic disease autosomal recessive disease
 * nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42
 * DOID:0110927
 * neomycin sulfate allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis drug allergy
 * allergic contact dermatitis that has allergic trigger neomycin sulfate
 * DOID:0040067
 * neonatal anemia
 * class of disease
 * anemia
 * Human disease
 * DOID:11244
 * C15.378.071.363 C16.614.053
 * neonatal diabetes mellitus
 * class of disease
 * diabetes neonatal metabolic disturbances rare genetic diabetes mellitus
 * It is a congenital form of diabetes
 * DOID:11717
 * neonatal infective mastitis
 * class of disease
 * mastitis perinatal infectious disease
 * Human disease
 * DOID:13520
 * neonatal jaundice
 * class of disease
 * pigmentation disorder jaundice neonatal hyperbilirubinemia disease
 * pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant
 * DOID:2383
 * C16.614.451.500 C23.550.429.249.500
 * Neonatal jaundice
 * Jaundice phototherapy.jpg
 * neonatal leukemia
 * class of disease
 * childhood leukemia perinatal disease
 * Human disease
 * DOID:7756
 * neonatal myasthenia gravis
 * class of disease
 * myasthenia gravis
 * Human disease
 * DOID:14043
 * C10.114.656.650 C10.668.758.725.650 C20.111.258.500.650
 * neonatal period electroclinical syndrome
 * class of disease
 * electroclinical syndrome perinatal disease
 * electroclinical syndrome with onset in the neonatal period less than 44 weeks of gestational age
 * DOID:0050702
 * neonatal thyrotoxicosis
 * class of disease
 * thyrotoxicosis
 * endocrine disease
 * DOID:12573
 * neonatal urinary tract infectious disease
 * class of disease
 * urinary system disease urinary tract infection in children perinatal infectious disease
 * Human disease
 * DOID:1375
 * neonatal-onset type II citrullinemia
 * class of disease
 * citrullinemia autosomal recessive disease citrullinemia type II
 * human disease
 * DOID:0070341
 * neovascular glaucoma
 * class of disease
 * glaucoma glaucoma associated with vascular disorder rare acquired eye disease
 * Human disease
 * DOID:1687
 * C11.525.381.348
 * nephritis
 * class of disease symptom or sign
 * urological symptom disease
 * inflammation of the kidneys
 * DOID:10952
 * C12.777.419.570 C13.351.968.419.570
 * Nephritis
 * Diffuse proliferative lupus nephritis.jpg
 * nephrocalcinosis
 * class of disease
 * kidney disease calcinosis
 * Human disease
 * DOID:12679
 * C12.050.351.968.419.590 C12.200.777.419.590 C18.452.174.130.560 C12.950.419.590
 * Nephrocalcinosis
 * nephrogenic adenofibroma
 * class of disease
 * kidney benign neoplasm
 * Human disease
 * DOID:2698
 * nephrogenic adenoma of the urethra
 * class of disease
 * urethral benign neoplasm nephrogenic adenoma adenoma
 * Human disease
 * DOID:8109
 * nephrogenic adenoma of urinary bladder
 * class of disease
 * bladder benign neoplasm nephrogenic adenoma adenoma
 * Human disease
 * DOID:7333
 * nephrogenic diabetes insipidus type 2
 * class of disease
 * autosomal dominant disease nephrogenic diabetes insipidus autosomal recessive disease
 * human disease
 * DOID:0081061
 * nephrolithiasis
 * class of disease
 * kidney disease kidney stone disease
 * Human disease
 * DOID:585
 * C12.200.777.419.600 C12.200.777.967.249 C12.050.351.968.419.600 C12.050.351.968.967.249 C12.950.419.600 C12.950.967.249
 * nephroma
 * class of disease
 * kidney benign neoplasm kidney cortex disease
 * human disease
 * DOID:0080615
 * nephronophthisis
 * class of disease
 * autosomal recessive disease medullary cystic kidney disease kidney disease
 * congenital disorder of urinary system
 * DOID:12712
 * Nephronophthisis
 * nephronophthisis 1
 * class of disease
 * nephronophthisis
 * nephronophthisis that has material basis in homozygous or compound heterozygous mutation in or deletion of the NPHP1 gene on chromosome 2q13
 * DOID:0111112
 * nephropathia epidemica
 * class of disease
 * hemorrhagic fever with renal syndrome
 * human disease
 * DOID:0050201
 * nephrosclerosis
 * class of disease
 * renal hypertension disease
 * medical condition referring to damage to the kidney due to chronic high blood pressure
 * DOID:11664
 * C12.777.419.610 C13.351.968.419.610
 * nephrosis
 * class of disease
 * proteinuria kidney disease
 * non-inflammatory kidney disease
 * DOID:2527
 * C12.777.419.630 C13.351.968.419.630
 * Nephrosis
 * nephrotic syndrome 14
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080265
 * nephrotic syndrome 15
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080271
 * nephrotic syndrome 16
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080272
 * nephrotic syndrome type 1
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13
 * DOID:0080390
 * nephrotic syndrome type 17
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25
 * DOID:0080392
 * nephrotic syndrome type 18
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42
 * DOID:0080393
 * nephrotic syndrome type 19
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in compound heterozygous mutation in the NUP160 gene on chromosome 11p11
 * DOID:0080394
 * nephrotic syndrome type 2
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease nephrotic syndrome
 * human disease
 * DOID:0080379
 * nephrotic syndrome type 20
 * class of disease
 * familial nephrotic syndrome
 * human disease
 * DOID:0070357
 * nephrotic syndrome type 22
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0112268
 * nephrotic syndrome type 3
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has material basis in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23
 * DOID:0080382
 * nephrotic syndrome type 5
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p
 * DOID:0080380
 * nephrotic syndrome type 7
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080388
 * nephrotic syndrome type 8
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25
 * DOID:0080389
 * nephrotic syndrome, type 10
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080386
 * nephrotic syndrome, type 4
 * class of disease
 * nephrotic syndrome familial nephrotic syndrome autosomal dominant disease
 * human disease
 * DOID:0080383
 * nephrotic syndrome, type 6
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080384
 * nephrotic syndrome, type 9
 * class of disease
 * familial nephrotic syndrome
 * human disease
 * DOID:0080391
 * nerve compression syndrome
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:573
 * C10.668.829.550
 * Nerve compression syndromes
 * nerve fibre bundle defect
 * class of disease
 * visual pathway disease retinal disease
 * Human disease
 * DOID:5678
 * nerve plexus neoplasm
 * class of disease
 * peripheral nervous system neoplasm plexopathy
 * Human disease
 * DOID:4693
 * nerve root neoplasm
 * class of disease
 * peripheral nervous system neoplasm radiculopathy
 * Human disease
 * DOID:4698
 * nerve sheath neoplasms
 * class of disease
 * peripheral nervous system neoplasm neoplasm
 * peripheral nervous system neoplasm that is located in the connective tissue surrounding nerves
 * DOID:3193
 * C04.557.580.600 C10.551.775.500 C10.668.829.725.500
 * nervous system benign neoplasm
 * class of disease
 * organ system benign neoplasm neurological disorder nervous system neoplasm
 * organ system benign neoplasm that is located in the central nervous system or located in the peripheral nervous system
 * DOID:0060115
 * nervous system cancer
 * class of disease
 * organ system cancer nervous system neoplasm neurological disorder
 * organ system cancer located in the nervous system that affects the central or peripheral nervous system
 * DOID:3093
 * Nervous system neoplasms
 * nervous system hibernoma
 * class of disease
 * nervous system cancer hibernoma central nervous system lipoma
 * Human disease
 * DOID:6607
 * nervous system malformations
 * class of disease
 * congenital disorder central nervous system disease neurological disorder disease
 * congenital conditions that stem from damage to, or abnormal development of, the budding nervous system
 * DOID:2490
 * C10.500 C16.131.666
 * Congenital diseases and disorders of the nervous system
 * nested variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * human disease
 * DOID:7969
 * neurilemmoma
 * class of disease
 * neuroma disease
 * benign tumor of the nerve sheat composed of Schwann cells
 * DOID:3192
 * C04.557.465.625.650.595 C04.557.580.600.610.595 C04.557.580.625.650.595
 * Schwannoma
 * Peripheral schwannoma Antoni type A (1).JPG
 * neurilemmoma of the fifth cranial nerve
 * class of disease
 * trigeminal nerve neoplasm neurilemmoma
 * Human disease
 * DOID:3202
 * neurilemmoma of the pleura
 * class of disease
 * peripheral nerve schwannoma pleural disease respiratory system benign neoplasm rare respiratory disease benign neoplasm of pleura
 * Human disease
 * DOID:6564
 * neuritis
 * class of disease symptom or sign
 * peripheral neuropathy inflammation disease
 * inflammation of a nerve or the general inflammation of the peripheral nervous system
 * DOID:1803
 * C10.668.829.650
 * Neuritis
 * neuroaxonal dystrophy
 * class of disease
 * cerebral degeneration
 * Human disease
 * DOID:2367
 * C10.228.140.744
 * neurobehavioral disorder with prenatal alcohol exposure
 * class of disease
 * fetal alcohol spectrum disorders
 * human disease
 * DOID:0081052
 * neuroblastoma
 * class of disease cancer
 * autonomic nervous system neoplasm neuroblastic tumor disease childhood cancer
 * autonomic nervous system neoplasm derived from immature nerve cells
 * DOID:769
 * C04.557.465.625.600.590.650.550 C04.557.470.670.590.650.550 C04.557.580.625.600.590.650.550
 * Neuroblastoma
 * Neuroblastoma rosettes.jpg
 * neurocirculatory asthenia
 * class of disease
 * somatoform disorder
 * somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities.
 * DOID:11569
 * F03.080.500
 * neurodegeneration
 * class of disease
 * central nervous system disease degenerative disease disease
 * central nervous system disease
 * DOID:1289
 * C10.574
 * Neurodegenerative diseases and disorders
 * [[File:Parasagittal MRI of human head in patient with benign familial macrocephaly prior to brain injury (ANIMATED).gif|center|64px]]
 * neurodegeneration with brain iron accumulation
 * class of disease
 * iron metabolism disease neurodegeneration genetic neurodegenerative disease with dementia neuroaxonal dystrophy neurometabolic disease metabolic disease with dementia miscellaneous movement disorder due to genetic neurodegenerative disease
 * neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia
 * DOID:0110734
 * neurodegeneration with brain iron accumulation 2A
 * class of disease
 * neurodegeneration with brain iron accumulation genetic disease autosomal recessive disease
 * human disease
 * DOID:0110735
 * neurodegeneration with brain iron accumulation 2B
 * class of disease
 * neurodegeneration with brain iron accumulation Infantile neuroaxonal dystrophy genetic disease autosomal recessive disease
 * human disease
 * DOID:0110736
 * neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
 * class of disease
 * nervous system heredodegenerative disease neurodegeneration autosomal recessive disease
 * hereditary disease in humans
 * DOID:0070352
 * neurodermatitis
 * class of disease symptom or sign
 * dermatitis lichen disease
 * Human disease
 * DOID:3309
 * C17.800.174.660 C17.800.815.660
 * Lichen simplex chronicus
 * Lichen simplex chronicus 1.jpg
 * neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
 * class of disease
 * syndrome neurodevelopmental disorder
 * human disease
 * DOID:0070346
 * neurodevelopmental disorder with midbrain and hindbrain malformations
 * class of disease
 * syndromic intellectual disability genetic disease autosomal recessive disease
 * human disease
 * DOID:0080312
 * neuroectodermal tumor
 * class of disease
 * tumor nervous system cancer
 * Human disease
 * DOID:171
 * C04.557.465.625 C04.557.580.625
 * neuroendocrine carcinoma
 * class of disease
 * carcinoma neuroendocrine tumor
 * carcinoma that derives from neuroendocrine cells
 * DOID:1800
 * C04.557.465.625.650.240 C04.557.470.200.025.370 C04.557.580.625.650.240
 * Large cell neuroendocrine carcinoma Case 120 (4387600323).jpg
 * neuroendocrine tumor
 * class of disease
 * endocrine gland cancer rare disease disease
 * endocrine gland cancer that has material basis in neuroendocrine cells
 * DOID:169
 * C04.557.465.625.650 C04.557.580.625.650
 * Neuroendocrine tumors
 * neurofibroma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:962
 * C04.557.580.600.580 C10.551.775.500.750 C10.668.829.725.500.600
 * Neurofibroma
 * Neurofibroma (1).jpg
 * neurofibroma of gallbladder
 * class of disease
 * neurofibroma gallbladder cancer malignant peripheral nerve neoplasm liver cancer endocrine gland cancer
 * Human disease
 * DOID:5150
 * neurofibroma of spinal cord
 * class of disease
 * neurofibroma Spinal cord cancer
 * human disease
 * DOID:13742
 * neurofibroma of the esophagus
 * class of disease
 * gastrointestinal system disease gastrointestinal system cancer esophageal cancer neurofibroma
 * Human disease
 * DOID:961
 * neurofibroma of the heart
 * class of disease
 * malignant peripheral nerve neoplasm neurofibroma
 * Human disease
 * DOID:9300
 * neurofibromatosis type I
 * class of disease
 * neurofibromatoses neuro-cardio-facial-cutaneous syndromes disease
 * type of neurofibromatosis disease
 * DOID:0111253
 * C04.557.580.600.580.590.650 C04.700.645.650 C10.562.600.500 C10.574.500.549.400 C10.668.829.675 C16.320.400.560.400 C16.320.700.645.650
 * Neurofibromatosis type 1
 * Early neurofibromatosis.jpg
 * neurofibromatosis-Noonan syndrome
 * class of disease
 * syndrome autosomal dominant disease Noonan syndrome and Noonan-related syndrome neurofibromatosis type I
 * human disease
 * DOID:0111683
 * neurofibrosarcoma
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:3512
 * C04.557.450.565.590.350.590 C04.557.450.795.350.590 C04.557.580.600.580.795 C10.551.775.500.750.750 C10.668.829.725.500.600.600
 * neurogenic arthropathy
 * class of disease
 * arthropathy disease
 * Human disease
 * DOID:14286
 * C05.550.186
 * Neuropathic arthropathy
 * neurogenic bladder
 * class of disease
 * bladder disease urination disorder disease
 * Human disease
 * DOID:12143
 * C10.597.900 C12.200.777.829.839 C12.050.351.968.829.760 C23.888.592.900 C12.950.829.760C
 * Neurogenic bladder dysfunction
 * neurogenic bowel
 * class of disease
 * intestinal disease
 * Human disease
 * DOID:13419
 * C06.405.469.158.272.804
 * neurological disorder
 * class of disease
 * disease of anatomical entity disease
 * disease of an anatomical entity located in the central or peripheral nervous system
 * DOID:0060052 DOID:863
 * C10
 * Diseases and disorders of the nervous system
 * Pyramidal hippocampal neuron 40x.jpg
 * neuroma
 * class of disease
 * nervous system benign neoplasm peripheral nervous system neoplasm tumor
 * nervous system benign neoplasm that is characterized as a nerve tissue tumor
 * DOID:2001
 * C04.557.580.600.610
 * Neuroma
 * neuromuscular disease
 * class of disease
 * peripheral neuropathy musculoskeletal disorder disease
 * neuropathy that affect the nerves that control the voluntary muscles
 * DOID:440
 * C10.668
 * Neuromuscular diseases
 * neuromuscular junction disease
 * class of disease
 * neuromuscular disease
 * neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction
 * DOID:439
 * C10.668.758
 * neuronal ceroid lipofuscinosis
 * class of disease
 * lipid storage disease eye degenerative disease nervous system heredodegenerative disease
 * Human disease
 * DOID:14503
 * C10.574.500.550 C16.320.400.600 C16.320.565.398.641.509 C18.452.584.563.641.509 C18.452.648.398.641.509
 * neuronal ceroid lipofuscinosis 1
 * class of disease
 * neuronal ceroid lipofuscinosis Infantile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease juvenile neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110721
 * neuronal ceroid lipofuscinosis 10
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease adult neuronal ceroid lipofuscinosis congenital neuronal ceroid lipofuscinosis genetic disease
 * neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15
 * DOID:0110725
 * neuronal ceroid lipofuscinosis 2
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * A condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
 * DOID:0110726
 * neuronal ceroid lipofuscinosis 3
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis genetic disease
 * A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
 * DOID:0110731
 * neuronal ceroid lipofuscinosis 4A
 * class of disease
 * neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis genetic disease Kufs disease
 * human disease
 * DOID:0110730
 * neuronal ceroid lipofuscinosis 5
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * human disease
 * DOID:0110728
 * neuronal ceroid lipofuscinosis 6
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease adult neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110729
 * neuronal ceroid lipofuscinosis 7
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * human disease
 * DOID:0110722
 * neuronal ceroid lipofuscinosis 8
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease juvenile neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110723
 * neuronal ceroid lipofuscinosis 9
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis
 * neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seziures
 * DOID:0110733
 * neuronal intestinal dysplasia
 * class of disease
 * colonic disease intestinal pseudo-obstruction intestinal dysganglionosis
 * Human disease
 * DOID:0080072
 * neuronal intestinal dysplasia type A
 * class of disease
 * neuronal intestinal dysplasia
 * human disease
 * DOID:0080679
 * neuronal intestinal dysplasia type B
 * class of disease
 * neuronal intestinal dysplasia
 * human disease
 * DOID:0080680
 * neuronitis
 * class of disease
 * central nervous system disease neurological disorder inflammatory disease disease
 * central nervous system disease that is characterized by neuron inflammation
 * DOID:8117
 * neuronopathy, distal hereditary motor, type 5B
 * class of disease
 * nervous system heredodegenerative disease distal hereditary motor neuronopathy type 5
 * human disease
 * DOID:0111205
 * neurooculocardiogenitourinary syndrome
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0111675
 * neuropathy
 * class of disease
 * neurological disorder
 * disease of or damage to the nerves
 * DOID:870
 * Neuropathies
 * neuroretinitis
 * class of disease
 * optic papillitis focal chorioretinitis eye disease
 * Human disease
 * DOID:10176
 * neurosarcoidosis
 * class of disease
 * sarcoidosis central nervous system disease
 * disease with granulomas invoving nervous tissue
 * DOID:13403
 * Neurosarcoidosis
 * neurotrophic keratoconjunctivitis
 * class of disease
 * keratoconjunctivitis
 * Human disease
 * DOID:12125
 * neutropenia
 * class of disease
 * agranulocytosis disease
 * abnormally low concentration of neutrophils in the blood
 * DOID:1227
 * C15.378.553.546.184.564 C15.378.243.750.184.564
 * Neutropenia
 * Neutropenia.JPG
 * nevoid basal cell carcinoma syndrome
 * class of disease symptom or sign
 * autosomal dominant disease syndrome
 * an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma
 * DOID:2512
 * C04.182.089.530.690.150 C04.557.470.200.165.150 C04.557.470.565.165.150 C04.700.175 C05.116.099.105 C05.500.470.690.150 C07.320.450.670.130 C16.131.077.130 C16.320.700.175
 * nickel allergic asthma
 * class of disease
 * allergic asthma nickel sensitivity metal allergy
 * allergic asthma that has allergic trigger nickel atom
 * DOID:0040045
 * night blindness
 * class of disease
 * eye disease retinal disease vision disorder disease
 * condition making it difficult or impossible to see in relatively low light
 * DOID:8499
 * C11.966.671
 * Nyctalopia
 * P360 Onderdendam goed nachtzicht ns nachtblind.jpg
 * nipple carcinoma
 * class of disease
 * breast carcinoma malignant neoplasm of nipple
 * breast carcinoma that is located in the nipple
 * DOID:6629
 * nipple duct carcinoma
 * class of disease
 * nipple carcinoma
 * nipple carcinoma that is located in the nipple duct
 * DOID:7953
 * nipple neoplasm
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:3003
 * nocturnal asthma
 * class of disease
 * chronic asthma
 * human disease
 * DOID:0080826
 * nodal marginal zone B cell lymphoma
 * class of disease
 * marginal zone B-cell lymphoma
 * marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease
 * DOID:0080211
 * nodular basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4280
 * nodular degeneration of cornea
 * class of disease
 * corneal degeneration
 * Human disease
 * DOID:2879
 * nodular episcleritis
 * class of disease
 * scleral disease episcleritis
 * Human disease
 * DOID:728
 * nodular ganglioneuroblastoma
 * class of disease
 * ganglioneuroblastoma
 * Human disease
 * DOID:5193
 * nodular goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13197
 * C19.874.283.501
 * nodular hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:2061
 * nodular medulloblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3873
 * nodular melanoma
 * class of disease
 * skin melanoma
 * melanoma that is characterized as highly aggressive and manifests as a uniform blue-black, blue-red, or amelanotic nodule
 * DOID:10047
 * Nodular melanoma
 * nodular nonsuppurative panniculitis
 * class of disease
 * panniculitis subcutaneous tissue disease
 * cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin
 * DOID:1525
 * C17.300.710.500 C17.800.566.500
 * nodular prostate
 * class of disease
 * prostatic hypertrophy
 * Human disease
 * DOID:13206
 * nodular tenosynovitis
 * class of disease
 * connective tissue benign neoplasm
 * Human disease
 * DOID:2701
 * non specific chronic endometritis
 * class of disease
 * endometritis chronic endometritis
 * Human disease
 * DOID:4560
 * non-Hodgkin lymphoma
 * class of disease
 * lymphoma neoplasm hematopoietic system disease disease
 * type of cancer of lymph nodes
 * DOID:0060060
 * C04.557.386.480 C15.604.515.569.480 C20.683.515.761.480
 * Non-Hodgkin lymphomas
 * Mantle cell lymphoma - intermed mag.jpg
 * non-Langerhans-cell histiocytosis
 * class of disease
 * histiocytosis
 * Human disease
 * DOID:4330
 * C15.604.250.410
 * non-alcoholic fatty liver
 * class of disease
 * non-alcoholic fatty liver disease
 * nonalcoholic fatty liver disease that is characterized by the presence of at least 5% of hepatic steatosis with no evidence of hepatocellular injury in the form of hepatocyte ballooning
 * DOID:0080546
 * non-alcoholic fatty liver disease
 * class of disease
 * fatty liver disease disease
 * storing of excess fat in liver cells, not caused by heavy alcohol use
 * DOID:0080208
 * C06.552.241.519
 * non-alcoholic steatohepatitis
 * class of disease
 * non-alcoholic fatty liver disease
 * Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure.
 * DOID:0080547
 * non-arteritic anterior ischemic optic neuropathy
 * class of disease
 * anterior ischemic optic neuropathy
 * Human disease
 * DOID:0050864
 * non-congenital cyst of kidney
 * class of disease
 * cystic kidney disease
 * Human disease
 * DOID:9621
 * non-controlled substance abuse
 * class of disease
 * addiction substance use disorder social issue
 * abuse of chemical substances and/or abuse of any licit substances
 * DOID:9973
 * Substance dependence
 * Toxicoman - Substance abuse.jpg
 * non-functioning pancreatic endocrine tumor
 * class of disease
 * islet cell tumor non-functioning endocrine neoplasm
 * Human disease
 * DOID:7698
 * non-gestational choriocarcinoma
 * class of disease
 * choriocarcinoma
 * Human disease
 * DOID:4320
 * C04.557.465.955.207.438 C04.557.470.200.025.455.750 C04.850.908.208.438 C13.703.720.949.208.438
 * non-gestational ovarian choriocarcinoma
 * class of disease
 * ovarian primitive germ cell tumor choriocarcinoma of ovary
 * Human disease
 * DOID:7665
 * non-invasive bladder urothelial carcinoma
 * class of disease
 * bladder urothelial carcinoma
 * human disease
 * DOID:6571
 * non-proliferative fibrocystic change of the breast
 * class of disease
 * breast fibrocystic disease
 * Human disease
 * DOID:5997
 * non-renal secondary hyperparathyroidism
 * class of disease
 * hyperparathyroidism secondary hyperparathyroidism
 * Human disease
 * DOID:13575
 * non-secretory myeloma
 * class of disease
 * multiple myeloma non-functioning endocrine neoplasm
 * Human disease
 * DOID:9547
 * non-small-cell lung carcinoma
 * class of disease
 * lung carcinoma lung cancer disease
 * any type of epithelial lung cancer other than small-cell lung carcinoma
 * DOID:3908
 * C04.588.894.797.520.109.220.249 C08.381.540.140.500 C08.785.520.100.220.500
 * Non-small cell lung cancer
 * non-suppurative otitis media
 * class of disease
 * otitis media
 * otitis media which involves transudation of fluid in the middle ear without pus formation
 * DOID:11180
 * non-syndromic X-linked intellectual disability 1
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112038
 * non-syndromic X-linked intellectual disability 100
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112040
 * non-syndromic X-linked intellectual disability 101
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112048
 * non-syndromic X-linked intellectual disability 103
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112020
 * non-syndromic X-linked intellectual disability 104
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112018
 * non-syndromic X-linked intellectual disability 105
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112036
 * non-syndromic X-linked intellectual disability 107
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112054
 * non-syndromic X-linked intellectual disability 14
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112027
 * non-syndromic X-linked intellectual disability 19
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112019
 * non-syndromic X-linked intellectual disability 2
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112016
 * non-syndromic X-linked intellectual disability 20
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112023
 * non-syndromic X-linked intellectual disability 21
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112022
 * non-syndromic X-linked intellectual disability 23
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112049
 * non-syndromic X-linked intellectual disability 30
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112051
 * non-syndromic X-linked intellectual disability 41
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112058
 * non-syndromic X-linked intellectual disability 42
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112057
 * non-syndromic X-linked intellectual disability 45
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112028
 * non-syndromic X-linked intellectual disability 46
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112055
 * non-syndromic X-linked intellectual disability 50
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112029
 * non-syndromic X-linked intellectual disability 53
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112047
 * non-syndromic X-linked intellectual disability 58
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112024
 * non-syndromic X-linked intellectual disability 63
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112050
 * non-syndromic X-linked intellectual disability 72
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112059
 * non-syndromic X-linked intellectual disability 73
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112017
 * non-syndromic X-linked intellectual disability 77
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112039
 * non-syndromic X-linked intellectual disability 81
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112033
 * non-syndromic X-linked intellectual disability 82
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112052
 * non-syndromic X-linked intellectual disability 84
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112030
 * non-syndromic X-linked intellectual disability 88
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112053
 * non-syndromic X-linked intellectual disability 89
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112031
 * non-syndromic X-linked intellectual disability 9
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112034
 * non-syndromic X-linked intellectual disability 90
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112041
 * non-syndromic X-linked intellectual disability 91
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112043
 * non-syndromic X-linked intellectual disability 92
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112032
 * non-syndromic X-linked intellectual disability 93
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112045
 * non-syndromic X-linked intellectual disability 96
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112035
 * non-syndromic X-linked intellectual disability 97
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112046
 * non-syndromic X-linked intellectual disability 98
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112044
 * non-syndromic X-linked intellectual disability 99
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112026
 * non-syndromic X-linked intellectual disability ARX-related
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112021
 * nonencapsulated sclerosing carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:5914
 * noninfectious dermatoses of eyelid
 * class of disease
 * blepharitis
 * Human disease
 * DOID:1894
 * noninvasive malignant thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:7214
 * nonossifying fibromyxoid tumor
 * class of disease
 * mesenchymal cell neoplasm fibromyxoid tumor
 * Human disease
 * DOID:8305
 * nonphotosensitive trichothiodystrophy
 * class of disease
 * trichothiodystrophy
 * human disease
 * DOID:0111867
 * nonsyndromic aplasia cutis congenita
 * class of disease
 * skin disease aplasia cutis congenita
 * human disease
 * DOID:0080661
 * nonsyndromic congenital nail disorder
 * class of disease
 * nail disease
 * human disease
 * DOID:0080683
 * nonsyndromic congenital nail disorder 1
 * class of disease
 * nail disease Twenty-nail dystrophy inherited isolated nail anomaly epidermal disease nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080079
 * nonsyndromic congenital nail disorder 2
 * class of disease
 * nail disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080080
 * nonsyndromic congenital nail disorder 5
 * class of disease
 * nail disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080083
 * nonsyndromic congenital nail disorder 6
 * class of disease
 * nail disease autosomal dominant disease nonsyndromic congenital nail disorder
 * Human disease
 * DOID:0080084
 * nonsyndromic congenital nail disorder 7
 * class of disease
 * nail disease epidermal disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080085
 * nonsyndromic congenital nail disorder 9
 * class of disease
 * nail disease inherited isolated nail anomaly autosomal recessive disease nonsyndromic congenital nail disorder
 * Human disease
 * DOID:0080087
 * nontoxic goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13195
 * normal pressure hydrocephalus
 * class of disease
 * communicating hydrocephalus nervous system heredodegenerative disease genetic dementia disease
 * condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure
 * DOID:1572
 * C10.228.140.602.750
 * Normal pressure hydrocephalus
 * normocytic anemia
 * class of disease
 * anemia
 * Human disease
 * DOID:720
 * norwegian scabies
 * class of disease
 * scabies
 * Human disease
 * DOID:14374
 * Crusted scabies
 * Norwegian Scabies in Homeless AIDS Patient.jpg
 * nose disease
 * class of disease
 * upper respiratory tract disease disease
 * respiratory disease
 * DOID:2825
 * C08.460 C09.603
 * Diseases and disorders of the nose and paranasal sinuses
 * notochordal cancer
 * class of disease
 * bone cancer
 * embryonal cancer and bone cancer and mesenchymal cell neoplasm that is located in the notochord
 * DOID:3303
 * nuclear senile cataract
 * class of disease
 * senile cataract nuclear sclerosis
 * Human disease
 * DOID:13963
 * nuclear type mitochondrial complex I deficiency
 * class of disease
 * mitochondrial complex I deficiency
 * human disease
 * DOID:0112065
 * nuclear type mitochondrial complex I deficiency 1
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112074
 * nuclear type mitochondrial complex I deficiency 10
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112075
 * nuclear type mitochondrial complex I deficiency 11
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112089
 * nuclear type mitochondrial complex I deficiency 12
 * class of disease
 * nuclear type mitochondrial complex I deficiency X-linked recessive disease
 * human disease
 * DOID:0112099
 * nuclear type mitochondrial complex I deficiency 13
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112076
 * nuclear type mitochondrial complex I deficiency 14
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112094
 * nuclear type mitochondrial complex I deficiency 15
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112077
 * nuclear type mitochondrial complex I deficiency 16
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112096
 * nuclear type mitochondrial complex I deficiency 17
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112078
 * nuclear type mitochondrial complex I deficiency 18
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112070
 * nuclear type mitochondrial complex I deficiency 19
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112085
 * nuclear type mitochondrial complex I deficiency 2
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112083
 * nuclear type mitochondrial complex I deficiency 20
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112072
 * nuclear type mitochondrial complex I deficiency 21
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112088
 * nuclear type mitochondrial complex I deficiency 22
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112069
 * nuclear type mitochondrial complex I deficiency 23
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112087
 * nuclear type mitochondrial complex I deficiency 24
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112079
 * nuclear type mitochondrial complex I deficiency 25
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112067
 * nuclear type mitochondrial complex I deficiency 26
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112086
 * nuclear type mitochondrial complex I deficiency 27
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112090
 * nuclear type mitochondrial complex I deficiency 28
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112095
 * nuclear type mitochondrial complex I deficiency 29
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112084
 * nuclear type mitochondrial complex I deficiency 3
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112093
 * nuclear type mitochondrial complex I deficiency 30
 * class of disease
 * nuclear type mitochondrial complex I deficiency X-linked recessive disease
 * human disease
 * DOID:0112098
 * nuclear type mitochondrial complex I deficiency 31
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112071
 * nuclear type mitochondrial complex I deficiency 32
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112080
 * nuclear type mitochondrial complex I deficiency 33
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112097
 * nuclear type mitochondrial complex I deficiency 34
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112091
 * nuclear type mitochondrial complex I deficiency 35
 * class of disease
 * autosomal recessive disease mitochondrial complex I deficiency nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112139
 * nuclear type mitochondrial complex I deficiency 4
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112082
 * nuclear type mitochondrial complex I deficiency 5
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112068
 * nuclear type mitochondrial complex I deficiency 6
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112066
 * nuclear type mitochondrial complex I deficiency 7
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112092
 * nuclear type mitochondrial complex I deficiency 8
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112081
 * nuclear type mitochondrial complex I deficiency 9
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112073
 * null-cell leukemia
 * class of disease
 * acute lymphocytic leukemia
 * Human disease
 * DOID:9954
 * nutmeg liver
 * class of disease
 * hepatic vascular disease
 * human disease
 * DOID:13739
 * Congestive hepatopathy
 * nutrition disorder
 * class of disease
 * acquired metabolic disease nutritional and metabolic diseases food-related disease
 * disease that results from excessive or inadequate intake of food and nutrients
 * DOID:374
 * C18.654
 * Nutritional diseases and disorders
 * nutritional deficiency disease
 * class of disease
 * nutrition disorder deficiency
 * human disease
 * DOID:5113
 * C18.654.521.500
 * Diseases and disorders due to nutritional deficiencies
 * nutritional optic neuropathy
 * class of disease
 * optic nerve disease optic neuritis
 * Human disease
 * DOID:1209
 * nystagmus, congenital, autosomal recessive
 * class of disease
 * congenital nystagmus autosomal recessive disease
 * human disease
 * DOID:0111797
 * obsessive-compulsive disorder
 * class of disease
 * anxiety disorder impulse control disorder genetic nervous system disorder genetic disease disease
 * anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)
 * DOID:10933
 * F03.080.600
 * Obsessive–compulsive disorder
 * Obsessive-compulsive disorder world map - DALY - WHO2002.svg
 * obsessive-compulsive personality disorder
 * class of disease
 * personality disorder disease
 * personal perfectionism at the cost of flexibility, openness, efficiency & effect on others
 * DOID:10932
 * F03.675.150
 * Obsessive compulsive personality disorder
 * obstructive hydrocephalus
 * class of disease
 * hydrocephalus
 * abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of an obstruction at any location within the ventricular system that prevents cerebrospinal fluid flowing into the subarachnoid space
 * DOID:14159
 * obstructive jaundice
 * class of disease
 * cholestasis jaundice non-neoplastic bile duct disorder
 * Human disease
 * DOID:13603
 * C23.550.429.500.755 C23.888.885.375.500
 * Obstructive jaundice
 * obstructive lung disease
 * class of disease
 * lung disease disease
 * category of respiratory disease characterized by airway obstruction
 * DOID:2320
 * C08.381.495
 * obstructive nephropathy
 * class of disease
 * kidney disease
 * kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction
 * DOID:0070314
 * obstructive sleep apnea
 * class of disease
 * sleep apnea
 * obstruction of the upper airway during sleep
 * DOID:0050848
 * C08.618.085.852.850 C10.886.425.800.750.850
 * occipital lobe neoplasm
 * class of disease
 * cerebrum cancer
 * Human disease
 * DOID:910
 * occlusion of gallbladder
 * class of disease
 * gallbladder disease
 * Human disease
 * DOID:9714
 * occlusion precerebral artery
 * class of disease
 * cerebrovascular disease
 * human disease
 * DOID:5976
 * occupational asthma
 * class of disease
 * occupational disease asthma environmental induced asthma
 * medical condition caused or exacerbated by the workplace
 * DOID:0080820
 * C08.127.108.495 C08.674.095.495 C20.543.480.680.095.495 C24.102
 * occupational dermatitis
 * class of disease
 * contact dermatitis occupational disease disease
 * Human disease
 * DOID:4404
 * C17.800.174.255.700 C17.800.815.255.700 C24.270
 * ochronosis
 * class of disease
 * connective tissue disease clinical sign disease
 * syndrome caused by the accumulation of homogentisic acid in connective tissues
 * DOID:14223
 * C23.550.744
 * Ochronosis
 * Homogentisic acid.svg
 * ocular albinism
 * class of disease
 * eye disease albinism disease
 * human disease
 * DOID:0050633
 * C11.270.040.090 C16.320.290.040.090 C16.320.565.100.102.090 C16.320.850.080.090 C17.800.621.440.102.090 C17.800.827.080.090 C18.452.648.100.102.090
 * ocular albinism type 2
 * class of disease
 * ocular albinism eye disease X-linked recessive disease
 * Human disease
 * DOID:0050630
 * ocular albinism with sensorineural deafness
 * class of disease
 * ocular albinism Waardenburg's syndrome autosomal dominant disease digenic disease
 * human disease
 * DOID:0090100
 * ocular cancer
 * class of disease
 * sensory system cancer eye tumor eye disease disease
 * type of cancer un the eye
 * DOID:2174
 * ocular hyperemia
 * class of disease
 * conjunctival disease
 * Human disease
 * DOID:1248
 * ocular hypertension
 * class of disease
 * eye disease hypertension disease
 * eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss
 * DOID:9282
 * C11.525
 * ocular hypotension
 * class of disease
 * eye disease hypotension
 * Human disease
 * DOID:790
 * C11.540
 * ocular motility disease
 * class of disease
 * cranial nerve disease eye adnexa disease eye disease
 * human disease
 * DOID:1279
 * C10.228.758 C10.292.562 C11.590
 * ocular tuberculosis
 * class of disease
 * extrapulmonary tuberculosis eye disease tuberculosis
 * Human disease
 * DOID:233 DOID:0070344
 * C01.150.252.289.800 C01.375.354.800 C11.294.354.800
 * oculocutaneous albinism type 2
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13
 * DOID:0070096
 * oculocutaneous albinism type 3
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of TYRP1 on chromosome 9p23
 * DOID:0070097
 * oculocutaneous albinism type 4
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.
 * DOID:0070098
 * oculocutaneous albinism type IA
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.
 * DOID:0070094
 * oculocutaneous albinism type IB
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.
 * DOID:0070095
 * oculocutaneous albinism type V
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA5 on chromosome 4q24
 * DOID:0070099
 * oculoglandular tularemia
 * class of disease
 * tularemia
 * tularemia that results in inflammation of eye and swelling of lymph glands in front of the ear
 * DOID:13226
 * oculogyric crisis
 * class of disease
 * focal dystonia disease
 * focal dystonia that is characterized by a prolonged involuntary upward deviation of the eyes
 * DOID:0050842
 * oculomotor nerve paralysis
 * class of disease
 * third cranial nerve disease paralytic squint
 * Human disease
 * DOID:11550
 * C10.292.562.700 C11.590.436
 * Oculomotor nerve palsy
 * oculopharyngodistal myopathy 4
 * class of disease
 * Oculopharyngodistal myopathy
 * human disease
 * DOID:0081300
 * odontoclasia
 * class of disease
 * dental caries
 * Human disease
 * DOID:11736
 * olecranon bursitis
 * class of disease
 * enthesopathy bursitis disease
 * Human disease
 * DOID:12581
 * Olecranon bursitis
 * Bursitis Elbow WC.JPG
 * olfactory groove meningioma
 * class of disease
 * anterior cranial fossa meningioma
 * Human disease
 * DOID:8057
 * olfactory nerve disease
 * class of disease
 * glossopharyngeal nerve disease encephalopathy
 * Human disease
 * DOID:367
 * C10.292.650
 * oligoasthenoteratospermia
 * class of disease
 * oligospermia Teratospermia asthenozoospermia male infertility
 * A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.
 * DOID:0070311
 * oligodendroglioma
 * class of disease
 * glioma disease
 * type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell
 * DOID:3181
 * C04.557.465.625.600.380.590 C04.557.470.670.380.590 C04.557.580.625.600.380.590
 * Oligodendrogliomas
 * Oligodendroglioma1 high mag.jpg
 * oligohydramnios
 * class of disease
 * placenta disease disease
 * placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion
 * DOID:12215
 * C13.703.560
 * Oligohydramnios
 * oligospermia
 * class of disease
 * male infertility disease
 * semen with abnormally low concentration of sperm
 * DOID:14228
 * C12.294.365.700.508
 * Oligospermia
 * olivopontocerebellar atrophy
 * class of disease
 * neurodegeneration
 * group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives
 * DOID:14784
 * C10.177.575.550.375 C10.228.140.079.612.600 C10.228.140.252.700.650 C10.228.662.550.600 C10.228.854.787.750 C10.574.500.825.650 C10.574.625.600 C16.320.400.780.750
 * omphalocele
 * class of disease
 * congenital disorder abdominal wall defect disease
 * physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac
 * DOID:0060327
 * Omphalocele
 * oncocytic breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:6585
 * oophoritis
 * class of disease symptom or sign
 * ovarian disease inflammatory disease disease
 * human disease
 * DOID:10974
 * C13.351.500.056.630.450 C13.351.500.056.750.500 C19.391.630.450
 * open-angle glaucoma
 * class of disease
 * glaucoma
 * glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage
 * DOID:1067
 * C11.525.381.407
 * ophthalmia neonatorum
 * class of disease
 * gonococcal eye infectious disease bacterial conjunctivitis
 * Human disease
 * DOID:9699
 * ophthalmia nodosa
 * class of disease
 * eye disease
 * Human disease
 * DOID:9722
 * ophthalmomyiasis
 * class of disease
 * myiasis eye disease parasitic eye infection
 * myiasis that involves parasitic infestation of Oestrus ovis larvae in the eye causing severe irritation, edema, and pain
 * DOID:0050268
 * ophthalmoplegia
 * class of disease symptom or sign
 * ocular motility disease paralysis disease
 * Human disease
 * DOID:539
 * C10.292.562.750 C10.597.622.447 C11.590.472 C23.888.592.636.447
 * Ophthalmoparesis
 * opiate dependence
 * class of disease
 * substance dependence opioid use disorder
 * drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance
 * DOID:2559
 * opioid use disorder
 * class of disease
 * addiction substance abuse opioid-related disorders disease
 * substance abuse disorder that involves the recurring use of opioid drugs despite negative consequences
 * DOID:11206
 * Opioid use disorder
 * opportunistic bacterial infectious disease
 * class of disease
 * bacterial infectious disease opportunistic infection
 * bacterial infectious disease that results in infection by bacteria in individuals whose host defense mechanisms have been compromised
 * DOID:0050340
 * opportunistic mycosis
 * class of disease
 * systemic mycosis opportunistic infection
 * A systemic mycosis that results in fungal infection located in human body of immunocompromised individuals, has material basis in Fungi. The organisms invade via the respiratory tract, alimentary tract, or intravascular devices.
 * DOID:2473
 * oppositional defiant disorder
 * class of disease
 * specific developmental disorder emotional and behavioral disorders disease
 * human disorder involving hostility and defiance
 * DOID:0050856
 * F03.625.094.475
 * Oppositional defiant disorder
 * optic atrophy 10
 * class of disease
 * autosomal dominant disease optic atrophy
 * human disease
 * DOID:0111434
 * optic atrophy 11
 * class of disease
 * autosomal recessive isolated optic atrophy autosomal recessive disease optic atrophy
 * human disease
 * DOID:0111436
 * optic atrophy 2
 * class of disease
 * optic atrophy
 * human disease
 * DOID:0111443
 * optic atrophy 4
 * class of disease
 * Kjer's optic neuropathy optic atrophy autosomal dominant disease
 * human disease
 * DOID:0111440
 * optic atrophy 5
 * class of disease
 * Kjer's optic neuropathy optic atrophy autosomal dominant disease
 * human disease
 * DOID:0111438
 * optic atrophy 6
 * class of disease
 * autosomal recessive isolated optic atrophy optic atrophy autosomal recessive disease
 * human disease
 * DOID:0111435
 * optic atrophy 9
 * class of disease
 * autosomal recessive disease optic atrophy
 * human disease
 * DOID:0111442
 * optic disk drusen
 * class of disease
 * optic nerve disease
 * Human disease
 * DOID:13561
 * C10.292.700.450 C11.640.513
 * optic nerve astrocytoma
 * class of disease
 * optic nerve glioma optic nerve disease astrocytoma neuromuscular disease
 * human disease
 * DOID:4991
 * optic nerve disease
 * class of disease
 * cranial nerve disease vision disorder peripheral neuropathy visual pathway disease neuro-ophthalmological disease disease
 * cranial nerve disease that is located in the optic nerve
 * DOID:1891
 * C10.292.700 C11.640
 * Optic neuropathy
 * optic nerve glioma
 * class of disease
 * optic nerve tumor glioma visual pathway glioma brain glioma
 * human disease
 * DOID:4992
 * C04.557.465.625.600.380.795 C04.557.470.670.380.795 C04.557.580.625.600.380.795 C04.588.614.300.600.600 C04.588.614.596.240.240.500 C10.292.225.800.500 C10.292.700.500.500 C10.551.360.500.500 C10.551.775.250.500.500 C11.640.544.500
 * optic neuritis
 * class of disease
 * optic nerve disease eye disease encephalomyelitis disease
 * optic nerve disease that results in inflammation located in optic nerve which may cause a complete or partial loss of vision
 * DOID:1210
 * C10.292.700.550 C11.640.576
 * Optic neuritis
 * optic papillitis
 * class of disease
 * optic neuritis
 * human disease
 * DOID:10175
 * oral cavity carcinoma in situ
 * class of disease
 * in situ carcinoma mouth cancer mouth disease carcinoma in situ of digestive organ
 * Human disease
 * DOID:0050610
 * oral hairy leukoplakia
 * class of disease
 * mouth disease oral mucosa leukoplakia disease
 * mouth disease characterized by a white patch on the lateral sides of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus
 * DOID:0060315
 * C01.925.256.466.313.500 C04.588.443.591.545.500 C04.834.512.513.500 C07.465.565.545.500 C23.300.816.513.500
 * oral leukoedema
 * class of disease
 * mouth disease Leukoedema
 * Human disease
 * DOID:4557
 * C07.465.385
 * oral mucosa leukoplakia
 * class of disease
 * mouth disease leukoplakia
 * Human disease
 * DOID:9655
 * C04.588.443.591.545 C04.834.512.513 C07.465.565.545 C23.300.816.513
 * Oral leukoplakia
 * oral submucous fibrosis
 * class of disease
 * mouth disease rare maxillo-facial surgical disease
 * human disease
 * DOID:5773
 * C07.465.654
 * oral-facial-digital syndrome
 * class of disease
 * syndrome
 * genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene
 * DOID:4501
 * C05.116.099.370.652 C05.660.207.700 C16.131.077.676 C16.131.260.830.670 C16.131.621.207.700 C16.320.180.830.670 C16.320.714
 * orange allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Citrus sinensis plant fruit food product.
 * DOID:0060508
 * orbit embryonal rhabdomyosarcoma
 * class of disease
 * orbit rhabdomyosarcoma embryonal rhabdomyosarcoma
 * Human disease
 * DOID:3258
 * orbit rhabdomyosarcoma
 * class of disease
 * orbit sarcoma
 * Human disease
 * DOID:3259
 * orbital cancer
 * class of disease
 * bone cancer orbit neoplasm orbital disease
 * Human disease
 * DOID:4143
 * orbital cyst
 * class of disease
 * orbital disease
 * Human disease
 * DOID:14233
 * orbital disease
 * class of disease
 * eye adnexa disease bone disease
 * adnexa disease that is located in the eye socket
 * DOID:930
 * C11.675
 * orbital granuloma
 * class of disease
 * chronic orbital inflammation
 * Human disease
 * DOID:10499
 * orbital osteomyelitis
 * class of disease
 * acute orbital inflammation osteomyelitis
 * Human disease
 * DOID:11232
 * orbital periostitis
 * class of disease
 * acute orbital inflammation
 * human disease
 * DOID:11231
 * orbital tenonitis
 * class of disease
 * acute orbital inflammation
 * Human disease
 * DOID:11233
 * orchitis
 * class of disease
 * testicular disease inflammatory disease disease
 * inflammation of the testes
 * DOID:2518
 * C12.294.829.493 C19.391.829.493
 * Orchitis
 * Orkite cok2 pere polets 32 samwinnes.JPG
 * organ system benign neoplasm
 * class of disease
 * benign neoplasm disease of anatomical entity
 * benign neoplasm that is classified by the organ system from which it is arising from
 * DOID:0060085
 * organ system cancer
 * class of disease
 * cancer cancer by anatomical entity
 * cancer that is classified based on the organ it starts in
 * DOID:0050686
 * C04.588
 * organic acidemia
 * class of disease
 * amino acid metabolic disorder
 * amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids
 * DOID:0060159
 * orofacial cleft 1
 * class of disease
 * cleft lip and cleft palate autosomal dominant disease
 * An orofacial cleft characterized by autosomal dominant inheritance that has material basis in variation in chromosome region 6p24.3.
 * DOID:0080395
 * orofacial cleft 10
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in mutation in the SUMO1 gene on chromosome 2q33
 * DOID:0080403
 * orofacial cleft 11
 * class of disease
 * cleft lip and cleft palate
 * human disease
 * DOID:0080404
 * orofacial cleft 12
 * class of disease
 * cleft lip and cleft palate
 * An orofacial cleft that has material basis in variation in the chromosome region 8q24.3.
 * DOID:0080405
 * orofacial cleft 13
 * class of disease
 * cleft lip and cleft palate autosomal dominant disease
 * orofacial cleft characterized by autosomal doninant inhertitance that has material basis in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730
 * DOID:0080406
 * orofacial cleft 14
 * class of disease
 * cleft lip and cleft palate autosomal recessive disease
 * human disease
 * DOID:0080407
 * orofacial cleft 15
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in mutation in the DLX4 gene on chromosome 17q21
 * DOID:0080408
 * orofacial cleft 2
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the chromosome region 2p13
 * DOID:0080396
 * orofacial cleft 3
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the chromosomal region 19q13
 * DOID:0080397
 * orofacial cleft 4
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the 4q21-q31 chromosomal region
 * DOID:0080398
 * orofacial cleft 5
 * class of disease
 * cleft lip and cleft palate
 * human disease
 * DOID:0080399
 * orofacial cleft 6
 * class of disease
 * autosomal dominant disease cleft lip and cleft palate
 * human disease
 * DOID:0080593
 * orofacial cleft 7
 * class of disease
 * cleft lip and cleft palate autosomal recessive disease
 * orofacial cleft that has material basis in by homozygous mutation in the PVRL1 gene on chromosome 11q23
 * DOID:0080400
 * orofacial cleft 8
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in heterozygous mutation in the TP63 gene on chromosome 3q28
 * DOID:0080401
 * orofacial cleft 9
 * class of disease
 * cleft lip and cleft palate
 * An orofacial cleft that has material basis in variation in the chromosome region 13q33.1-q34.
 * DOID:0080402
 * orofaciodigital syndrome VIII
 * class of disease
 * oral-facial-digital syndrome X-linked recessive disease
 * human disease
 * DOID:0060378
 * oromandibular dystonia
 * class of disease
 * focal dystonia lingual-facial-buccal dyskinesia focal, segmental or multifocal dystonia
 * focal dystonia that is characterized by distortions of the mouth and tongue.
 * DOID:0050843
 * oropharyngeal anthrax
 * class of disease
 * gastrointestinal anthrax
 * human disease
 * DOID:0050059
 * orthostatic proteinuria
 * class of disease symptom or sign
 * kidney disease proteinuria
 * Human disease
 * DOID:9617
 * osmotic diarrhea
 * class of disease
 * diarrhea chronic diarrhea
 * Human disease
 * DOID:0050130
 * ossifying fibroma
 * class of disease
 * bone benign neoplasm
 * bone benign neoplasm that is located in the mouth and results in an overgrowth of gingival tissue due to irritation or trauma
 * DOID:180
 * C04.557.450.565.575.400 C04.557.450.565.590.340.360
 * ossifying fibromyxoid tumour
 * class of disease
 * fibromyxoid tumor mesenchymal cell neoplasm
 * human disease
 * DOID:2685
 * osteoarticular tuberculosis
 * class of disease
 * extrapulmonary tuberculosis bone disease
 * extrapulmonary tuberculosis that results in formation of lesions located in bone
 * DOID:1639
 * C01.150.252.410.040.552.846.617.525 C01.160.886 C05.116.165.886
 * osteoblastoma
 * class of disease
 * bone benign neoplasm osteogenic neoplasm disease
 * Human disease
 * DOID:0060098
 * C04.557.450.565.575.600
 * Osteoblastoma
 * Osteoblastoma - high mag.jpg
 * osteochondrodysplasia
 * class of disease
 * bone development disease
 * bone development disease that results in defective development of cartilage or bone
 * DOID:2256
 * C05.116.099.708 C16.320.728
 * Osteochondrodysplasias
 * osteochondrosis
 * class of disease symptom or sign
 * ischemic bone disease disease
 * ischemic bone disease that results in necrosis followed by regrowth in children and teens located in bone
 * DOID:8125
 * C05.116.821
 * Osteochondrosis
 * osteoclast-like giant cell neoplasm of the pancreas
 * class of disease
 * pancreatic ductal adenocarcinoma undifferentiated pancreatic carcinoma
 * Human disease
 * DOID:7718
 * osteogenesis imperfecta 21
 * class of disease
 * osteogenesis imperfecta
 * human disease
 * DOID:0112201
 * osteogenesis imperfecta type 1
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by bone fragility and blue sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110334
 * osteogenesis imperfecta type 16
 * class of disease
 * osteogenesis imperfecta
 * osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
 * DOID:0110345
 * osteogenesis imperfecta type 18
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111848
 * osteogenesis imperfecta type 20
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111849
 * osteogenesis imperfecta type 3
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has material basis in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110339
 * osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
 * class of disease
 * osteogenesis imperfecta dentinogenesis imperfecta blue sclera
 * osteogenesis imperfecta found in a single South African family
 * DOID:0110335
 * osteomalacia
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone
 * DOID:10573
 * C05.116.198.816.640 C18.452.104.816.640 C18.452.174.845.640 C18.654.521.500.133.770.734.640
 * Calcitriol.svg
 * osteomyelitis
 * class of disease
 * bone inflammation disease infectious disease disease
 * bone inflammation disease that has material basis in infection located in bone or located in bone marrow
 * DOID:1019
 * C01.160.495 C05.116.165.495
 * Osteomyelitis
 * osteonecrosis
 * class of disease symptom or sign
 * necrosis ischemic bone disease disease
 * bone death caused when the bone no longer receives blood supply
 * DOID:10159
 * C05.116.852 C23.550.717.732
 * Aseptic osteonecrosis
 * Head of femur avascular necrosis.jpg
 * osteopoikilosis
 * class of disease
 * osteosclerosis
 * osteosclerosis that results in numerous bone islands located in skeleton
 * DOID:11991
 * C05.116.099.708.702.685 C17.300.705
 * Osteopoikilosis
 * osteoporosis
 * class of disease
 * bone resorption disease disease
 * bone resorption disease characterized by the thinning of bone tissue and decreased mechanical strength
 * DOID:11476
 * C05.116.198.579 C18.452.104.579
 * Osteoporosis
 * Osteoporosis -- Smart-Servier.jpg
 * osteosarcoma
 * class of disease
 * bone cancer cell type cancer bone sarcoma osteogenic neoplasm disease childhood cancer
 * bone cancer that is located in bone that has material basis in cells of mesenchymal origin
 * DOID:3347
 * C04.557.450.565.575.650 C04.557.450.795.620
 * Osteosarcoma
 * Osteosarcoma.jpg
 * osteosarcoma arising in bone Paget's disease
 * class of disease
 * bone osteosarcoma mammary Paget's disease
 * Human disease
 * DOID:7542
 * osteosclerosis
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that results in abnormal elevated bone density or mass
 * DOID:4254
 * C05.116.099.708.702
 * ScleroticmetastaticdiseasePelvis.png
 * otomycosis
 * class of disease symptom or sign
 * otitis externa dermatomycosis disease
 * human disease
 * DOID:0050147
 * C01.150.703.658 C09.218.736
 * Otomycosis
 * Otomycosis.jpg
 * otopalatodigital syndrome spectrum disorder
 * class of disease
 * bone development disease
 * DOID:0111782
 * otosclerosis
 * class of disease
 * inner ear disease disease
 * otitis interna characterized by an abnormal bone growth in the middle ear
 * DOID:12185
 * C09.218.768
 * Otosclerosis
 * Gray919.png
 * otospondylomegaepiphyseal dysplasia, autosomal dominant
 * class of disease
 * osteochondrodysplasia autosomal dominant disease
 * human disease
 * DOID:0080677
 * outlet dysfunction constipation
 * class of disease
 * constipation
 * Human disease
 * DOID:2088
 * ovarian Brenner tumor
 * class of disease
 * ovarian benign neoplasm
 * ovarian benign neoplasm that has material basis in the surface epithelium of the ovary
 * DOID:2636
 * Brenner tumour
 * ovarian Wilms' cancer
 * class of disease
 * ovarian cancer
 * malignant neoplasm of ovary and nephroblastoma that is located in the ovaries
 * DOID:2153
 * ovarian angiosarcoma
 * class of disease
 * angiosarcoma ovary sarcoma sarcoma ovarian cancer
 * human disease
 * DOID:4527
 * ovarian benign neoplasm
 * class of disease
 * female reproductive organ benign neoplasm ovarian neoplasm endocrine organ benign neoplasm ovarian disease
 * human disease
 * DOID:0060112
 * Benign neoplasms of the ovary
 * ovarian biphasic or triphasic teratoma
 * class of disease
 * ovarian germ cell teratoma
 * Human disease
 * DOID:6232
 * ovarian cancer
 * class of disease
 * female reproductive organ cancer ovarian neoplasm ovarian disease endocrine gland cancer rare genetic endocrine disease inherited gynecological tumor disease
 * female reproductive organ cancer that is located in the ovary
 * DOID:2394
 * Ovarian cancer
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian carcinoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinoma
 * human disease
 * DOID:4001
 * ovarian carcinosarcoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinosarcoma mixed Müllerian tumor
 * Human disease
 * DOID:6170
 * ovarian clear cell adenocarcinoma
 * class of disease
 * ovary adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5304
 * ovarian clear cell adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5897
 * ovarian clear cell cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma ovarian clear cell adenocarcinoma
 * Human disease
 * DOID:7438
 * ovarian clear cell cystadenofibroma
 * class of disease
 * ovarian clear cell adenofibroma clear cell cystadenofibroma
 * Human disease
 * DOID:5896
 * ovarian clear cell malignant adenofibroma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:6554
 * ovarian cyst
 * class of disease
 * ovarian disease ovarian neoplasm disease
 * fluid-filled sac in the ovary
 * DOID:5119
 * C04.182.612 C13.351.500.056.630.580 C19.391.630.580
 * Ovarian cysts
 * Benign Ovarian Cyst.jpg
 * ovarian cystadenocarcinoma
 * class of disease
 * ovary adenocarcinoma cystadenocarcinoma ovarian cystadenoma
 * human disease
 * DOID:3605
 * ovarian cystadenoma
 * class of disease
 * ovarian benign neoplasm benign epithelial neoplasm
 * human disease
 * DOID:3269
 * ovarian cystic teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:5118
 * Mature cystic teratoma of ovary
 * ovarian disease
 * class of disease
 * female reproductive system disease gonadal disease adnexal disease
 * Human disease
 * DOID:1100
 * C13.351.500.056.630 C19.391.630
 * Diseases and disorders of ovaries
 * ovarian dysfunction
 * class of disease
 * ovarian disease
 * Human disease
 * DOID:1414
 * ovarian dysgenesis 1
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16
 * DOID:0080493
 * ovarian dysgenesis 4
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MCM9 gene on chromosome 6q22
 * DOID:0080496
 * ovarian dysgenesis 5
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the SOHLH1 gene on chromosome 9q34
 * DOID:0080497
 * ovarian dysgenesis 6
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the NUP107 gene on chromosome 12q15
 * DOID:0080498
 * ovarian dysgenesis 7
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MRPS22 gene on chromosome 3q23
 * DOID:0080499
 * ovarian dysgenesis 8
 * class of disease
 * 46 XX gonadal dysgenesis autosomal dominant disease
 * 46 XX gonadal dysgenesis that has material basis in heterozygous mutation in the ESR2 gene on chromosome 14q23
 * DOID:0080500
 * ovarian embryonal carcinoma
 * class of disease
 * embryonal carcinoma malignant non-dysgerminomatous germ cell tumor of ovary ovarian cancer
 * embryonal carcinoma that is located in the ovary
 * DOID:5681
 * ovarian endodermal sinus tumor
 * class of disease
 * ovarian primitive germ cell tumor malignant non-dysgerminomatous germ cell tumor of ovary endodermal sinus tumor
 * Human disease
 * DOID:5350
 * ovarian endometrial cancer
 * class of disease
 * surface epithelial-stromal tumor Endometrioid tumor female reproductive endometrioid cancer
 * ovary epithelial cancer that has material basis in the endometrium and is located in the ovary
 * DOID:6212
 * ovarian endometrioid adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5480
 * ovarian endometrioid cystadenofibroma
 * class of disease
 * ovarian endometrioid adenofibroma cystadenofibroma
 * Human disease
 * DOID:7411
 * ovarian endometrioid cystadenoma
 * class of disease
 * ovarian cystadenoma
 * Human disease
 * DOID:7191
 * ovarian endometrioid malignant adenofibroma
 * class of disease
 * ovarian carcinosarcoma malignant adenofibroma
 * Human disease
 * DOID:6445
 * ovarian endometrioid stromal sarcoma
 * class of disease
 * ovary sarcoma
 * Human disease
 * DOID:5169
 * ovarian fetiform teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6314
 * ovarian germ cell monodermal and highly specialized teratoma
 * class of disease
 * monodermal teratoma
 * Human disease
 * DOID:2641
 * ovarian germ cell neoplasm
 * class of disease
 * ovarian neoplasm germ cell tumor germ cell and embryonal neoplasms ovarian cancer
 * benign or malignant ovarian tumor that originates in the germ (egg) cells of the ovary
 * DOID:2156
 * Germ cell neoplasms
 * ovarian germ cell teratoma
 * class of disease
 * ovarian germ cell neoplasm teratoma gonadal teratoma female reproductive organ cancer
 * Human disease
 * DOID:5567
 * Ovarian teratomas
 * Teratoma Ovary 4x.jpg
 * ovarian gonadoblastoma
 * class of disease
 * ovarian benign neoplasm gonadoblastoma
 * Human disease
 * DOID:3578
 * ovarian large-cell neuroendocrine carcinoma
 * class of disease
 * ovarian carcinoma familiar ovarian carcinoma inherited neuroendocrine tumor large cell neuroendocrine carcinoma
 * Human disease
 * DOID:4555
 * ovarian lymphoma
 * class of disease
 * ovarian cancer lymphoma
 * Human disease
 * DOID:2150
 * ovarian malignant mesothelioma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:2143
 * ovarian melanoma
 * class of disease
 * ovarian cancer
 * ovarian cancer that has material basis in melanoctyes
 * DOID:0050928
 * ovarian mesodermal adenosarcoma
 * class of disease
 * ovarian carcinosarcoma adenosarcoma
 * adenosarcoma and malignant ovarian endometroid tumorthat is located in the ovary
 * DOID:4115
 * ovarian mixed germ cell neoplasm
 * class of disease
 * ovarian primitive germ cell tumor mixed germ cell cancer
 * Human disease
 * DOID:5936
 * ovarian mucinous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma malignant ovarian mucinous tumor mucinous adenocarcinoma
 * human disease
 * DOID:3606
 * ovarian mucinous adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * human disease
 * DOID:6469
 * ovarian mucinous cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma mucinous cystadenocarcinoma ovarian mucinous adenocarcinoma
 * Human disease
 * DOID:3604
 * ovarian mucinous cystadenofibroma
 * class of disease
 * ovarian mucinous adenofibroma mucinous cystadenofibroma
 * Human disease
 * DOID:7013
 * ovarian mucinous malignant adenofibroma
 * class of disease
 * malignant ovarian mucinous tumor malignant adenofibroma ovarian mucinous neoplasm
 * Human disease
 * DOID:6278
 * ovarian mucinous neoplasm
 * class of disease
 * surface epithelial-stromal tumor mucinous tumor
 * Human disease
 * DOID:6067
 * Ovarian mucinous tumors
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian papillary cystadenoma
 * class of disease
 * ovarian papillary neoplasm papillary adenoma ovarian cystadenoma
 * Human disease
 * DOID:6405
 * ovarian papillary neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:6214
 * ovarian primitive germ cell tumor
 * class of disease
 * malignant ovarian germ cell neoplasm
 * Human disease
 * DOID:5351
 * ovarian serous adenofibroma
 * class of disease
 * ovarian benign neoplasm serous adenofibroma
 * Human disease
 * DOID:5474
 * ovarian serous carcinoma
 * class of disease
 * ovarian carcinoma serous carcinoma ovarian serous tumor
 * ovarian carcinoma that has material basis in the lining of the ovary and produces a serum-like fluid
 * DOID:0050933
 * Ovarian serous carcinoma
 * ovarian serous cystadenofibroma
 * class of disease
 * ovarian serous adenofibroma cystadenofibroma
 * Human disease
 * DOID:7320
 * ovarian serous cystadenoma
 * class of disease
 * serous cystadenoma ovarian benign neoplasm ovarian cystadenocarcinoma serous cystadenocarcinoma ovarian cystadenoma ovarian serous tumor
 * ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed
 * DOID:5746 DOID:3914
 * C04.557.470.035.320.240 C04.557.470.590.485.240
 * Ovarian serous cystadenoma
 * Ovarian serous cystadenoma - alt -- low mag.jpg
 * ovarian sex cord-stromal tumor
 * class of disease
 * sex cord-gonadal stromal tumor
 * A benign or malignant neoplasm that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts. Representative examples include thecoma, fibroma, Sertoli cell tumor, and granulosa cell tumor.
 * DOID:0080369
 * ovarian small cell carcinoma
 * class of disease
 * ovarian carcinoma small cell carcinoma
 * Human disease
 * DOID:6179
 * ovarian solid teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6315
 * ovarian squamous cell carcinoma
 * class of disease
 * ovarian squamous cell neoplasm squamous cell carcinoma ovarian cancer
 * Human disease
 * DOID:5531
 * ovarian squamous cell neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:5532
 * ovarian surface papilloma
 * class of disease
 * ovarian papillary neoplasm
 * Human disease
 * DOID:6407
 * ovary adenocarcinoma
 * class of disease
 * ovarian carcinoma adenocarcinoma
 * ovarian carcinoma that derives from epithelial cells of glandular origin
 * DOID:3713
 * Adenocarcinomas of the ovary
 * [[File:Metastatic ovarian adenocarcinoma- Pleural fluid cell block Case 168 (5494503444).jpg|center|64px]]
 * ovary leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5263
 * ovary mixed epithelial carcinoma
 * class of disease
 * ovarian carcinoma
 * Human disease
 * DOID:6898 DOID:6899
 * ovary neuroendocrine neoplasm
 * class of disease
 * ovarian cancer neuroendocrine tumor
 * Human disease
 * DOID:3002
 * ovary papillary carcinoma
 * class of disease
 * ovarian papillary neoplasm ovarian carcinoma
 * Human disease
 * DOID:6408
 * ovary rhabdomyosarcoma
 * class of disease
 * ovary sarcoma rhabdomyosarcoma
 * Human disease
 * DOID:4059
 * ovary sarcoma
 * class of disease
 * ovarian cancer sarcoma
 * human disease
 * DOID:2146
 * ovary serous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma ovarian serous carcinoma
 * ovary adenocarcinoma that derives from the lining of a cavity that produces a serum-like fluid (a serous cavity)
 * DOID:5744
 * Serous adenocarcinoma of the ovary
 * overhydrated hereditary stomatocytosis
 * class of disease
 * macrocytic anemia autosomal dominant disease hereditary stomatocytosis
 * human disease
 * DOID:0111562
 * overnutrition
 * class of disease
 * nutrition disorder malnutrition
 * form of malnutrition in which the intake of nutrients is oversupplied
 * DOID:654
 * C18.654.726
 * ovine and caprine brucellosis
 * class of disease
 * brucellosis
 * A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.
 * DOID:14456
 * oxirane allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger oxirane
 * DOID:0040082
 * oxyphilic adenoma
 * class of disease
 * endocrine organ benign neoplasm oncocytic neoplasm benign epithelial neoplasm disease
 * Human disease
 * DOID:5389
 * C04.557.470.035.140
 * Oncocytoma
 * Parotid gland oncocytoma - very high mag.jpg
 * oxyphilic endometrial endometrioid adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:6865
 * pain agnosia
 * class of disease
 * agnosia absence of pain sensation
 * agnosia that is a loss of the ability to perceive and process pain
 * DOID:0060145
 * pain disorder
 * class of disease
 * somatoform disorder disease pain
 * somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.
 * DOID:0060164
 * palindromic rheumatism
 * class of disease
 * syndrome arthritis
 * human disease
 * DOID:1166
 * palladium allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis metal allergy
 * allergic contact dermatitis that has allergic trigger palladium
 * DOID:0040055
 * palmoplantar keratosis
 * class of disease
 * keratosis foot diseases epidermal disease disease
 * keratosis characterized by abnormal thickening of the palms and the soles
 * DOID:3390
 * C16.320.850.475 C17.800.428.435 C17.800.827.475
 * Palmoplantar keratodermas
 * pancreas disease
 * class of disease
 * endocrine system disease
 * endocrine system disease that is located in the pancreas
 * DOID:26
 * C06.689
 * Diseases and disorders of pancreas
 * pancreas lymphoma
 * class of disease
 * pancreatic cancer lymphoma
 * human disease
 * DOID:1792
 * pancreas sarcoma
 * class of disease
 * pancreatic cancer sarcoma
 * pancreatic cancer that is located in the pancreas and that arises from transformed cells of mesenchymal origin
 * DOID:1796
 * pancreatic ACTH hormone producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:7697
 * pancreatic acinar cell adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma Acinar cell carcinoma of the pancreas acinar adenocarcinoma
 * pancreatic adenocarcinoma that has material basis in cells with morphological resemblance to acinar cells and is associated with increased serum lipase
 * DOID:5742
 * pancreatic adenocarcinoma
 * class of disease
 * pancreatic carcinoma adenocarcinoma
 * pancreatic carcinoma that derives from epithelial cells of glandular origin
 * DOID:4074
 * Adenocarcinomas of the pancreas
 * [[File:Metastatic pancreatic adenocarcinoma with lepidic growth pattern Case 280 (9840005374).jpg|center|64px]]
 * pancreatic cancer
 * class of disease
 * endocrine gland cancer pancreas disease pancreatic neoplasm gastrointestinal system cancer disease
 * endocrine gland cancer located in the pancreas
 * DOID:1793
 * Pancreatic cancer
 * MBq cystic-carcinoma-pancreas.jpg
 * pancreatic carcinoma
 * class of disease
 * pancreatic cancer carcinoma gastrointestinal carcinoma
 * pancreas cancer that derives from epithelial cells located in the pancreas
 * DOID:4905
 * pancreatic cholera
 * class of disease
 * endocrine pancreas disease
 * Human disease
 * DOID:6977
 * pancreatic colloid cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma mucinous cystadenocarcinoma
 * Human disease
 * DOID:7234
 * pancreatic cystadenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma cystadenocarcinoma
 * Human disease
 * DOID:4073
 * pancreatic cystadenoma
 * class of disease
 * benign neoplasm of exocrine pancreas endocrine organ benign neoplasm benign neoplasm of pancreas gastrointestinal system benign neoplasm pancreas disease
 * human disease
 * DOID:3918
 * pancreatic delta cell neoplasm
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:4433
 * pancreatic ductal adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * pancreatic adenocarcinoma that derives from pancreatic duct cells
 * DOID:3498
 * pancreatic ductal carcinoma
 * class of disease
 * pancreatic cancer ductal carcinoma pancreatic carcinoma
 * most common cancer of the pancreas
 * DOID:3587
 * C04.557.470.200.025.232.750 C04.557.470.615.132.750 C04.588.274.761.750 C04.588.322.475.750 C06.301.761.750 C06.689.667.625 C19.344.421.750
 * pancreatic foamy gland adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * Human disease
 * DOID:7577
 * pancreatic gastrinoma
 * class of disease
 * islet cell tumor functional pancreatic neuroendocrine tumor
 * Human disease
 * DOID:5580
 * pancreatic intraductal papillary-colloid carcinoma
 * class of disease
 * pancreatic adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7574
 * pancreatic intraductal papillary-mucinous adenoma
 * class of disease
 * pancreatic intraductal papillary-mucinous neoplasm adenoma of pancreas gastrointestinal system benign neoplasm adenoma
 * Human disease
 * DOID:7851
 * pancreatic intraductal papillary-mucinous neoplasm
 * class of disease
 * cancer of exocrine pancreas
 * Human disease
 * DOID:7575
 * pancreatic invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma
 * Human disease
 * DOID:8150
 * pancreatic invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * Human disease
 * DOID:7236
 * pancreatic mucinous cystadenoma
 * class of disease
 * mucinous cystadenoma pancreatic cystadenoma
 * human disease
 * DOID:7235
 * pancreatic mucinous ductal ectasia
 * class of disease
 * pancreas disease
 * Human disease
 * DOID:13313
 * pancreatic non-functioning delta cell tumor
 * class of disease
 * pancreatic delta cell neoplasm non-functioning pancreatic endocrine tumor
 * Human disease
 * DOID:7840
 * pancreatic non-invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7685
 * pancreatic non-invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * human disease
 * DOID:7237
 * pancreatic serous cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma serous cystadenocarcinoma pancreatic serous cystic neoplasm
 * Human disease
 * DOID:5751
 * pancreatic serous cystadenoma
 * class of disease
 * serous cystadenoma pancreatic cystadenoma disease
 * human disease
 * DOID:3917
 * Serous cystadenoma pancreas
 * pancreatic serous cystic neoplasm
 * class of disease
 * pancreatic exocrine neoplasm Serous tumour cystic lesions of the pancreas cancer of exocrine pancreas
 * Human disease
 * DOID:3919
 * Serous cystic neoplasms of the pancreas
 * pancreatic signet ring cell adenocarcinoma
 * class of disease
 * pancreatic ductal adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:3497
 * pancreatic solid pseudopapillary carcinoma
 * class of disease
 * pancreatic carcinoma
 * pancreatic carcinoma that is characterized by its papillary architecture
 * DOID:6827
 * pancreatic somatostatinoma
 * class of disease
 * islet cell tumor pancreatic delta cell neoplasm somatostatinoma
 * Human disease
 * DOID:4432
 * pancreatic squamous cell carcinoma
 * class of disease
 * pancreatic cancer squamous cell carcinoma
 * squamous cell carcinoma located in the pancreas
 * DOID:0080323
 * pancreatic steatorrhea
 * class of disease
 * pancreas disease steatorrhea
 * Human disease
 * DOID:10610
 * pancreatic vasoactive intestinal peptide producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:5741
 * pancreatoblastoma
 * class of disease
 * pancreatic carcinoma rare epithelial tumor of pancreas disease
 * Human disease
 * DOID:6823
 * pancytopenia
 * class of disease
 * anemia cytopenia disease
 * medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets
 * DOID:12450
 * C15.378.243.875
 * panhypopituitarism, X-linked
 * class of disease
 * panhypopituitarism X-linked disease
 * human disease
 * DOID:0111779
 * panic disorder
 * class of disease
 * anxiety disorder disease
 * anxiety disorder characterized by reoccurring unexpected panic attacks
 * DOID:594
 * F03.080.700
 * Panic disorder
 * Panic attack.jpg
 * panniculitis
 * class of disease
 * fibromyalgia connective tissue disease skin disease disease
 * Inflammation of the subcutaneous adipose tissue
 * DOID:1526
 * C17.300.710 C17.800.566
 * Panniculitis
 * An introduction to dermatology (1905) erythema induratum 2.jpg
 * panuveitis
 * class of disease
 * uveitis
 * Human disease
 * DOID:12030
 * C11.941.879.780
 * papillary adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue
 * DOID:3112
 * C04.557.470.200.025.085
 * papillary adenofibroma
 * class of disease
 * adenofibroma
 * biphasic polypoid neoplasm characterized by the presence of papillary projections that are lined by epithelial cells and fibrotic stroma
 * DOID:5479
 * papillary adenoma
 * class of disease
 * glandular cell epithelial neoplasm adenoma
 * Human disease
 * DOID:3172
 * papillary carcinoma
 * class of disease
 * carcinoma
 * carcinoma derived from epithelial cells with finger-like projections
 * DOID:3113
 * C04.557.470.200.360 C04.557.470.700.360
 * papillary conjunctivitis
 * class of disease
 * conjunctivitis
 * Human disease
 * DOID:2458
 * papillary craniopharyngioma
 * class of disease
 * craniopharyngioma
 * Human disease
 * DOID:3847
 * papillary cystadenocarcinoma
 * class of disease
 * cystadenocarcinoma papillary cystic tumor
 * cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with cysts and papillary endophytic projections
 * DOID:3110
 * C04.557.470.200.025.480.230 C04.557.470.590.480.230
 * papillary eccrine adenoma
 * class of disease
 * eccrine sweat gland neoplasm papillary adenoma
 * Human disease
 * DOID:5446
 * papillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5505
 * papillary extrahepatic bile duct adenocarcinoma
 * class of disease
 * extrahepatic bile duct adenocarcinoma
 * Human disease
 * DOID:6931
 * papillary follicular thyroid adenocarcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:3968
 * C04.557.470.200.025.060.225 C04.557.470.200.025.085.225
 * papillary hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:5439
 * Papillary hidradenoma
 * Papillary hidradenoma - very high mag.jpg
 * papillary meningioma of the cerebellum
 * class of disease
 * cerebellum cancer rhabdoid meningioma papillary meningioma brain meningioma
 * Human disease
 * DOID:5057
 * papillary pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8193
 * papillary renal cell carcinomas
 * class of disease
 * renal cell carcinoma
 * renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors
 * DOID:4465
 * [[File:Histopathology of papillary renal cell carcinoma type 1, grade 2, with variable density.jpg|center|64px]]
 * papillary serous adenocarcinoma
 * class of disease
 * papillary adenocarcinoma
 * papillary adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures with psammoma bodies
 * DOID:2632
 * papillary squamous carcinoma
 * class of disease
 * squamous cell carcinoma papillary carcinoma
 * Human disease
 * DOID:4385
 * papillary thymic adenocarcinoma
 * class of disease
 * thymus adenocarcinoma
 * Human disease
 * DOID:5595
 * papillary thyroid cancer
 * class of disease
 * thyroid carcinoma papillary carcinoma differentiated thyroid carcinoma
 * thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer
 * DOID:3969
 * C04.557.470.200.025.085.612 C04.588.322.894.400 C04.588.443.915.400 C19.344.894.400 C19.874.788.400
 * Thyroid papillary carcinoma
 * papillary transitional carcinoma
 * class of disease
 * transitional cell carcinoma
 * transitional cell carcinoma that has several papillary fronds with central fibrovascular core lined by transitional type epithelium
 * DOID:4012
 * Urothelial papillary carcinoma
 * papillary urothelial neoplasm of low malignant potential
 * class of disease
 * bladder papillary transitional cell neoplasm urinary tract non-invasive transitional cell neoplasm papillary urothelial lesion
 * human disease
 * DOID:6239
 * papilledema
 * class of disease
 * optic nerve disease disease
 * Human disease
 * DOID:146
 * C10.292.700.900 C11.640.710
 * Papilledema
 * Papilledema.jpg
 * papilloma
 * class of disease
 * benign neoplasms by histologic type papillary tumor disease
 * cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue
 * DOID:2615
 * C04.557.470.700.600
 * Papillomas
 * parachordoma
 * class of disease
 * mesenchymal cell neoplasm
 * Human disease
 * DOID:2647
 * paralytic ileus
 * class of disease
 * bowel obstruction ileus
 * Human disease
 * DOID:8442
 * Paralytic ileus
 * paralytic lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:12958
 * paralytic poliomyelitis
 * class of disease
 * poliomyelitis central nervous system disease
 * Human disease
 * DOID:0050515
 * paralytic squint
 * class of disease
 * strabismus cranial nerve palsy
 * Human disease
 * DOID:10863
 * parameningeal embryonal rhabdomyosarcoma
 * class of disease
 * embryonal rhabdomyosarcoma
 * embryonal rhabdomyosarcoma located in the parameningeal region
 * DOID:0060338
 * parametritis
 * class of disease
 * pelvic inflammatory diseases inflammatory disease uterine disease
 * Human disease
 * DOID:1260
 * C13.351.500.056.750.750
 * parametrium malignant neoplasm
 * class of disease
 * uterine adnexa cancer broad ligament malignant neoplasm
 * Human disease
 * DOID:11746
 * paramyotonia congenita of Von Eulenburg
 * class of disease
 * neuromuscular disease autosomal dominant disease paramyotonia congenita
 * human disease
 * DOID:0111538
 * paranasal sinus disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:1352
 * C08.460.692 C09.603.692
 * paranasal sinus lymphoma
 * class of disease
 * paranasal sinus cancer lymphoma
 * human disease
 * DOID:1355
 * paranasal sinus neoplasm
 * class of disease
 * respiratory tract neoplasm paranasal sinus disease respiratory system benign neoplasm
 * human disease
 * DOID:1350
 * C04.588.443.665.650.693 C08.460.669.693 C08.460.692.503 C08.785.600.693 C09.603.669.693 C09.603.692.503 C09.647.685.693
 * Neoplasms of paranasal sinuses
 * paranasal sinus sarcoma
 * class of disease
 * paranasal sinus cancer sarcoma
 * sarcoma and malignant tumor of nasal sinuses that is located in the paranasal sinus
 * DOID:1362
 * paraneoplastic pemphigus
 * class of disease
 * pemphigus
 * human disease
 * DOID:0080852
 * paraneoplastic polyneuropathy
 * class of disease
 * inflammatory and toxic neuropathy peripheral neuropathy paraneoplastic neurologic syndrome
 * Human disease
 * DOID:8681
 * C04.588.614.550.700 C04.730.856.700 C10.574.781.850 C10.668.829.800.662
 * paranoid personality disorder
 * class of disease
 * personality disorder disease
 * mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others
 * DOID:10938
 * F03.675.600
 * Paranoid personality disorder
 * parapharyngeal meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:8216
 * paraphilia
 * class of disease
 * psychosexual disorder sexual and gender disorder disease
 * experience of intense sexual arousal to atypical objects, situations, or individuals
 * DOID:0060044
 * F03.657
 * Paraphilias
 * Martin van Maele - La Comtesse au fouet 01.jpg
 * paraphimosis
 * class of disease
 * phimosis disease
 * medical condition in which the foreskin of a penis becomes trapped behind the glans penis
 * DOID:5334
 * C12.294.494.684.587
 * Paraphimosis
 * Paraphimosis.jpg
 * paraplegia
 * class of disease symptom or sign
 * central nervous system disease paralysis disease
 * impairment in motor or sensory function of the lower extremities
 * DOID:607
 * C10.597.622.669 C23.888.592.636.637
 * Paraplegia
 * parapsoriasis
 * class of disease
 * psoriasis disease
 * Human disease
 * DOID:9088
 * C17.800.859.575
 * parasagittal meningioma
 * class of disease
 * cerebral convexity meningioma
 * Human disease
 * DOID:6869
 * parasitic Ichthyosporea infectious disease
 * class of disease
 * parasitic infectious diseases
 * parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals
 * DOID:0050291
 * C03.600
 * parasitic conjunctivitis
 * class of disease
 * chronic conjunctivitis parasitic eye infection
 * Human disease
 * DOID:13341
 * parasitic eyelid infestation
 * class of disease
 * blepharitis parasitic eye infection
 * Human disease
 * DOID:13823
 * parasitic protozoa infectious disease
 * class of disease
 * parasitic infectious diseases disease
 * parasitic disease caused by a protozoan
 * DOID:2789
 * C01.610.752
 * paratesticular lipoma
 * class of disease
 * reproductive organ benign neoplasm lipoma
 * Human disease
 * DOID:10207
 * parathyroid adenoma
 * class of disease
 * parathyroid neoplasm benign parathyroid gland neoplasm benign neoplasms by histologic type adenoma disease
 * Human disease
 * DOID:7608
 * Parathyroid adenoma
 * parathyroid gland disease
 * class of disease
 * endocrine system disease
 * endocrine disease
 * DOID:11201
 * C19.642
 * parathyroid oncocytic adenoma
 * class of disease
 * parathyroid adenoma oxyphilic adenoma
 * Human disease
 * DOID:7611
 * parathyroid transitional clear cell adenoma
 * class of disease
 * parathyroid adenoma
 * Human disease
 * DOID:7609
 * paraurethral gland cancer
 * class of disease
 * female reproductive organ cancer paraurethral gland neoplasm
 * Human disease
 * DOID:14059
 * paraurethral gland neoplasm
 * class of disease
 * urethral benign neoplasm
 * Human disease
 * DOID:2139
 * parenchymatous neurosyphilis
 * class of disease
 * tertiary neurosyphilis
 * Human disease
 * DOID:0050490
 * parietal lobe ependymoma
 * class of disease
 * parietal lobe malignant neoplasm ependymoma
 * parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain
 * DOID:0050903
 * paronychia
 * class of disease
 * nail disease disease
 * bacterial or fungal nail infection of the hand or foot
 * DOID:13117
 * C01.539.800.460 C17.800.529.639 C17.800.838.486
 * Paronychia (disease)
 * Paronychia.jpg
 * parotid disease
 * class of disease
 * salivary gland disease
 * Human disease
 * DOID:10302
 * C07.465.815.470
 * Diseases and disorders of parotid glands
 * parotitis
 * class of disease
 * parotid disease inflammatory disease sialadenitis disease
 * parotid disease characterized by the inflammation of one or both parotid glands
 * DOID:10301
 * C07.465.815.470.800 C07.465.815.793.500
 * parovarian cyst
 * class of disease
 * female reproductive system disease embryonic cyst of fallopian tube
 * Human disease
 * DOID:4333
 * C04.182.668 C23.300.306.500
 * paroxysmal nonkinesigenic dyskinesia 2
 * class of disease
 * Paroxysmal dyskinesia dystonia genetic disease
 * human disease
 * DOID:0090047
 * pars planitis
 * class of disease
 * intermediate uveitis chorioretinitis ciliary body disease rare genetic eye disease disease
 * Human disease
 * DOID:12731
 * C11.941.160.478.700 C11.941.879.780.900.300.659 C11.941.879.900.500
 * parthenolide allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger parthenolide
 * DOID:0040072
 * partial androgen insensitivity syndrome
 * class of disease
 * X-linked recessive disease androgen insensitivity syndrome
 * medical condition
 * DOID:0080776
 * partial arterial retinal occlusion
 * class of disease
 * retinal artery occlusion
 * Human disease
 * DOID:14522
 * partial circumpapillary choroid dystrophy
 * class of disease
 * hereditary choroidal atrophy
 * human disease
 * DOID:9811
 * partial lipodystrophy
 * class of disease
 * lipodystrophy
 * lipodystrophy that is characterized by partial loss of adipose tissue
 * DOID:0080299
 * partial motor epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3327
 * C10.228.140.490.360.272
 * partial optic atrophy
 * class of disease
 * optic atrophy
 * human disease
 * DOID:10631
 * partial pancreatic agenesis
 * class of disease
 * pancreas disease agenesis pancreatic agenesis
 * pancreas disease that is characterized by the failure of the pancreas to develop prior to birth
 * DOID:0050877
 * partial retinal vein occlusion
 * class of disease
 * retinal vein occlusion
 * Human disease
 * DOID:1726
 * partial sensory epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3330
 * C10.228.140.490.360.275
 * partial third-nerve palsy
 * class of disease
 * paralytic squint oculomotor nerve paralysis
 * Human disease
 * DOID:10864
 * patellar tendinitis
 * class of disease
 * tendinitis knee disorder knee extensor tendonitis
 * Human disease
 * DOID:10471
 * Patellar tendinitis
 * patent blue V allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger patent blue V
 * DOID:0040080
 * paternal uniparental disomy of chromosome 14
 * class of disease
 * uniparental disomy of paternal origin uniparental disomy 14 syndrome
 * human disease
 * DOID:0111712
 * pathologic nystagmus
 * class of disease
 * nystagmus ocular motility disease abnormal eye movements
 * Human disease
 * DOID:9650
 * C10.292.562.675 C11.590.400
 * patterned macular dystrophy 1
 * class of disease
 * patterned macular dystrophy
 * human disease
 * DOID:0060866
 * patulous eustachian tube
 * class of disease physiological condition
 * eustachian tube disease
 * eustachian tube disorder
 * DOID:12358
 * peach allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus persica plant fruit food product.
 * DOID:0060510
 * peanut allergy
 * class of disease
 * tree nut allergy legume allergy vegetable allergy
 * type of food allergy caused by peanuts
 * DOID:4378
 * C20.543.480.370.572.750
 * Nut warning 1.jpg
 * pediatric CNS choriocarcinoma
 * class of disease
 * malignant childhood germ cell neoplasm central nervous system choriocarcinoma rare childhood malignant neoplasm choriocarcinoma
 * Human disease
 * DOID:6639
 * pediatric CNS embryonal cell carcinoma
 * class of disease
 * central nervous system childhood germ cell tumor central nervous system embryonal carcinoma rare childhood malignant neoplasm malignant childhood germ cell neoplasm brain cancer
 * Human disease
 * DOID:7231
 * pediatric angiosarcoma
 * class of disease
 * angiosarcoma rare childhood malignant neoplasm
 * angiosarcoma that affects children
 * DOID:4505
 * pediatric cerebral ependymoblastoma
 * class of disease
 * ependymoblastoma
 * Human disease
 * DOID:7841
 * pediatric ependymoma
 * class of disease
 * ependymoma childhood cancer ependymal tumor childhood neoplasm
 * human disease
 * DOID:5509
 * pediatric epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7095
 * pediatric fibrosarcoma
 * class of disease
 * fibrosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3520
 * pediatric germ cell tumor
 * class of disease
 * germ cell tumor childhood neoplasm
 * Human disease
 * DOID:6053
 * pediatric hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma childhood cancer of liver
 * Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age
 * DOID:0070322
 * pediatric infratentorial ependymoblastoma
 * class of disease
 * childhood infratentorial neoplasm ependymoblastoma infratentorial cancer childhood central nervous system primitive neuroectodermal neoplasm rare childhood malignant neoplasm
 * Human disease
 * DOID:7522
 * pediatric infratentorial ependymoma
 * class of disease
 * infratentorial cancer pediatric ependymoma brain ependymoma childhood infratentorial neoplasm childhood cancer
 * Human disease
 * DOID:7501
 * pediatric leptomeningeal melanoma
 * class of disease
 * meningeal melanoma
 * Human disease
 * DOID:6089
 * pediatric liposarcoma
 * class of disease
 * liposarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5695
 * pediatric low-grade glioma
 * class of disease
 * low grade glioma
 * human disease
 * DOID:0080830
 * pediatric lymphoma
 * class of disease
 * lymphoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5823
 * pediatric meningioma
 * class of disease
 * meningioma pediatric central nervous system tumor
 * Human disease
 * DOID:4593
 * pediatric mesenchymal chondrosarcoma
 * class of disease
 * mesenchymal chondrosarcoma childhood cancer
 * Human disease
 * DOID:4546
 * pediatric myxoid chondrosarcoma
 * class of disease
 * myxoid chondrosarcoma childhood cancer
 * Human disease
 * DOID:6494
 * pediatric osteosarcoma
 * class of disease
 * osteosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3361
 * pediatric ovarian dysgerminoma
 * class of disease
 * pediatric ovarian germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm dysgerminoma of ovary
 * dysgerminoma of ovary that occurs in children
 * DOID:7340
 * pediatric ovarian germ cell tumor
 * class of disease
 * ovarian germ cell neoplasm pediatric germ cell tumor
 * Human disease
 * DOID:6084
 * pediatric supratentorial ependymoma
 * class of disease
 * supratentorial cancer pediatric ependymoma brain ependymoma
 * Human disease
 * DOID:7502
 * pediatric testicular germ cell tumor
 * class of disease
 * testicular germ cell tumor pediatric germ cell tumor
 * Human disease
 * DOID:6082
 * peliosis hepatis
 * class of disease
 * hepatic vascular disease
 * Human disease
 * DOID:914
 * C06.552.802
 * Peliosis hepatis
 * pellagra
 * class of disease
 * nutritional deficiency disease other acquired skin disease skin disease disease
 * Human disease
 * DOID:8457
 * C18.654.521.500.133.699.529
 * Pellagra
 * Pellagra NIH.jpg
 * pelvic inflammatory diseases
 * class of disease
 * female reproductive system disease adnexal disease infectious disease disease
 * infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis
 * DOID:1003
 * C01.635.500 C12.050.351.500.056.750 C12.100.250.056.750
 * Pelvic inflammatory disease
 * Blausen 0732 PID-Sites.png
 * pelvic lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3927
 * pelvic muscle wasting
 * class of disease
 * pelvic organ prolapse pelvic floor dysfunction
 * Human disease
 * DOID:11629
 * pelvic organ prolapse
 * class of disease
 * female reproductive system disease prolapse
 * pelvic organs protruding from the opening of the vagina
 * DOID:1284
 * C23.300.842.624
 * Female genital prolapse
 * Hippocrates treatment for prolapse.png
 * pelvic varices
 * class of disease
 * varicose veins
 * Human disease
 * DOID:9742
 * pemphigoid
 * class of disease
 * autoimmune skin disease bullous skin disease
 * human disease
 * DOID:0080841
 * penicillin drug reaction
 * class of disease
 * adverse drug reaction beta-lactam allergy Side effects of penicillin
 * beta-lactam allergy triggered by penicillin
 * DOID:0060520
 * penicilliosis
 * class of disease
 * opportunistic mycosis disease
 * Human disease
 * DOID:0050288
 * penile cancer
 * class of disease
 * penile neoplasm male reproductive organ cancer penile disease disease
 * cancer of the penis
 * DOID:11615
 * Penile cancer
 * Penile cancer 2.jpg
 * penile disease
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:1529
 * C12.294.494
 * penile neoplasm
 * class of disease
 * male reproductive system neoplasm penile disease male reproductive organ benign neoplasm
 * human disease
 * DOID:11624
 * C04.588.945.440.715 C12.294.260.500 C12.294.494.591 C12.758.409.500
 * Penile neoplasms
 * penile urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8223
 * penis Paget's disease
 * class of disease
 * penis carcinoma extramammary Paget's disease adenocarcinoma of penis genetic urogenital tumor
 * Human disease
 * DOID:3448
 * Penile Paget's disease
 * penis basal cell carcinoma
 * class of disease
 * penis carcinoma basal-cell carcinoma rare skin disease
 * human disease
 * DOID:4277
 * penis basaloid carcinoma
 * class of disease
 * penis squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7047
 * penis carcinoma
 * class of disease
 * penile cancer carcinoma
 * penile cancer that is located in the skin or tissues of the penis
 * DOID:3449
 * penis carcinoma in situ
 * class of disease
 * in situ carcinoma penile disease penis squamous cell carcinoma carcinoma in situ of male genital organs
 * Human disease
 * DOID:8872
 * penis mixed squamous cell carcinoma
 * class of disease
 * penis squamous cell carcinoma
 * Human disease
 * DOID:8009
 * penis non-invasive verrucous carcinoma
 * class of disease
 * penis verrucous carcinoma penis carcinoma in situ cervical verrucous carcinoma
 * Human disease
 * DOID:5907
 * penis papillary carcinoma
 * class of disease
 * penis squamous cell carcinoma papillary squamous carcinoma
 * Human disease
 * DOID:8013
 * penis sarcoma
 * class of disease
 * penile cancer sarcoma
 * sarcoma and malignant neoplasm of penis that is located in the penis
 * DOID:11838
 * penis squamous cell carcinoma
 * class of disease
 * penis carcinoma squamous cell carcinoma
 * penis carcinoma that has material basis in squamous cells
 * DOID:5518
 * Squamous-cell carcinoma of the penis
 * penis verrucous carcinoma
 * class of disease
 * penis squamous cell carcinoma verrucous carcinoma penis papillary carcinoma
 * Human disease
 * DOID:5908
 * peptic esophagitis
 * class of disease
 * peptic ulcer disease esophagitis gastroesophageal reflux disease
 * human disease
 * DOID:13976
 * C06.405.117.620.420 C06.405.205.663.420 C06.405.469.275.800.523 C06.405.748.586.524
 * peptic ulcer disease
 * class of disease
 * gastrointestinal system disease duodenal disease disease
 * ulcer of an area of the gastrointestinal tract
 * DOID:750
 * C06.405.469.275.800 C06.405.748.586
 * Peptic ulcers
 * Benign gastric ulcer 1.jpg
 * perforated corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10445
 * perforated ulcer
 * class of disease
 * peptic ulcer disease gastric perforation
 * medical condition of the gastrointestinal tract wall
 * DOID:752
 * C06.405.469.275.800.698 C06.405.748.586.698
 * DU 2.jpg
 * perforation of bile duct
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:13409
 * periampullary adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma
 * Human disease
 * DOID:8110
 * periampullary adenoma
 * class of disease
 * ampulla of Vater neoplasm adenoma
 * Human disease
 * DOID:0050849
 * perianal gland tumor
 * class of disease
 * cancer in dogs anus neoplasm
 * dog disease
 * DOID:4550
 * C04.588.083 C04.588.274.476.411.307.790.040.040 C06.301.371.411.307.790.040.040 C06.405.249.411.307.790.040.040 C06.405.469.491.307.790.040.040 C06.405.469.860.101.163.083 C06.405.469.860.180.500.040.040 C22.073
 * perianal hematoma
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9745
 * Perianal hematoma
 * perianal skin Paget's disease
 * class of disease
 * anal margin carcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:7708
 * periapical abscess
 * class of disease
 * periapical periodontitis dental abscess
 * localized collection of pus associated with a tooth
 * DOID:2562
 * C01.539.830.025.650 C07.320.830.700.700 C07.465.714.306.700.700 C07.465.714.533.487.700
 * periapical periodontitis
 * class of disease
 * inflammation periodontitis dental pulp disease periapical disease tooth pathology
 * Human disease
 * DOID:823
 * C07.320.830.700 C07.465.714.306.700 C07.465.714.533.487
 * pericardial effusion
 * class of disease symptom or sign
 * pericardium disease cardiovascular system symptom disease
 * pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
 * DOID:118
 * C14.280.695
 * Pericardial effusion
 * pericardial mesothelioma
 * class of disease
 * pericardium cancer mesothelioma
 * Human disease
 * DOID:6201
 * pericarditis
 * class of disease
 * pericardium disease inflammation inflammatory disease heart disease disease
 * pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
 * DOID:1787
 * C14.280.720
 * Pericarditis
 * Pericarditis10.JPG
 * pericardium cancer
 * class of disease
 * heart cancer neoplasm of pericardium pericardium disease
 * Human disease
 * DOID:116
 * pericardium leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of pericardium pericardium disease cardiovascular organ benign neoplasm
 * Human disease
 * DOID:5137
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * class of disease
 * cystadenofibroma
 * benign neoplasm characterized by the presence of cystic structures lined by mucinous columnar epithelial cells in a fibrotic stroma
 * DOID:6468
 * mucinous intrahepatic cholangiocarcinoma
 * class of disease
 * intrahepatic cholangiocarcinoma bile duct mucinous adenocarcinoma
 * Human disease
 * DOID:7024
 * mucinous lung adenocarcinoma
 * class of disease
 * adenocarcinoma of the lung mucinous adenocarcinoma
 * lung adenocarcinoma with tumor cells floating in pools of mucin that distend alveolar spaces
 * DOID:0080303
 * mucinous ovarian cystadenoma
 * class of disease
 * ovarian cystadenoma mucinous cystadenoma
 * Human disease
 * DOID:3267
 * Mucinous cystoadenoma of the ovary
 * Mucinous Cystadenoma of Ovary (218889489).jpg
 * mucinous pancreas adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma mucinous adenocarcinoma
 * human disease
 * DOID:0080782
 * mucinous stomach adenocarcinoma
 * class of disease
 * gastric diffuse adenocarcinoma mucinous adenocarcinoma
 * Human disease
 * DOID:3716
 * mucinous tubular and spindle cell carcinoma
 * class of disease
 * renal cell carcinoma tubulopathy spindle cell carcinoma
 * human disease
 * DOID:4472
 * Mucinous tubular and spindle cell carcinoma
 * Renal Mucinous spindle 1.JPG
 * mucocele of appendix
 * class of disease
 * intestinal disease mucocele
 * Human disease
 * DOID:13248
 * mucoepidermoid esophageal carcinoma
 * class of disease
 * esophageal carcinoma mucoepidermoid carcinoma
 * Human disease
 * DOID:4686
 * mucoepidermoid thyroid carcinoma
 * class of disease
 * thyroid carcinoma mucoepidermoid carcinoma thyroid gland adenocarcinoma
 * Human disease
 * DOID:4687
 * mucolipidosis type III gamma
 * class of disease
 * pseudo-Hurler polydystrophy mucolipidosis autosomal recessive disease
 * human disease
 * DOID:0080678
 * mucopolysaccharidosis IV
 * class of disease
 * human disease
 * DOID:0050808
 * mucopolysaccharidosis Ih
 * class of disease
 * autosomal recessive disease mucopolysaccharidosis I
 * human disease
 * DOID:0111390
 * mucopolysaccharidosis Ih/s
 * class of disease
 * autosomal recessive disease mucopolysaccharidosis I
 * human disease
 * DOID:0111389
 * mucopolysaccharidosis type IIIA
 * class of disease
 * Sanfilippo syndrome autosomal recessive disease
 * human disease
 * DOID:0111395
 * mucopolysaccharidosis type IIIB
 * class of disease
 * Sanfilippo syndrome autosomal recessive disease
 * human disease
 * DOID:0111394
 * mucopolysaccharidosis type IIIC
 * class of disease
 * autosomal recessive disease Sanfilippo syndrome
 * human disease
 * DOID:0111393
 * mucopolysaccharidosis type IIID
 * class of disease
 * autosomal recessive disease Sanfilippo syndrome
 * human disease
 * DOID:0111402
 * mucopolysaccharidosis type IVA
 * class of disease
 * Morquio syndrome autosomal recessive disease
 * human disease
 * DOID:0111391
 * mucopolysaccharidosis type IVB
 * class of disease
 * autosomal recessive disease Morquio syndrome
 * human disease
 * DOID:0111392
 * mucormycosis
 * class of disease symptom or sign
 * zygomycosis opportunistic mycosis disease
 * fungal infection by the order Mucorales
 * DOID:8485 DOID:0050595
 * C01.150.703.980.600
 * [[File:Periorbital fungal infection known as mucormycosis, or phycomycosis PHIL 2831 lores.jpg|center|64px]]
 * mucosal melanoma
 * class of disease
 * melanoma extracutaneous melanoma
 * melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract
 * DOID:0050929
 * mucositis
 * class of disease
 * skin disease gastrointestinal system disease
 * gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract
 * DOID:0080178
 * C06.405.205.798 C07.465.584
 * Mucositis
 * multicentric papillary thyroid carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:7086
 * multicentric reticulohistiocytosis
 * class of disease
 * Reticulohistiocytosis syndrome
 * syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis
 * DOID:11824
 * multifocal dystonia
 * class of disease
 * dystonia
 * dystonia that involves two or more unrelated body parts
 * DOID:0050837
 * multifocal osteogenic sarcoma
 * class of disease
 * osteosarcoma bone sarcoma
 * Human disease
 * DOID:3360
 * multilocular cystic clear cell renal cell carcinoma
 * class of disease
 * renal cell carcinoma renal clear cell carcinoma
 * human disease
 * DOID:4463
 * multiminicore disease
 * class of disease
 * human disease
 * DOID:0080991
 * multinodular goiter
 * class of disease
 * goiter nodular goiter
 * goiter characterized by a multinodular enlargement of the thyroid gland
 * DOID:0050489
 * multiple benign circumferential skin creases on limbs
 * class of disease
 * skin disease
 * human disease
 * DOID:0112241
 * multiple chemical sensitivity
 * class of disease
 * syndrome
 * chronic medical condition of disputed but probably multifactorial etiology (genetic and non-genetic)
 * DOID:4661
 * C20.543.312.500 C21.223.500
 * Multiple chemical sensitivity
 * multiple congenital anomalies-hypotonia-seizures syndrome
 * class of disease
 * lipid metabolism disorder
 * lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency
 * DOID:0080503
 * multiple cranial nerve palsy
 * class of disease
 * glossopharyngeal nerve disease cranial nerve disease
 * Human disease
 * DOID:13866
 * multiple endocrine neoplasia
 * class of disease
 * endocrine gland neoplasm multiple polyglandular tumor
 * human disease
 * DOID:3125
 * C04.588.322.400 C04.651.600 C04.700.630 C16.320.700.630 C19.344.400
 * Multiple endocrine neoplasia
 * multiple epiphyseal dysplasia 2
 * class of disease
 * multiple epiphyseal dysplasia genetic disease autosomal dominant disease multiple epiphyseal dysplasia due to collagen 9 anomaly
 * multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A2 gene on chromosome 1p34
 * DOID:0070298
 * multiple epiphyseal dysplasia 3
 * class of disease
 * multiple epiphyseal dysplasia genetic disease multiple epiphyseal dysplasia due to collagen 9 anomaly autosomal dominant disease
 * multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A3 gene on chromosome 20q13
 * DOID:0070304
 * multiple epiphyseal dysplasia 7
 * class of disease
 * multiple epiphyseal dysplasia genetic disease autosomal recessive disease
 * multiple epiphyseal dysplasia that has material basis in homozygous mutation in the CANT1 gene on chromosome 17q25
 * DOID:0070302
 * multiple epiphyseal dysplasia due to collagen 9 anomaly
 * class of disease
 * multiple epiphyseal dysplasia genetic disease monogenic disease
 * multiple epiphyseal dysplasia that has material basis in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3)
 * DOID:0070305
 * multiple epiphyseal dysplasia with myopia and deafness
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0111348
 * multiple mitochondrial dysfunctions syndrome 6
 * class of disease
 * fatal multiple mitochondrial dysfunctions syndrome autosomal recessive disease
 * human disease
 * DOID:0070332
 * multiple mucosal neuroma
 * class of disease
 * neuroma
 * Human disease
 * DOID:5155
 * multiple myeloma
 * class of disease
 * leukocyte disease myeloid neoplasm immunoproliferative disorder disease
 * cancer of plasma cells
 * DOID:9538
 * C04.557.595.500 C14.907.454.460 C15.378.147.780.650 C15.378.463.515.460 C20.683.515.845 C20.683.780.650
 * Multiple myeloma
 * Plasmozytom multiple Osteolysen Unterarm.png
 * multiple spinal canal and spinal cord meningioma
 * class of disease
 * spinal canal and spinal cord meningioma
 * Human disease
 * DOID:7646
 * multisystem proteinopathy
 * class of disease
 * motor neuron disease
 * human disease
 * DOID:070355
 * mumps
 * class of disease symptom or sign
 * parotitis mumps virus infectious disease herpangina salivary gland disease disease
 * Human disease caused by paramyxovirus
 * DOID:10264
 * C01.925.782.580.600.680.500 C07.465.815.470.800.630
 * Mumps
 * Mumps.jpg
 * muscle neoplasm
 * class of disease
 * soft tissue neoplasm muscular disease
 * tumors or cancer located in muscle tissue or specific muscles
 * DOID:461
 * C04.588.839.500 C05.651.494
 * muscle tissue disease
 * class of disease
 * muscular disease
 * disease involving the muscle tissue
 * DOID:66
 * muscular atrophy
 * class of disease
 * muscular disease atrophic muscular disease clinical sign
 * human disease
 * DOID:767
 * C10.597.613.612 C23.300.070.500 C23.888.592.608.612
 * Muscle wasting
 * musculoskeletal disorder
 * class of disease
 * disease of anatomical entity
 * disease of anatomical entity that occurs in the muscular and/or skeletal system
 * DOID:17
 * C05
 * Diseases and disorders of the musculoskeletal system
 * Ankle Joint Arthritis.jpg
 * musculoskeletal system benign neoplasm
 * class of disease
 * organ system benign neoplasm musculoskeletal neoplasm
 * organ system benign neoplasm that is located in the muscular and skeletal organs
 * DOID:0060099
 * musculoskeletal system cancer
 * class of disease
 * organ system cancer musculoskeletal disorder musculoskeletal neoplasm
 * organ system cancer located in the muscular and skeletal organs and characterized by uncontrolled cellular proliferation of the musculoskeletal organs
 * DOID:0060100
 * mushroom workers' lung
 * class of disease
 * extrinsic allergic alveolitis
 * Human disease
 * DOID:2708
 * mycoplasma infection
 * class of disease
 * bacterial infectious disease primary Mycoplasmataceae infectious disease disease
 * bacterial infection with a species of the genus Mycoplasma
 * DOID:0050407 DOID:5461
 * C01.150.252.400.610.610
 * mycosis fungoides
 * class of disease
 * cutaneous T cell lymphoma rare disease mycosis fungoides and variants disease
 * Human disease
 * DOID:8691
 * C04.557.386.480.750.800.550 C15.604.515.569.480.750.800.550 C20.683.515.761.480.750.800.550
 * Mycosis fungoides
 * Mycosis fungoides knee.JPG
 * mycotic corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10440
 * myelitis
 * class of disease
 * spinal cord disease
 * spinal cord disease that is characterized by inflammation of the white matter or gray matter of the spinal cord
 * DOID:322
 * C10.228.228.618 C10.228.854.525
 * Myelitis
 * Living anatomy and pathology; (1910) (14571685858).jpg
 * myelodysplastic syndrome
 * class of disease
 * myeloproliferative disorders neoplastic syndrome disease
 * diverse collection of blood-related medical conditions with ineffective production of the myeloid class of blood cells
 * DOID:0050908
 * C15.378.190.625
 * Myelodysplastic syndrome
 * myelodysplastic/myeloproliferative neoplasm
 * class of disease
 * myeloid neoplasm
 * myeloid neoplasm that results in the overproduction of white blood cells
 * DOID:4972
 * myelofibrosis
 * class of disease
 * myeloid neoplasm acquired aplastic anemia rare genetic immune disease disease
 * myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue
 * DOID:4971
 * C15.378.190.636.765
 * Myelofibrosis, Reticulin Stain (6032644716).jpg
 * myeloid and lymphoid neoplasms associated with FGFR1 abnormalities
 * class of disease
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint
 * DOID:0080167
 * myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
 * class of disease
 * myeloid neoplasm associated with PDGFRA rearrangement myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRA gene, most often resulting in the formation of FIP1L1-PDGFRA fusion transcripts
 * DOID:0080165
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * class of disease
 * myeloid neoplasm myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1
 * human disease
 * DOID:0080164
 * myeloid leukemia
 * class of disease
 * leukemia disease
 * leukemia that is located in myeloid tissue
 * DOID:8692
 * C04.557.337.539
 * Myeloid leukemias
 * myeloid leukemia associated with Down Syndrome
 * class of disease
 * acute megakaryoblastic leukemia
 * human disease
 * DOID:0080798
 * myeloid neoplasm
 * class of disease
 * myeloproliferative disorders
 * a bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages.
 * DOID:0070004
 * myeloid neoplasms associated with PDGFRB rearrangement
 * class of disease
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
 * myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRB gene, most often resulting in the formation of ETV6-PDGFRB fusion transcripts
 * DOID:0080166
 * myeloid sarcoma
 * class of disease
 * hematologic cancer
 * solid tumor composed of immature white blood cells[2] called myeloblasts.
 * DOID:8683
 * C04.557.337.539.775 C04.557.450.795.853
 * Myeloid sarcoma
 * myelophthisic anemia
 * class of disease
 * aplastic anemia
 * aplastic anemia that is characterized by displacement of hemopoietic bone-marrow tissue either by fibrosis, tumors or granulomas
 * DOID:2354
 * C15.378.071.307 C15.378.190.636.085
 * myeloproliferative disorder, chronic, with eosinophilia
 * class of disease
 * myeloproliferative disorders eosinophilia myeloproliferative neoplasm
 * human disease
 * DOID:0111344
 * myeloproliferative disorders
 * class of disease
 * bone marrow disease tumor of hematopoietic and lymphoid tissues connective tissue neoplasm hematologic cancer disease
 * hematopoietic disorders that derive from the blood-forming stem cells of the bone marrow
 * DOID:4960
 * C15.378.190.636
 * Myeloid neoplasms
 * myeloproliferative neoplasm
 * class of disease
 * myeloid neoplasm myeloproliferative disorders
 * myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood
 * DOID:2226
 * myoblastoma
 * class of disease
 * muscle neoplasm
 * human disease
 * DOID:5039
 * myocardial stunning
 * class of disease
 * myocardial infarction
 * state when some section of the myocardium (corresponding to area of a major coronary occlusion) shows a form of contractile abnormality
 * DOID:9767
 * C14.280.671 C23.888.582
 * myocarditis
 * class of disease symptom or sign
 * extrinsic cardiomyopathy myocardial disorder pancarditis cardiovascular system symptom disease
 * extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle
 * DOID:820
 * C14.280.238.625
 * Myocarditis
 * Viral myocarditis (1).JPG
 * myocardium cancer
 * class of disease
 * neoplasm of myocardium heart cancer
 * human disease
 * DOID:9299
 * myoclonic cerebellar dyssynergia
 * class of disease
 * neurodegeneration nervous system heredodegenerative disease Ramsay Hunt syndrome
 * degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment
 * DOID:12707
 * C10.228.140.252.700.250 C10.228.854.787.500 C10.574.500.825.250 C16.320.400.780.500
 * myoclonic dystonia 11
 * class of disease
 * myoclonic dystonia genetic disease autosomal dominant disease
 * myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has material basis in heterozygous mutation in the SGCE gene on chromosome 7q21
 * DOID:0090034
 * myoclonic dystonia 15
 * class of disease
 * myoclonic dystonia genetic disease autosomal dominant disease
 * myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11
 * DOID:0090035
 * myoepithelial carcinoma
 * class of disease
 * carcinoma
 * carcinoma that derives from myoepithelial cells
 * DOID:4838
 * myoepithelioma of the head and neck
 * class of disease
 * sweat gland neoplasm
 * neoplasm composed of outgrowths of myoepithelial cells from a sweat gland
 * DOID:2661
 * C04.557.435.585
 * Myoepithelioma of the head and neck
 * myofascial pain syndrome
 * class of disease
 * muscular disease medically unexplained physical symptom myalgia disease
 * human disease
 * DOID:431
 * C05.651.550
 * myofibrillar myopathy
 * class of disease
 * muscular disease
 * myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles
 * DOID:0080307
 * myofibrillar myopathy 10
 * class of disease
 * autosomal recessive disease myofibrillar myopathy
 * human disease
 * DOID:0112108
 * myofibrillar myopathy 3
 * class of disease
 * myofibrillar myopathy autosomal dominant disease
 * Human disease
 * DOID:0080094
 * myofibroma
 * class of disease
 * connective tissue neoplasm benign perivascular tumor connective tissue benign neoplasm
 * Human disease
 * DOID:4386
 * C04.557.450.565.540 C17.300.680.540
 * Lipoleiomyoma uterus.jpg
 * myoma
 * class of disease
 * muscle neoplasm uterine benign neoplasm disease
 * human disease
 * DOID:2691
 * C04.557.450.590.540
 * Uterine fibroids
 * Uterine fibroids.jpg
 * myopathy of extraocular muscle
 * class of disease
 * peripheral neuropathy rare eye disease muscular disease
 * myopathy that involves the extra-ocular muscle
 * DOID:929
 * myopathy, lactic acidosis, and sideroblastic anemia 1
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * human disease
 * DOID:0111185
 * myopathy, lactic acidosis, and sideroblastic anemia 2
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has material basis in homozyous or compound heterozygous mutation in YARS2 on 12p11.21.
 * DOID:0111186
 * myopathy, lactic acidosis, and sideroblastic anemia 3
 * class of disease
 * myopathy, lactic acidosis, and sideroblastic anemia
 * human disease
 * DOID:0111184
 * myopathy, myofibrillar, 11
 * class of disease
 * myofibrillar myopathy
 * human disease
 * DOID:0081338
 * myopia
 * class of disease symptom or sign
 * refractive error visual impairment disease
 * visual defect which causes to see the near objects clearly and far objects unclearly
 * DOID:11830
 * C11.744.636
 * Myopia
 * Myopia.gif
 * myosarcoma
 * class of disease
 * musculoskeletal system cancer muscle tissue neoplasm muscular disease
 * musculoskeletal system cancer that is located in muscle
 * DOID:4045
 * C04.557.450.590.550 C04.557.450.795.550
 * myositis
 * class of disease
 * muscular disease inflammation disease
 * myopathy characterized by muscle inflammation
 * DOID:633
 * C05.651.594 C10.668.491.562
 * myositis fibrosa
 * class of disease
 * myositis
 * Human disease
 * DOID:9788
 * myositis ossificans
 * class of disease
 * myositis heterotopic ossification
 * myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles
 * DOID:668
 * C05.651.594.638
 * myotonic cataract
 * class of disease
 * cataract
 * Human disease
 * DOID:82
 * myotonic disease
 * class of disease
 * muscular dystrophy
 * muscular dystrophy characterized by progressive muscle wasting and weakness
 * DOID:450
 * C05.651.662 C10.668.491.606
 * myringitis bullosa hemorrhagica
 * class of disease
 * tympanic membrane disease disease
 * tympanic membrane disease that is characterized by blisters on the eardrum resulting from infection
 * DOID:13791
 * myxedema
 * class of disease
 * hypothyroidism mucinosis disease
 * Human disease
 * DOID:11634
 * C17.300.550.590 C19.874.482.638
 * Myxedema
 * myxofibrosarcoma
 * class of disease
 * fibrous histiocytoma skeletal muscle cancer rare nervous system tumor peripheral neuropathy fibrosarcoma fibromyxoid tumor sarcoma
 * A malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.
 * DOID:0080534
 * myxoid chondrosarcoma
 * class of disease
 * chondrosarcoma myxoid tumor
 * human disease
 * DOID:5861
 * myxoid leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5268
 * myxoid liposarcoma of the ovary
 * class of disease
 * liposarcoma of the ovary myxoid liposarcoma
 * Human disease
 * DOID:8023
 * myxomatous pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8081
 * myxopapillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5075
 * myxosarcoma
 * class of disease
 * sarcoma connective tissue neoplasm
 * human disease
 * DOID:4136
 * C04.557.450.565.560 C04.557.450.795.560
 * nail disease
 * class of disease
 * integumentary system disease
 * integumentary system disease that is located in nail
 * DOID:4123
 * C17.800.529
 * Diseases and disorders of the nails
 * nanophthalmos
 * class of disease
 * microphthalmia
 * human disease
 * DOID:0080634
 * narcissistic personality disorder
 * class of disease
 * personality disorder narcissism disease
 * personality disorder that involves an excessive preoccupation with issues of personal adequacy, power, prestige and vanity
 * DOID:2745
 * F03.675.500
 * Narcissistic personality disorder
 * Seesaw narcissism megalomania model.png
 * narcolepsy
 * class of disease
 * disease sleep disorder excessive daytime sleepiness
 * Human sleep disorder that involves an excessive urge to sleep and other neurological features
 * DOID:8986
 * C10.886.425.800.200.750 F03.870.400.800.200.750
 * Narcolepsy
 * nasal cavity cancer
 * class of disease
 * sensory system cancer nasal cancer nasal cavity neoplasm nasal cavity disease respiratory system cancer
 * respiratory system cancer that is located in the nasal cavity
 * DOID:10811
 * nasal cavity disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:2163
 * nasal cavity lymphoma
 * class of disease
 * nasal cavity cancer lymphoma
 * human disease
 * DOID:10813
 * nasal cavity olfactory neuroblastoma
 * class of disease
 * nasal cavity cancer esthesioneuroblastoma
 * Human disease
 * DOID:10812
 * nasopharyngeal disease
 * class of disease
 * upper respiratory tract disease pharyngeal diseases
 * respiratory disease
 * DOID:9561
 * C07.550.350 C09.775.350
 * nasopharyngitis
 * class of disease
 * nasopharyngeal disease
 * respiratory disease
 * DOID:10460
 * C07.550.350.700 C07.550.781.500 C08.730.561.500 C09.775.350.700 C09.775.649.500
 * natural killer cell leukemia
 * class of disease
 * lymphoblastic leukemia leukocyte disease rare bone disease immune disorder disease
 * Human disease
 * DOID:1035
 * near-fatal asthma
 * class of disease
 * acute asthma
 * human disease
 * DOID:0080823
 * necrobiosis lipoidica
 * class of disease
 * skin disease diabetic dermadrome necrobiotic disorders
 * human disease
 * DOID:3486
 * C17.300.200.495.545 C17.800.550.545 C17.800.849.495 C18.452.880.495
 * Necrobiosis lipoidica
 * Necrobiosislipoidica.jpg
 * necrosis of ear ossicle
 * class of disease
 * middle ear disease ear disease
 * Human disease
 * DOID:11783
 * necrosis of pituitary
 * class of disease
 * pituitary gland disease
 * endocrine disease
 * DOID:3646
 * necrotizing enterocolitis
 * class of disease
 * gastrointestinal system disease disease
 * human disease
 * DOID:8677
 * C06.405.205.596.700 C06.405.469.363.700
 * Neonatal necrotizing enterocolitis
 * necrotizing fasciitis
 * class of disease symptom or sign
 * fasciitis necrotizing soft tissue infection disease
 * infection that results in the death of the body&#39;s soft tissue
 * DOID:9602
 * C01.252.825.340 C05.321.550
 * Necrotizing fasciitis
 * Necrotizing fasciitis left leg.JPEG
 * necrotizing gastritis
 * class of disease
 * gastritis necrosis chronic gastritis
 * Human disease
 * DOID:4037
 * necrotizing sialometaplasia
 * class of disease
 * salivary gland disease disease
 * Human disease
 * DOID:12901
 * C07.465.815.802
 * Necrotizing sialometaplasia
 * nemaline myopathy 2
 * class of disease
 * nemaline myopathy genetic disease autosomal recessive disease
 * nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23
 * DOID:0110928
 * nemaline myopathy 3
 * class of disease
 * nemaline myopathy genetic disease autosomal recessive disease
 * nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42
 * DOID:0110927
 * neomycin sulfate allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis drug allergy
 * allergic contact dermatitis that has allergic trigger neomycin sulfate
 * DOID:0040067
 * neonatal anemia
 * class of disease
 * anemia
 * Human disease
 * DOID:11244
 * C15.378.071.363 C16.614.053
 * neonatal diabetes mellitus
 * class of disease
 * diabetes neonatal metabolic disturbances rare genetic diabetes mellitus
 * It is a congenital form of diabetes
 * DOID:11717
 * neonatal infective mastitis
 * class of disease
 * mastitis perinatal infectious disease
 * Human disease
 * DOID:13520
 * neonatal jaundice
 * class of disease
 * pigmentation disorder jaundice neonatal hyperbilirubinemia disease
 * pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant
 * DOID:2383
 * C16.614.451.500 C23.550.429.249.500
 * Neonatal jaundice
 * Jaundice phototherapy.jpg
 * neonatal leukemia
 * class of disease
 * childhood leukemia perinatal disease
 * Human disease
 * DOID:7756
 * neonatal myasthenia gravis
 * class of disease
 * myasthenia gravis
 * Human disease
 * DOID:14043
 * C10.114.656.650 C10.668.758.725.650 C20.111.258.500.650
 * neonatal period electroclinical syndrome
 * class of disease
 * electroclinical syndrome perinatal disease
 * electroclinical syndrome with onset in the neonatal period less than 44 weeks of gestational age
 * DOID:0050702
 * neonatal thyrotoxicosis
 * class of disease
 * thyrotoxicosis
 * endocrine disease
 * DOID:12573
 * neonatal urinary tract infectious disease
 * class of disease
 * urinary system disease urinary tract infection in children perinatal infectious disease
 * Human disease
 * DOID:1375
 * neonatal-onset type II citrullinemia
 * class of disease
 * citrullinemia autosomal recessive disease citrullinemia type II
 * human disease
 * DOID:0070341
 * neovascular glaucoma
 * class of disease
 * glaucoma glaucoma associated with vascular disorder rare acquired eye disease
 * Human disease
 * DOID:1687
 * C11.525.381.348
 * nephritis
 * class of disease symptom or sign
 * urological symptom disease
 * inflammation of the kidneys
 * DOID:10952
 * C12.777.419.570 C13.351.968.419.570
 * Nephritis
 * Diffuse proliferative lupus nephritis.jpg
 * nephrocalcinosis
 * class of disease
 * kidney disease calcinosis
 * Human disease
 * DOID:12679
 * C12.050.351.968.419.590 C12.200.777.419.590 C18.452.174.130.560 C12.950.419.590
 * Nephrocalcinosis
 * nephrogenic adenofibroma
 * class of disease
 * kidney benign neoplasm
 * Human disease
 * DOID:2698
 * nephrogenic adenoma of the urethra
 * class of disease
 * urethral benign neoplasm nephrogenic adenoma adenoma
 * Human disease
 * DOID:8109
 * nephrogenic adenoma of urinary bladder
 * class of disease
 * bladder benign neoplasm nephrogenic adenoma adenoma
 * Human disease
 * DOID:7333
 * nephrogenic diabetes insipidus type 2
 * class of disease
 * autosomal dominant disease nephrogenic diabetes insipidus autosomal recessive disease
 * human disease
 * DOID:0081061
 * nephrolithiasis
 * class of disease
 * kidney disease kidney stone disease
 * Human disease
 * DOID:585
 * C12.200.777.419.600 C12.200.777.967.249 C12.050.351.968.419.600 C12.050.351.968.967.249 C12.950.419.600 C12.950.967.249
 * nephroma
 * class of disease
 * kidney benign neoplasm kidney cortex disease
 * human disease
 * DOID:0080615
 * nephronophthisis
 * class of disease
 * autosomal recessive disease medullary cystic kidney disease kidney disease
 * congenital disorder of urinary system
 * DOID:12712
 * Nephronophthisis
 * nephronophthisis 1
 * class of disease
 * nephronophthisis
 * nephronophthisis that has material basis in homozygous or compound heterozygous mutation in or deletion of the NPHP1 gene on chromosome 2q13
 * DOID:0111112
 * nephropathia epidemica
 * class of disease
 * hemorrhagic fever with renal syndrome
 * human disease
 * DOID:0050201
 * nephrosclerosis
 * class of disease
 * renal hypertension disease
 * medical condition referring to damage to the kidney due to chronic high blood pressure
 * DOID:11664
 * C12.777.419.610 C13.351.968.419.610
 * nephrosis
 * class of disease
 * proteinuria kidney disease
 * non-inflammatory kidney disease
 * DOID:2527
 * C12.777.419.630 C13.351.968.419.630
 * Nephrosis
 * nephrotic syndrome 14
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080265
 * nephrotic syndrome 15
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080271
 * nephrotic syndrome 16
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080272
 * nephrotic syndrome type 1
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13
 * DOID:0080390
 * nephrotic syndrome type 17
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25
 * DOID:0080392
 * nephrotic syndrome type 18
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42
 * DOID:0080393
 * nephrotic syndrome type 19
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome that has material basis in compound heterozygous mutation in the NUP160 gene on chromosome 11p11
 * DOID:0080394
 * nephrotic syndrome type 2
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease nephrotic syndrome
 * human disease
 * DOID:0080379
 * nephrotic syndrome type 20
 * class of disease
 * familial nephrotic syndrome
 * human disease
 * DOID:0070357
 * nephrotic syndrome type 22
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0112268
 * nephrotic syndrome type 3
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has material basis in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23
 * DOID:0080382
 * nephrotic syndrome type 5
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p
 * DOID:0080380
 * nephrotic syndrome type 7
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080388
 * nephrotic syndrome type 8
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25
 * DOID:0080389
 * nephrotic syndrome, type 10
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080386
 * nephrotic syndrome, type 4
 * class of disease
 * nephrotic syndrome familial nephrotic syndrome autosomal dominant disease
 * human disease
 * DOID:0080383
 * nephrotic syndrome, type 6
 * class of disease
 * familial nephrotic syndrome autosomal recessive disease
 * human disease
 * DOID:0080384
 * nephrotic syndrome, type 9
 * class of disease
 * familial nephrotic syndrome
 * human disease
 * DOID:0080391
 * nerve compression syndrome
 * class of disease
 * peripheral neuropathy
 * Human disease
 * DOID:573
 * C10.668.829.550
 * Nerve compression syndromes
 * nerve fibre bundle defect
 * class of disease
 * visual pathway disease retinal disease
 * Human disease
 * DOID:5678
 * nerve plexus neoplasm
 * class of disease
 * peripheral nervous system neoplasm plexopathy
 * Human disease
 * DOID:4693
 * nerve root neoplasm
 * class of disease
 * peripheral nervous system neoplasm radiculopathy
 * Human disease
 * DOID:4698
 * nerve sheath neoplasms
 * class of disease
 * peripheral nervous system neoplasm neoplasm
 * peripheral nervous system neoplasm that is located in the connective tissue surrounding nerves
 * DOID:3193
 * C04.557.580.600 C10.551.775.500 C10.668.829.725.500
 * nervous system benign neoplasm
 * class of disease
 * organ system benign neoplasm neurological disorder nervous system neoplasm
 * organ system benign neoplasm that is located in the central nervous system or located in the peripheral nervous system
 * DOID:0060115
 * nervous system cancer
 * class of disease
 * organ system cancer nervous system neoplasm neurological disorder
 * organ system cancer located in the nervous system that affects the central or peripheral nervous system
 * DOID:3093
 * Nervous system neoplasms
 * nervous system hibernoma
 * class of disease
 * nervous system cancer hibernoma central nervous system lipoma
 * Human disease
 * DOID:6607
 * nervous system malformations
 * class of disease
 * congenital disorder central nervous system disease neurological disorder disease
 * congenital conditions that stem from damage to, or abnormal development of, the budding nervous system
 * DOID:2490
 * C10.500 C16.131.666
 * Congenital diseases and disorders of the nervous system
 * nested variant infiltrating bladder urothelial carcinoma
 * class of disease
 * invasive bladder transitional cell carcinoma
 * human disease
 * DOID:7969
 * neurilemmoma
 * class of disease
 * neuroma disease
 * benign tumor of the nerve sheat composed of Schwann cells
 * DOID:3192
 * C04.557.465.625.650.595 C04.557.580.600.610.595 C04.557.580.625.650.595
 * Schwannoma
 * Peripheral schwannoma Antoni type A (1).JPG
 * neurilemmoma of the fifth cranial nerve
 * class of disease
 * trigeminal nerve neoplasm neurilemmoma
 * Human disease
 * DOID:3202
 * neurilemmoma of the pleura
 * class of disease
 * peripheral nerve schwannoma pleural disease respiratory system benign neoplasm rare respiratory disease benign neoplasm of pleura
 * Human disease
 * DOID:6564
 * neuritis
 * class of disease symptom or sign
 * peripheral neuropathy inflammation disease
 * inflammation of a nerve or the general inflammation of the peripheral nervous system
 * DOID:1803
 * C10.668.829.650
 * Neuritis
 * neuroaxonal dystrophy
 * class of disease
 * cerebral degeneration
 * Human disease
 * DOID:2367
 * C10.228.140.744
 * neurobehavioral disorder with prenatal alcohol exposure
 * class of disease
 * fetal alcohol spectrum disorders
 * human disease
 * DOID:0081052
 * neuroblastoma
 * class of disease cancer
 * autonomic nervous system neoplasm neuroblastic tumor disease childhood cancer
 * autonomic nervous system neoplasm derived from immature nerve cells
 * DOID:769
 * C04.557.465.625.600.590.650.550 C04.557.470.670.590.650.550 C04.557.580.625.600.590.650.550
 * Neuroblastoma
 * Neuroblastoma rosettes.jpg
 * neurocirculatory asthenia
 * class of disease
 * somatoform disorder
 * somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities.
 * DOID:11569
 * F03.080.500
 * neurodegeneration
 * class of disease
 * central nervous system disease degenerative disease disease
 * central nervous system disease
 * DOID:1289
 * C10.574
 * Neurodegenerative diseases and disorders
 * [[File:Parasagittal MRI of human head in patient with benign familial macrocephaly prior to brain injury (ANIMATED).gif|center|64px]]
 * neurodegeneration with brain iron accumulation
 * class of disease
 * iron metabolism disease neurodegeneration genetic neurodegenerative disease with dementia neuroaxonal dystrophy neurometabolic disease metabolic disease with dementia miscellaneous movement disorder due to genetic neurodegenerative disease
 * neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia
 * DOID:0110734
 * neurodegeneration with brain iron accumulation 2A
 * class of disease
 * neurodegeneration with brain iron accumulation genetic disease autosomal recessive disease
 * human disease
 * DOID:0110735
 * neurodegeneration with brain iron accumulation 2B
 * class of disease
 * neurodegeneration with brain iron accumulation Infantile neuroaxonal dystrophy genetic disease autosomal recessive disease
 * human disease
 * DOID:0110736
 * neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
 * class of disease
 * nervous system heredodegenerative disease neurodegeneration autosomal recessive disease
 * hereditary disease in humans
 * DOID:0070352
 * neurodermatitis
 * class of disease symptom or sign
 * dermatitis lichen disease
 * Human disease
 * DOID:3309
 * C17.800.174.660 C17.800.815.660
 * Lichen simplex chronicus
 * Lichen simplex chronicus 1.jpg
 * neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
 * class of disease
 * syndrome neurodevelopmental disorder
 * human disease
 * DOID:0070346
 * neurodevelopmental disorder with midbrain and hindbrain malformations
 * class of disease
 * syndromic intellectual disability genetic disease autosomal recessive disease
 * human disease
 * DOID:0080312
 * neuroectodermal tumor
 * class of disease
 * tumor nervous system cancer
 * Human disease
 * DOID:171
 * C04.557.465.625 C04.557.580.625
 * neuroendocrine carcinoma
 * class of disease
 * carcinoma neuroendocrine tumor
 * carcinoma that derives from neuroendocrine cells
 * DOID:1800
 * C04.557.465.625.650.240 C04.557.470.200.025.370 C04.557.580.625.650.240
 * Large cell neuroendocrine carcinoma Case 120 (4387600323).jpg
 * neuroendocrine tumor
 * class of disease
 * endocrine gland cancer rare disease disease
 * endocrine gland cancer that has material basis in neuroendocrine cells
 * DOID:169
 * C04.557.465.625.650 C04.557.580.625.650
 * Neuroendocrine tumors
 * neurofibroma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:962
 * C04.557.580.600.580 C10.551.775.500.750 C10.668.829.725.500.600
 * Neurofibroma
 * Neurofibroma (1).jpg
 * neurofibroma of gallbladder
 * class of disease
 * neurofibroma gallbladder cancer malignant peripheral nerve neoplasm liver cancer endocrine gland cancer
 * Human disease
 * DOID:5150
 * neurofibroma of spinal cord
 * class of disease
 * neurofibroma Spinal cord cancer
 * human disease
 * DOID:13742
 * neurofibroma of the esophagus
 * class of disease
 * gastrointestinal system disease gastrointestinal system cancer esophageal cancer neurofibroma
 * Human disease
 * DOID:961
 * neurofibroma of the heart
 * class of disease
 * malignant peripheral nerve neoplasm neurofibroma
 * Human disease
 * DOID:9300
 * neurofibromatosis type I
 * class of disease
 * neurofibromatoses neuro-cardio-facial-cutaneous syndromes disease
 * type of neurofibromatosis disease
 * DOID:0111253
 * C04.557.580.600.580.590.650 C04.700.645.650 C10.562.600.500 C10.574.500.549.400 C10.668.829.675 C16.320.400.560.400 C16.320.700.645.650
 * Neurofibromatosis type 1
 * Early neurofibromatosis.jpg
 * neurofibromatosis-Noonan syndrome
 * class of disease
 * syndrome autosomal dominant disease Noonan syndrome and Noonan-related syndrome neurofibromatosis type I
 * human disease
 * DOID:0111683
 * neurofibrosarcoma
 * class of disease
 * neurofibroma
 * Human disease
 * DOID:3512
 * C04.557.450.565.590.350.590 C04.557.450.795.350.590 C04.557.580.600.580.795 C10.551.775.500.750.750 C10.668.829.725.500.600.600
 * neurogenic arthropathy
 * class of disease
 * arthropathy disease
 * Human disease
 * DOID:14286
 * C05.550.186
 * Neuropathic arthropathy
 * neurogenic bladder
 * class of disease
 * bladder disease urination disorder disease
 * Human disease
 * DOID:12143
 * C10.597.900 C12.200.777.829.839 C12.050.351.968.829.760 C23.888.592.900 C12.950.829.760C
 * Neurogenic bladder dysfunction
 * neurogenic bowel
 * class of disease
 * intestinal disease
 * Human disease
 * DOID:13419
 * C06.405.469.158.272.804
 * neurological disorder
 * class of disease
 * disease of anatomical entity disease
 * disease of an anatomical entity located in the central or peripheral nervous system
 * DOID:0060052 DOID:863
 * C10
 * Diseases and disorders of the nervous system
 * Pyramidal hippocampal neuron 40x.jpg
 * neuroma
 * class of disease
 * nervous system benign neoplasm peripheral nervous system neoplasm tumor
 * nervous system benign neoplasm that is characterized as a nerve tissue tumor
 * DOID:2001
 * C04.557.580.600.610
 * Neuroma
 * neuromuscular disease
 * class of disease
 * peripheral neuropathy musculoskeletal disorder disease
 * neuropathy that affect the nerves that control the voluntary muscles
 * DOID:440
 * C10.668
 * Neuromuscular diseases
 * neuromuscular junction disease
 * class of disease
 * neuromuscular disease
 * neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction
 * DOID:439
 * C10.668.758
 * neuronal ceroid lipofuscinosis
 * class of disease
 * lipid storage disease eye degenerative disease nervous system heredodegenerative disease
 * Human disease
 * DOID:14503
 * C10.574.500.550 C16.320.400.600 C16.320.565.398.641.509 C18.452.584.563.641.509 C18.452.648.398.641.509
 * neuronal ceroid lipofuscinosis 1
 * class of disease
 * neuronal ceroid lipofuscinosis Infantile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease juvenile neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110721
 * neuronal ceroid lipofuscinosis 10
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease adult neuronal ceroid lipofuscinosis congenital neuronal ceroid lipofuscinosis genetic disease
 * neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15
 * DOID:0110725
 * neuronal ceroid lipofuscinosis 2
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * A condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
 * DOID:0110726
 * neuronal ceroid lipofuscinosis 3
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis genetic disease
 * A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
 * DOID:0110731
 * neuronal ceroid lipofuscinosis 4A
 * class of disease
 * neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis genetic disease Kufs disease
 * human disease
 * DOID:0110730
 * neuronal ceroid lipofuscinosis 5
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * human disease
 * DOID:0110728
 * neuronal ceroid lipofuscinosis 6
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease adult neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110729
 * neuronal ceroid lipofuscinosis 7
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease genetic disease
 * human disease
 * DOID:0110722
 * neuronal ceroid lipofuscinosis 8
 * class of disease
 * neuronal ceroid lipofuscinosis Jansky–Bielschowsky disease juvenile neuronal ceroid lipofuscinosis genetic disease
 * human disease
 * DOID:0110723
 * neuronal ceroid lipofuscinosis 9
 * class of disease
 * neuronal ceroid lipofuscinosis juvenile neuronal ceroid lipofuscinosis
 * neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seziures
 * DOID:0110733
 * neuronal intestinal dysplasia
 * class of disease
 * colonic disease intestinal pseudo-obstruction intestinal dysganglionosis
 * Human disease
 * DOID:0080072
 * neuronal intestinal dysplasia type A
 * class of disease
 * neuronal intestinal dysplasia
 * human disease
 * DOID:0080679
 * neuronal intestinal dysplasia type B
 * class of disease
 * neuronal intestinal dysplasia
 * human disease
 * DOID:0080680
 * neuronitis
 * class of disease
 * central nervous system disease neurological disorder inflammatory disease disease
 * central nervous system disease that is characterized by neuron inflammation
 * DOID:8117
 * neuronopathy, distal hereditary motor, type 5B
 * class of disease
 * nervous system heredodegenerative disease distal hereditary motor neuronopathy type 5
 * human disease
 * DOID:0111205
 * neurooculocardiogenitourinary syndrome
 * class of disease
 * syndrome autosomal dominant disease
 * human disease
 * DOID:0111675
 * neuropathy
 * class of disease
 * neurological disorder
 * disease of or damage to the nerves
 * DOID:870
 * Neuropathies
 * neuroretinitis
 * class of disease
 * optic papillitis focal chorioretinitis eye disease
 * Human disease
 * DOID:10176
 * neurosarcoidosis
 * class of disease
 * sarcoidosis central nervous system disease
 * disease with granulomas invoving nervous tissue
 * DOID:13403
 * Neurosarcoidosis
 * neurotrophic keratoconjunctivitis
 * class of disease
 * keratoconjunctivitis
 * Human disease
 * DOID:12125
 * neutropenia
 * class of disease
 * agranulocytosis disease
 * abnormally low concentration of neutrophils in the blood
 * DOID:1227
 * C15.378.553.546.184.564 C15.378.243.750.184.564
 * Neutropenia
 * Neutropenia.JPG
 * nevoid basal cell carcinoma syndrome
 * class of disease symptom or sign
 * autosomal dominant disease syndrome
 * an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma
 * DOID:2512
 * C04.182.089.530.690.150 C04.557.470.200.165.150 C04.557.470.565.165.150 C04.700.175 C05.116.099.105 C05.500.470.690.150 C07.320.450.670.130 C16.131.077.130 C16.320.700.175
 * nickel allergic asthma
 * class of disease
 * allergic asthma nickel sensitivity metal allergy
 * allergic asthma that has allergic trigger nickel atom
 * DOID:0040045
 * night blindness
 * class of disease
 * eye disease retinal disease vision disorder disease
 * condition making it difficult or impossible to see in relatively low light
 * DOID:8499
 * C11.966.671
 * Nyctalopia
 * P360 Onderdendam goed nachtzicht ns nachtblind.jpg
 * nipple carcinoma
 * class of disease
 * breast carcinoma malignant neoplasm of nipple
 * breast carcinoma that is located in the nipple
 * DOID:6629
 * nipple duct carcinoma
 * class of disease
 * nipple carcinoma
 * nipple carcinoma that is located in the nipple duct
 * DOID:7953
 * nipple neoplasm
 * class of disease
 * breast benign neoplasm
 * Human disease
 * DOID:3003
 * nocturnal asthma
 * class of disease
 * chronic asthma
 * human disease
 * DOID:0080826
 * nodal marginal zone B cell lymphoma
 * class of disease
 * marginal zone B-cell lymphoma
 * marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease
 * DOID:0080211
 * nodular basal cell carcinoma
 * class of disease
 * basal-cell carcinoma
 * Human disease
 * DOID:4280
 * nodular degeneration of cornea
 * class of disease
 * corneal degeneration
 * Human disease
 * DOID:2879
 * nodular episcleritis
 * class of disease
 * scleral disease episcleritis
 * Human disease
 * DOID:728
 * nodular ganglioneuroblastoma
 * class of disease
 * ganglioneuroblastoma
 * Human disease
 * DOID:5193
 * nodular goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13197
 * C19.874.283.501
 * nodular hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:2061
 * nodular medulloblastoma
 * class of disease
 * medulloblastoma
 * Human disease
 * DOID:3873
 * nodular melanoma
 * class of disease
 * skin melanoma
 * melanoma that is characterized as highly aggressive and manifests as a uniform blue-black, blue-red, or amelanotic nodule
 * DOID:10047
 * Nodular melanoma
 * nodular nonsuppurative panniculitis
 * class of disease
 * panniculitis subcutaneous tissue disease
 * cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin
 * DOID:1525
 * C17.300.710.500 C17.800.566.500
 * nodular prostate
 * class of disease
 * prostatic hypertrophy
 * Human disease
 * DOID:13206
 * nodular tenosynovitis
 * class of disease
 * connective tissue benign neoplasm
 * Human disease
 * DOID:2701
 * non specific chronic endometritis
 * class of disease
 * endometritis chronic endometritis
 * Human disease
 * DOID:4560
 * non-Hodgkin lymphoma
 * class of disease
 * lymphoma neoplasm hematopoietic system disease disease
 * type of cancer of lymph nodes
 * DOID:0060060
 * C04.557.386.480 C15.604.515.569.480 C20.683.515.761.480
 * Non-Hodgkin lymphomas
 * Mantle cell lymphoma - intermed mag.jpg
 * non-Langerhans-cell histiocytosis
 * class of disease
 * histiocytosis
 * Human disease
 * DOID:4330
 * C15.604.250.410
 * non-alcoholic fatty liver
 * class of disease
 * non-alcoholic fatty liver disease
 * nonalcoholic fatty liver disease that is characterized by the presence of at least 5% of hepatic steatosis with no evidence of hepatocellular injury in the form of hepatocyte ballooning
 * DOID:0080546
 * non-alcoholic fatty liver disease
 * class of disease
 * fatty liver disease disease
 * storing of excess fat in liver cells, not caused by heavy alcohol use
 * DOID:0080208
 * C06.552.241.519
 * non-alcoholic steatohepatitis
 * class of disease
 * non-alcoholic fatty liver disease
 * Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure.
 * DOID:0080547
 * non-arteritic anterior ischemic optic neuropathy
 * class of disease
 * anterior ischemic optic neuropathy
 * Human disease
 * DOID:0050864
 * non-congenital cyst of kidney
 * class of disease
 * cystic kidney disease
 * Human disease
 * DOID:9621
 * non-controlled substance abuse
 * class of disease
 * addiction substance use disorder social issue
 * abuse of chemical substances and/or abuse of any licit substances
 * DOID:9973
 * Substance dependence
 * Toxicoman - Substance abuse.jpg
 * non-functioning pancreatic endocrine tumor
 * class of disease
 * islet cell tumor non-functioning endocrine neoplasm
 * Human disease
 * DOID:7698
 * non-gestational choriocarcinoma
 * class of disease
 * choriocarcinoma
 * Human disease
 * DOID:4320
 * C04.557.465.955.207.438 C04.557.470.200.025.455.750 C04.850.908.208.438 C13.703.720.949.208.438
 * non-gestational ovarian choriocarcinoma
 * class of disease
 * ovarian primitive germ cell tumor choriocarcinoma of ovary
 * Human disease
 * DOID:7665
 * non-invasive bladder urothelial carcinoma
 * class of disease
 * bladder urothelial carcinoma
 * human disease
 * DOID:6571
 * non-proliferative fibrocystic change of the breast
 * class of disease
 * breast fibrocystic disease
 * Human disease
 * DOID:5997
 * non-renal secondary hyperparathyroidism
 * class of disease
 * hyperparathyroidism secondary hyperparathyroidism
 * Human disease
 * DOID:13575
 * non-secretory myeloma
 * class of disease
 * multiple myeloma non-functioning endocrine neoplasm
 * Human disease
 * DOID:9547
 * non-small-cell lung carcinoma
 * class of disease
 * lung carcinoma lung cancer disease
 * any type of epithelial lung cancer other than small-cell lung carcinoma
 * DOID:3908
 * C04.588.894.797.520.109.220.249 C08.381.540.140.500 C08.785.520.100.220.500
 * Non-small cell lung cancer
 * non-suppurative otitis media
 * class of disease
 * otitis media
 * otitis media which involves transudation of fluid in the middle ear without pus formation
 * DOID:11180
 * non-syndromic X-linked intellectual disability 1
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112038
 * non-syndromic X-linked intellectual disability 100
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112040
 * non-syndromic X-linked intellectual disability 101
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112048
 * non-syndromic X-linked intellectual disability 103
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112020
 * non-syndromic X-linked intellectual disability 104
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112018
 * non-syndromic X-linked intellectual disability 105
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112036
 * non-syndromic X-linked intellectual disability 107
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112054
 * non-syndromic X-linked intellectual disability 14
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112027
 * non-syndromic X-linked intellectual disability 19
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112019
 * non-syndromic X-linked intellectual disability 2
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112016
 * non-syndromic X-linked intellectual disability 20
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112023
 * non-syndromic X-linked intellectual disability 21
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112022
 * non-syndromic X-linked intellectual disability 23
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112049
 * non-syndromic X-linked intellectual disability 30
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112051
 * non-syndromic X-linked intellectual disability 41
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112058
 * non-syndromic X-linked intellectual disability 42
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112057
 * non-syndromic X-linked intellectual disability 45
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112028
 * non-syndromic X-linked intellectual disability 46
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112055
 * non-syndromic X-linked intellectual disability 50
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112029
 * non-syndromic X-linked intellectual disability 53
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112047
 * non-syndromic X-linked intellectual disability 58
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112024
 * non-syndromic X-linked intellectual disability 63
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112050
 * non-syndromic X-linked intellectual disability 72
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112059
 * non-syndromic X-linked intellectual disability 73
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112017
 * non-syndromic X-linked intellectual disability 77
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112039
 * non-syndromic X-linked intellectual disability 81
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112033
 * non-syndromic X-linked intellectual disability 82
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112052
 * non-syndromic X-linked intellectual disability 84
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112030
 * non-syndromic X-linked intellectual disability 88
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112053
 * non-syndromic X-linked intellectual disability 89
 * class of disease
 * X-linked dominant disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112031
 * non-syndromic X-linked intellectual disability 9
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked recessive disease
 * human disease
 * DOID:0112034
 * non-syndromic X-linked intellectual disability 90
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112041
 * non-syndromic X-linked intellectual disability 91
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112043
 * non-syndromic X-linked intellectual disability 92
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112032
 * non-syndromic X-linked intellectual disability 93
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112045
 * non-syndromic X-linked intellectual disability 96
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112035
 * non-syndromic X-linked intellectual disability 97
 * class of disease
 * non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112046
 * non-syndromic X-linked intellectual disability 98
 * class of disease
 * non-syndromic X-linked intellectual disability X-linked dominant disease
 * human disease
 * DOID:0112044
 * non-syndromic X-linked intellectual disability 99
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112026
 * non-syndromic X-linked intellectual disability ARX-related
 * class of disease
 * X-linked recessive disease non-syndromic X-linked intellectual disability
 * human disease
 * DOID:0112021
 * nonencapsulated sclerosing carcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:5914
 * noninfectious dermatoses of eyelid
 * class of disease
 * blepharitis
 * Human disease
 * DOID:1894
 * noninvasive malignant thymoma
 * class of disease
 * thymoma
 * Human disease
 * DOID:7214
 * nonossifying fibromyxoid tumor
 * class of disease
 * mesenchymal cell neoplasm fibromyxoid tumor
 * Human disease
 * DOID:8305
 * nonphotosensitive trichothiodystrophy
 * class of disease
 * trichothiodystrophy
 * human disease
 * DOID:0111867
 * nonsyndromic aplasia cutis congenita
 * class of disease
 * skin disease aplasia cutis congenita
 * human disease
 * DOID:0080661
 * nonsyndromic congenital nail disorder
 * class of disease
 * nail disease
 * human disease
 * DOID:0080683
 * nonsyndromic congenital nail disorder 1
 * class of disease
 * nail disease Twenty-nail dystrophy inherited isolated nail anomaly epidermal disease nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080079
 * nonsyndromic congenital nail disorder 2
 * class of disease
 * nail disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080080
 * nonsyndromic congenital nail disorder 5
 * class of disease
 * nail disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080083
 * nonsyndromic congenital nail disorder 6
 * class of disease
 * nail disease autosomal dominant disease nonsyndromic congenital nail disorder
 * Human disease
 * DOID:0080084
 * nonsyndromic congenital nail disorder 7
 * class of disease
 * nail disease epidermal disease inherited isolated nail anomaly nonsyndromic congenital nail disorder autosomal dominant disease
 * Human disease
 * DOID:0080085
 * nonsyndromic congenital nail disorder 9
 * class of disease
 * nail disease inherited isolated nail anomaly autosomal recessive disease nonsyndromic congenital nail disorder
 * Human disease
 * DOID:0080087
 * nontoxic goiter
 * class of disease
 * goiter
 * Human disease
 * DOID:13195
 * normal pressure hydrocephalus
 * class of disease
 * communicating hydrocephalus nervous system heredodegenerative disease genetic dementia disease
 * condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure
 * DOID:1572
 * C10.228.140.602.750
 * Normal pressure hydrocephalus
 * normocytic anemia
 * class of disease
 * anemia
 * Human disease
 * DOID:720
 * norwegian scabies
 * class of disease
 * scabies
 * Human disease
 * DOID:14374
 * Crusted scabies
 * Norwegian Scabies in Homeless AIDS Patient.jpg
 * nose disease
 * class of disease
 * upper respiratory tract disease disease
 * respiratory disease
 * DOID:2825
 * C08.460 C09.603
 * Diseases and disorders of the nose and paranasal sinuses
 * notochordal cancer
 * class of disease
 * bone cancer
 * embryonal cancer and bone cancer and mesenchymal cell neoplasm that is located in the notochord
 * DOID:3303
 * nuclear senile cataract
 * class of disease
 * senile cataract nuclear sclerosis
 * Human disease
 * DOID:13963
 * nuclear type mitochondrial complex I deficiency
 * class of disease
 * mitochondrial complex I deficiency
 * human disease
 * DOID:0112065
 * nuclear type mitochondrial complex I deficiency 1
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112074
 * nuclear type mitochondrial complex I deficiency 10
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112075
 * nuclear type mitochondrial complex I deficiency 11
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112089
 * nuclear type mitochondrial complex I deficiency 12
 * class of disease
 * nuclear type mitochondrial complex I deficiency X-linked recessive disease
 * human disease
 * DOID:0112099
 * nuclear type mitochondrial complex I deficiency 13
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112076
 * nuclear type mitochondrial complex I deficiency 14
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112094
 * nuclear type mitochondrial complex I deficiency 15
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112077
 * nuclear type mitochondrial complex I deficiency 16
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112096
 * nuclear type mitochondrial complex I deficiency 17
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112078
 * nuclear type mitochondrial complex I deficiency 18
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112070
 * nuclear type mitochondrial complex I deficiency 19
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112085
 * nuclear type mitochondrial complex I deficiency 2
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112083
 * nuclear type mitochondrial complex I deficiency 20
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112072
 * nuclear type mitochondrial complex I deficiency 21
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112088
 * nuclear type mitochondrial complex I deficiency 22
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112069
 * nuclear type mitochondrial complex I deficiency 23
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112087
 * nuclear type mitochondrial complex I deficiency 24
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112079
 * nuclear type mitochondrial complex I deficiency 25
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112067
 * nuclear type mitochondrial complex I deficiency 26
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112086
 * nuclear type mitochondrial complex I deficiency 27
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112090
 * nuclear type mitochondrial complex I deficiency 28
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112095
 * nuclear type mitochondrial complex I deficiency 29
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112084
 * nuclear type mitochondrial complex I deficiency 3
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112093
 * nuclear type mitochondrial complex I deficiency 30
 * class of disease
 * nuclear type mitochondrial complex I deficiency X-linked recessive disease
 * human disease
 * DOID:0112098
 * nuclear type mitochondrial complex I deficiency 31
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112071
 * nuclear type mitochondrial complex I deficiency 32
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112080
 * nuclear type mitochondrial complex I deficiency 33
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112097
 * nuclear type mitochondrial complex I deficiency 34
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112091
 * nuclear type mitochondrial complex I deficiency 35
 * class of disease
 * autosomal recessive disease mitochondrial complex I deficiency nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112139
 * nuclear type mitochondrial complex I deficiency 4
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112082
 * nuclear type mitochondrial complex I deficiency 5
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112068
 * nuclear type mitochondrial complex I deficiency 6
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112066
 * nuclear type mitochondrial complex I deficiency 7
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112092
 * nuclear type mitochondrial complex I deficiency 8
 * class of disease
 * nuclear type mitochondrial complex I deficiency autosomal recessive disease
 * human disease
 * DOID:0112081
 * nuclear type mitochondrial complex I deficiency 9
 * class of disease
 * autosomal recessive disease nuclear type mitochondrial complex I deficiency
 * human disease
 * DOID:0112073
 * null-cell leukemia
 * class of disease
 * acute lymphocytic leukemia
 * Human disease
 * DOID:9954
 * nutmeg liver
 * class of disease
 * hepatic vascular disease
 * human disease
 * DOID:13739
 * Congestive hepatopathy
 * nutrition disorder
 * class of disease
 * acquired metabolic disease nutritional and metabolic diseases food-related disease
 * disease that results from excessive or inadequate intake of food and nutrients
 * DOID:374
 * C18.654
 * Nutritional diseases and disorders
 * nutritional deficiency disease
 * class of disease
 * nutrition disorder deficiency
 * human disease
 * DOID:5113
 * C18.654.521.500
 * Diseases and disorders due to nutritional deficiencies
 * nutritional optic neuropathy
 * class of disease
 * optic nerve disease optic neuritis
 * Human disease
 * DOID:1209
 * nystagmus, congenital, autosomal recessive
 * class of disease
 * congenital nystagmus autosomal recessive disease
 * human disease
 * DOID:0111797
 * obsessive-compulsive disorder
 * class of disease
 * anxiety disorder impulse control disorder genetic nervous system disorder genetic disease disease
 * anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)
 * DOID:10933
 * F03.080.600
 * Obsessive–compulsive disorder
 * Obsessive-compulsive disorder world map - DALY - WHO2002.svg
 * obsessive-compulsive personality disorder
 * class of disease
 * personality disorder disease
 * personal perfectionism at the cost of flexibility, openness, efficiency & effect on others
 * DOID:10932
 * F03.675.150
 * Obsessive compulsive personality disorder
 * obstructive hydrocephalus
 * class of disease
 * hydrocephalus
 * abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of an obstruction at any location within the ventricular system that prevents cerebrospinal fluid flowing into the subarachnoid space
 * DOID:14159
 * obstructive jaundice
 * class of disease
 * cholestasis jaundice non-neoplastic bile duct disorder
 * Human disease
 * DOID:13603
 * C23.550.429.500.755 C23.888.885.375.500
 * Obstructive jaundice
 * obstructive lung disease
 * class of disease
 * lung disease disease
 * category of respiratory disease characterized by airway obstruction
 * DOID:2320
 * C08.381.495
 * obstructive nephropathy
 * class of disease
 * kidney disease
 * kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction
 * DOID:0070314
 * obstructive sleep apnea
 * class of disease
 * sleep apnea
 * obstruction of the upper airway during sleep
 * DOID:0050848
 * C08.618.085.852.850 C10.886.425.800.750.850
 * occipital lobe neoplasm
 * class of disease
 * cerebrum cancer
 * Human disease
 * DOID:910
 * occlusion of gallbladder
 * class of disease
 * gallbladder disease
 * Human disease
 * DOID:9714
 * occlusion precerebral artery
 * class of disease
 * cerebrovascular disease
 * human disease
 * DOID:5976
 * occupational asthma
 * class of disease
 * occupational disease asthma environmental induced asthma
 * medical condition caused or exacerbated by the workplace
 * DOID:0080820
 * C08.127.108.495 C08.674.095.495 C20.543.480.680.095.495 C24.102
 * occupational dermatitis
 * class of disease
 * contact dermatitis occupational disease disease
 * Human disease
 * DOID:4404
 * C17.800.174.255.700 C17.800.815.255.700 C24.270
 * ochronosis
 * class of disease
 * connective tissue disease clinical sign disease
 * syndrome caused by the accumulation of homogentisic acid in connective tissues
 * DOID:14223
 * C23.550.744
 * Ochronosis
 * Homogentisic acid.svg
 * ocular albinism
 * class of disease
 * eye disease albinism disease
 * human disease
 * DOID:0050633
 * C11.270.040.090 C16.320.290.040.090 C16.320.565.100.102.090 C16.320.850.080.090 C17.800.621.440.102.090 C17.800.827.080.090 C18.452.648.100.102.090
 * ocular albinism type 2
 * class of disease
 * ocular albinism eye disease X-linked recessive disease
 * Human disease
 * DOID:0050630
 * ocular albinism with sensorineural deafness
 * class of disease
 * ocular albinism Waardenburg's syndrome autosomal dominant disease digenic disease
 * human disease
 * DOID:0090100
 * ocular cancer
 * class of disease
 * sensory system cancer eye tumor eye disease disease
 * type of cancer un the eye
 * DOID:2174
 * ocular hyperemia
 * class of disease
 * conjunctival disease
 * Human disease
 * DOID:1248
 * ocular hypertension
 * class of disease
 * eye disease hypertension disease
 * eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss
 * DOID:9282
 * C11.525
 * ocular hypotension
 * class of disease
 * eye disease hypotension
 * Human disease
 * DOID:790
 * C11.540
 * ocular motility disease
 * class of disease
 * cranial nerve disease eye adnexa disease eye disease
 * human disease
 * DOID:1279
 * C10.228.758 C10.292.562 C11.590
 * ocular tuberculosis
 * class of disease
 * extrapulmonary tuberculosis eye disease tuberculosis
 * Human disease
 * DOID:233 DOID:0070344
 * C01.150.252.289.800 C01.375.354.800 C11.294.354.800
 * oculocutaneous albinism type 2
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13
 * DOID:0070096
 * oculocutaneous albinism type 3
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of TYRP1 on chromosome 9p23
 * DOID:0070097
 * oculocutaneous albinism type 4
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.
 * DOID:0070098
 * oculocutaneous albinism type IA
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.
 * DOID:0070094
 * oculocutaneous albinism type IB
 * class of disease
 * oculocutaneous albinism
 * An oculocutaneous albinism that has material basis in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.
 * DOID:0070095
 * oculocutaneous albinism type V
 * class of disease
 * oculocutaneous albinism
 * oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA5 on chromosome 4q24
 * DOID:0070099
 * oculoglandular tularemia
 * class of disease
 * tularemia
 * tularemia that results in inflammation of eye and swelling of lymph glands in front of the ear
 * DOID:13226
 * oculogyric crisis
 * class of disease
 * focal dystonia disease
 * focal dystonia that is characterized by a prolonged involuntary upward deviation of the eyes
 * DOID:0050842
 * oculomotor nerve paralysis
 * class of disease
 * third cranial nerve disease paralytic squint
 * Human disease
 * DOID:11550
 * C10.292.562.700 C11.590.436
 * Oculomotor nerve palsy
 * oculopharyngodistal myopathy 4
 * class of disease
 * Oculopharyngodistal myopathy
 * human disease
 * DOID:0081300
 * odontoclasia
 * class of disease
 * dental caries
 * Human disease
 * DOID:11736
 * olecranon bursitis
 * class of disease
 * enthesopathy bursitis disease
 * Human disease
 * DOID:12581
 * Olecranon bursitis
 * Bursitis Elbow WC.JPG
 * olfactory groove meningioma
 * class of disease
 * anterior cranial fossa meningioma
 * Human disease
 * DOID:8057
 * olfactory nerve disease
 * class of disease
 * glossopharyngeal nerve disease encephalopathy
 * Human disease
 * DOID:367
 * C10.292.650
 * oligoasthenoteratospermia
 * class of disease
 * oligospermia Teratospermia asthenozoospermia male infertility
 * A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.
 * DOID:0070311
 * oligodendroglioma
 * class of disease
 * glioma disease
 * type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell
 * DOID:3181
 * C04.557.465.625.600.380.590 C04.557.470.670.380.590 C04.557.580.625.600.380.590
 * Oligodendrogliomas
 * Oligodendroglioma1 high mag.jpg
 * oligohydramnios
 * class of disease
 * placenta disease disease
 * placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion
 * DOID:12215
 * C13.703.560
 * Oligohydramnios
 * oligospermia
 * class of disease
 * male infertility disease
 * semen with abnormally low concentration of sperm
 * DOID:14228
 * C12.294.365.700.508
 * Oligospermia
 * olivopontocerebellar atrophy
 * class of disease
 * neurodegeneration
 * group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives
 * DOID:14784
 * C10.177.575.550.375 C10.228.140.079.612.600 C10.228.140.252.700.650 C10.228.662.550.600 C10.228.854.787.750 C10.574.500.825.650 C10.574.625.600 C16.320.400.780.750
 * omphalocele
 * class of disease
 * congenital disorder abdominal wall defect disease
 * physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac
 * DOID:0060327
 * Omphalocele
 * oncocytic breast carcinoma
 * class of disease
 * breast adenocarcinoma invasive breast carcinoma
 * Human disease
 * DOID:6585
 * oophoritis
 * class of disease symptom or sign
 * ovarian disease inflammatory disease disease
 * human disease
 * DOID:10974
 * C13.351.500.056.630.450 C13.351.500.056.750.500 C19.391.630.450
 * open-angle glaucoma
 * class of disease
 * glaucoma
 * glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage
 * DOID:1067
 * C11.525.381.407
 * ophthalmia neonatorum
 * class of disease
 * gonococcal eye infectious disease bacterial conjunctivitis
 * Human disease
 * DOID:9699
 * ophthalmia nodosa
 * class of disease
 * eye disease
 * Human disease
 * DOID:9722
 * ophthalmomyiasis
 * class of disease
 * myiasis eye disease parasitic eye infection
 * myiasis that involves parasitic infestation of Oestrus ovis larvae in the eye causing severe irritation, edema, and pain
 * DOID:0050268
 * ophthalmoplegia
 * class of disease symptom or sign
 * ocular motility disease paralysis disease
 * Human disease
 * DOID:539
 * C10.292.562.750 C10.597.622.447 C11.590.472 C23.888.592.636.447
 * Ophthalmoparesis
 * opiate dependence
 * class of disease
 * substance dependence opioid use disorder
 * drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance
 * DOID:2559
 * opioid use disorder
 * class of disease
 * addiction substance abuse opioid-related disorders disease
 * substance abuse disorder that involves the recurring use of opioid drugs despite negative consequences
 * DOID:11206
 * Opioid use disorder
 * opportunistic bacterial infectious disease
 * class of disease
 * bacterial infectious disease opportunistic infection
 * bacterial infectious disease that results in infection by bacteria in individuals whose host defense mechanisms have been compromised
 * DOID:0050340
 * opportunistic mycosis
 * class of disease
 * systemic mycosis opportunistic infection
 * A systemic mycosis that results in fungal infection located in human body of immunocompromised individuals, has material basis in Fungi. The organisms invade via the respiratory tract, alimentary tract, or intravascular devices.
 * DOID:2473
 * oppositional defiant disorder
 * class of disease
 * specific developmental disorder emotional and behavioral disorders disease
 * human disorder involving hostility and defiance
 * DOID:0050856
 * F03.625.094.475
 * Oppositional defiant disorder
 * optic atrophy 10
 * class of disease
 * autosomal dominant disease optic atrophy
 * human disease
 * DOID:0111434
 * optic atrophy 11
 * class of disease
 * autosomal recessive isolated optic atrophy autosomal recessive disease optic atrophy
 * human disease
 * DOID:0111436
 * optic atrophy 2
 * class of disease
 * optic atrophy
 * human disease
 * DOID:0111443
 * optic atrophy 4
 * class of disease
 * Kjer's optic neuropathy optic atrophy autosomal dominant disease
 * human disease
 * DOID:0111440
 * optic atrophy 5
 * class of disease
 * Kjer's optic neuropathy optic atrophy autosomal dominant disease
 * human disease
 * DOID:0111438
 * optic atrophy 6
 * class of disease
 * autosomal recessive isolated optic atrophy optic atrophy autosomal recessive disease
 * human disease
 * DOID:0111435
 * optic atrophy 9
 * class of disease
 * autosomal recessive disease optic atrophy
 * human disease
 * DOID:0111442
 * optic disk drusen
 * class of disease
 * optic nerve disease
 * Human disease
 * DOID:13561
 * C10.292.700.450 C11.640.513
 * optic nerve astrocytoma
 * class of disease
 * optic nerve glioma optic nerve disease astrocytoma neuromuscular disease
 * human disease
 * DOID:4991
 * optic nerve disease
 * class of disease
 * cranial nerve disease vision disorder peripheral neuropathy visual pathway disease neuro-ophthalmological disease disease
 * cranial nerve disease that is located in the optic nerve
 * DOID:1891
 * C10.292.700 C11.640
 * Optic neuropathy
 * optic nerve glioma
 * class of disease
 * optic nerve tumor glioma visual pathway glioma brain glioma
 * human disease
 * DOID:4992
 * C04.557.465.625.600.380.795 C04.557.470.670.380.795 C04.557.580.625.600.380.795 C04.588.614.300.600.600 C04.588.614.596.240.240.500 C10.292.225.800.500 C10.292.700.500.500 C10.551.360.500.500 C10.551.775.250.500.500 C11.640.544.500
 * optic neuritis
 * class of disease
 * optic nerve disease eye disease encephalomyelitis disease
 * optic nerve disease that results in inflammation located in optic nerve which may cause a complete or partial loss of vision
 * DOID:1210
 * C10.292.700.550 C11.640.576
 * Optic neuritis
 * optic papillitis
 * class of disease
 * optic neuritis
 * human disease
 * DOID:10175
 * oral cavity carcinoma in situ
 * class of disease
 * in situ carcinoma mouth cancer mouth disease carcinoma in situ of digestive organ
 * Human disease
 * DOID:0050610
 * oral hairy leukoplakia
 * class of disease
 * mouth disease oral mucosa leukoplakia disease
 * mouth disease characterized by a white patch on the lateral sides of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus
 * DOID:0060315
 * C01.925.256.466.313.500 C04.588.443.591.545.500 C04.834.512.513.500 C07.465.565.545.500 C23.300.816.513.500
 * oral leukoedema
 * class of disease
 * mouth disease Leukoedema
 * Human disease
 * DOID:4557
 * C07.465.385
 * oral mucosa leukoplakia
 * class of disease
 * mouth disease leukoplakia
 * Human disease
 * DOID:9655
 * C04.588.443.591.545 C04.834.512.513 C07.465.565.545 C23.300.816.513
 * Oral leukoplakia
 * oral submucous fibrosis
 * class of disease
 * mouth disease rare maxillo-facial surgical disease
 * human disease
 * DOID:5773
 * C07.465.654
 * oral-facial-digital syndrome
 * class of disease
 * syndrome
 * genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene
 * DOID:4501
 * C05.116.099.370.652 C05.660.207.700 C16.131.077.676 C16.131.260.830.670 C16.131.621.207.700 C16.320.180.830.670 C16.320.714
 * orange allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Citrus sinensis plant fruit food product.
 * DOID:0060508
 * orbit embryonal rhabdomyosarcoma
 * class of disease
 * orbit rhabdomyosarcoma embryonal rhabdomyosarcoma
 * Human disease
 * DOID:3258
 * orbit rhabdomyosarcoma
 * class of disease
 * orbit sarcoma
 * Human disease
 * DOID:3259
 * orbital cancer
 * class of disease
 * bone cancer orbit neoplasm orbital disease
 * Human disease
 * DOID:4143
 * orbital cyst
 * class of disease
 * orbital disease
 * Human disease
 * DOID:14233
 * orbital disease
 * class of disease
 * eye adnexa disease bone disease
 * adnexa disease that is located in the eye socket
 * DOID:930
 * C11.675
 * orbital granuloma
 * class of disease
 * chronic orbital inflammation
 * Human disease
 * DOID:10499
 * orbital osteomyelitis
 * class of disease
 * acute orbital inflammation osteomyelitis
 * Human disease
 * DOID:11232
 * orbital periostitis
 * class of disease
 * acute orbital inflammation
 * human disease
 * DOID:11231
 * orbital tenonitis
 * class of disease
 * acute orbital inflammation
 * Human disease
 * DOID:11233
 * orchitis
 * class of disease
 * testicular disease inflammatory disease disease
 * inflammation of the testes
 * DOID:2518
 * C12.294.829.493 C19.391.829.493
 * Orchitis
 * Orkite cok2 pere polets 32 samwinnes.JPG
 * organ system benign neoplasm
 * class of disease
 * benign neoplasm disease of anatomical entity
 * benign neoplasm that is classified by the organ system from which it is arising from
 * DOID:0060085
 * organ system cancer
 * class of disease
 * cancer cancer by anatomical entity
 * cancer that is classified based on the organ it starts in
 * DOID:0050686
 * C04.588
 * organic acidemia
 * class of disease
 * amino acid metabolic disorder
 * amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids
 * DOID:0060159
 * orofacial cleft 1
 * class of disease
 * cleft lip and cleft palate autosomal dominant disease
 * An orofacial cleft characterized by autosomal dominant inheritance that has material basis in variation in chromosome region 6p24.3.
 * DOID:0080395
 * orofacial cleft 10
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in mutation in the SUMO1 gene on chromosome 2q33
 * DOID:0080403
 * orofacial cleft 11
 * class of disease
 * cleft lip and cleft palate
 * human disease
 * DOID:0080404
 * orofacial cleft 12
 * class of disease
 * cleft lip and cleft palate
 * An orofacial cleft that has material basis in variation in the chromosome region 8q24.3.
 * DOID:0080405
 * orofacial cleft 13
 * class of disease
 * cleft lip and cleft palate autosomal dominant disease
 * orofacial cleft characterized by autosomal doninant inhertitance that has material basis in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730
 * DOID:0080406
 * orofacial cleft 14
 * class of disease
 * cleft lip and cleft palate autosomal recessive disease
 * human disease
 * DOID:0080407
 * orofacial cleft 15
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in mutation in the DLX4 gene on chromosome 17q21
 * DOID:0080408
 * orofacial cleft 2
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the chromosome region 2p13
 * DOID:0080396
 * orofacial cleft 3
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the chromosomal region 19q13
 * DOID:0080397
 * orofacial cleft 4
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in variation in the 4q21-q31 chromosomal region
 * DOID:0080398
 * orofacial cleft 5
 * class of disease
 * cleft lip and cleft palate
 * human disease
 * DOID:0080399
 * orofacial cleft 6
 * class of disease
 * autosomal dominant disease cleft lip and cleft palate
 * human disease
 * DOID:0080593
 * orofacial cleft 7
 * class of disease
 * cleft lip and cleft palate autosomal recessive disease
 * orofacial cleft that has material basis in by homozygous mutation in the PVRL1 gene on chromosome 11q23
 * DOID:0080400
 * orofacial cleft 8
 * class of disease
 * cleft lip and cleft palate
 * orofacial cleft that has material basis in heterozygous mutation in the TP63 gene on chromosome 3q28
 * DOID:0080401
 * orofacial cleft 9
 * class of disease
 * cleft lip and cleft palate
 * An orofacial cleft that has material basis in variation in the chromosome region 13q33.1-q34.
 * DOID:0080402
 * orofaciodigital syndrome VIII
 * class of disease
 * oral-facial-digital syndrome X-linked recessive disease
 * human disease
 * DOID:0060378
 * oromandibular dystonia
 * class of disease
 * focal dystonia lingual-facial-buccal dyskinesia focal, segmental or multifocal dystonia
 * focal dystonia that is characterized by distortions of the mouth and tongue.
 * DOID:0050843
 * oropharyngeal anthrax
 * class of disease
 * gastrointestinal anthrax
 * human disease
 * DOID:0050059
 * orthostatic proteinuria
 * class of disease symptom or sign
 * kidney disease proteinuria
 * Human disease
 * DOID:9617
 * osmotic diarrhea
 * class of disease
 * diarrhea chronic diarrhea
 * Human disease
 * DOID:0050130
 * ossifying fibroma
 * class of disease
 * bone benign neoplasm
 * bone benign neoplasm that is located in the mouth and results in an overgrowth of gingival tissue due to irritation or trauma
 * DOID:180
 * C04.557.450.565.575.400 C04.557.450.565.590.340.360
 * ossifying fibromyxoid tumour
 * class of disease
 * fibromyxoid tumor mesenchymal cell neoplasm
 * human disease
 * DOID:2685
 * osteoarticular tuberculosis
 * class of disease
 * extrapulmonary tuberculosis bone disease
 * extrapulmonary tuberculosis that results in formation of lesions located in bone
 * DOID:1639
 * C01.150.252.410.040.552.846.617.525 C01.160.886 C05.116.165.886
 * osteoblastoma
 * class of disease
 * bone benign neoplasm osteogenic neoplasm disease
 * Human disease
 * DOID:0060098
 * C04.557.450.565.575.600
 * Osteoblastoma
 * Osteoblastoma - high mag.jpg
 * osteochondrodysplasia
 * class of disease
 * bone development disease
 * bone development disease that results in defective development of cartilage or bone
 * DOID:2256
 * C05.116.099.708 C16.320.728
 * Osteochondrodysplasias
 * osteochondrosis
 * class of disease symptom or sign
 * ischemic bone disease disease
 * ischemic bone disease that results in necrosis followed by regrowth in children and teens located in bone
 * DOID:8125
 * C05.116.821
 * Osteochondrosis
 * osteoclast-like giant cell neoplasm of the pancreas
 * class of disease
 * pancreatic ductal adenocarcinoma undifferentiated pancreatic carcinoma
 * Human disease
 * DOID:7718
 * osteogenesis imperfecta 21
 * class of disease
 * osteogenesis imperfecta
 * human disease
 * DOID:0112201
 * osteogenesis imperfecta type 1
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by bone fragility and blue sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110334
 * osteogenesis imperfecta type 16
 * class of disease
 * osteogenesis imperfecta
 * osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
 * DOID:0110345
 * osteogenesis imperfecta type 18
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111848
 * osteogenesis imperfecta type 20
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111849
 * osteogenesis imperfecta type 3
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has material basis in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110339
 * osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
 * class of disease
 * osteogenesis imperfecta dentinogenesis imperfecta blue sclera
 * osteogenesis imperfecta found in a single South African family
 * DOID:0110335
 * osteomalacia
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone
 * DOID:10573
 * C05.116.198.816.640 C18.452.104.816.640 C18.452.174.845.640 C18.654.521.500.133.770.734.640
 * Calcitriol.svg
 * osteomyelitis
 * class of disease
 * bone inflammation disease infectious disease disease
 * bone inflammation disease that has material basis in infection located in bone or located in bone marrow
 * DOID:1019
 * C01.160.495 C05.116.165.495
 * Osteomyelitis
 * osteonecrosis
 * class of disease symptom or sign
 * necrosis ischemic bone disease disease
 * bone death caused when the bone no longer receives blood supply
 * DOID:10159
 * C05.116.852 C23.550.717.732
 * Aseptic osteonecrosis
 * Head of femur avascular necrosis.jpg
 * osteopoikilosis
 * class of disease
 * osteosclerosis
 * osteosclerosis that results in numerous bone islands located in skeleton
 * DOID:11991
 * C05.116.099.708.702.685 C17.300.705
 * Osteopoikilosis
 * osteoporosis
 * class of disease
 * bone resorption disease disease
 * bone resorption disease characterized by the thinning of bone tissue and decreased mechanical strength
 * DOID:11476
 * C05.116.198.579 C18.452.104.579
 * Osteoporosis
 * Osteoporosis -- Smart-Servier.jpg
 * osteosarcoma
 * class of disease
 * bone cancer cell type cancer bone sarcoma osteogenic neoplasm disease childhood cancer
 * bone cancer that is located in bone that has material basis in cells of mesenchymal origin
 * DOID:3347
 * C04.557.450.565.575.650 C04.557.450.795.620
 * Osteosarcoma
 * Osteosarcoma.jpg
 * osteosarcoma arising in bone Paget's disease
 * class of disease
 * bone osteosarcoma mammary Paget's disease
 * Human disease
 * DOID:7542
 * osteosclerosis
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that results in abnormal elevated bone density or mass
 * DOID:4254
 * C05.116.099.708.702
 * ScleroticmetastaticdiseasePelvis.png
 * otomycosis
 * class of disease symptom or sign
 * otitis externa dermatomycosis disease
 * human disease
 * DOID:0050147
 * C01.150.703.658 C09.218.736
 * Otomycosis
 * Otomycosis.jpg
 * otopalatodigital syndrome spectrum disorder
 * class of disease
 * bone development disease
 * DOID:0111782
 * otosclerosis
 * class of disease
 * inner ear disease disease
 * otitis interna characterized by an abnormal bone growth in the middle ear
 * DOID:12185
 * C09.218.768
 * Otosclerosis
 * Gray919.png
 * otospondylomegaepiphyseal dysplasia, autosomal dominant
 * class of disease
 * osteochondrodysplasia autosomal dominant disease
 * human disease
 * DOID:0080677
 * outlet dysfunction constipation
 * class of disease
 * constipation
 * Human disease
 * DOID:2088
 * ovarian Brenner tumor
 * class of disease
 * ovarian benign neoplasm
 * ovarian benign neoplasm that has material basis in the surface epithelium of the ovary
 * DOID:2636
 * Brenner tumour
 * ovarian Wilms' cancer
 * class of disease
 * ovarian cancer
 * malignant neoplasm of ovary and nephroblastoma that is located in the ovaries
 * DOID:2153
 * ovarian angiosarcoma
 * class of disease
 * angiosarcoma ovary sarcoma sarcoma ovarian cancer
 * human disease
 * DOID:4527
 * ovarian benign neoplasm
 * class of disease
 * female reproductive organ benign neoplasm ovarian neoplasm endocrine organ benign neoplasm ovarian disease
 * human disease
 * DOID:0060112
 * Benign neoplasms of the ovary
 * ovarian biphasic or triphasic teratoma
 * class of disease
 * ovarian germ cell teratoma
 * Human disease
 * DOID:6232
 * ovarian cancer
 * class of disease
 * female reproductive organ cancer ovarian neoplasm ovarian disease endocrine gland cancer rare genetic endocrine disease inherited gynecological tumor disease
 * female reproductive organ cancer that is located in the ovary
 * DOID:2394
 * Ovarian cancer
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian carcinoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinoma
 * human disease
 * DOID:4001
 * ovarian carcinosarcoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinosarcoma mixed Müllerian tumor
 * Human disease
 * DOID:6170
 * ovarian clear cell adenocarcinoma
 * class of disease
 * ovary adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5304
 * ovarian clear cell adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5897
 * ovarian clear cell cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma ovarian clear cell adenocarcinoma
 * Human disease
 * DOID:7438
 * ovarian clear cell cystadenofibroma
 * class of disease
 * ovarian clear cell adenofibroma clear cell cystadenofibroma
 * Human disease
 * DOID:5896
 * ovarian clear cell malignant adenofibroma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:6554
 * ovarian cyst
 * class of disease
 * ovarian disease ovarian neoplasm disease
 * fluid-filled sac in the ovary
 * DOID:5119
 * C04.182.612 C13.351.500.056.630.580 C19.391.630.580
 * Ovarian cysts
 * Benign Ovarian Cyst.jpg
 * ovarian cystadenocarcinoma
 * class of disease
 * ovary adenocarcinoma cystadenocarcinoma ovarian cystadenoma
 * human disease
 * DOID:3605
 * ovarian cystadenoma
 * class of disease
 * ovarian benign neoplasm benign epithelial neoplasm
 * human disease
 * DOID:3269
 * ovarian cystic teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:5118
 * Mature cystic teratoma of ovary
 * ovarian disease
 * class of disease
 * female reproductive system disease gonadal disease adnexal disease
 * Human disease
 * DOID:1100
 * C13.351.500.056.630 C19.391.630
 * Diseases and disorders of ovaries
 * ovarian dysfunction
 * class of disease
 * ovarian disease
 * Human disease
 * DOID:1414
 * ovarian dysgenesis 1
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16
 * DOID:0080493
 * ovarian dysgenesis 4
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MCM9 gene on chromosome 6q22
 * DOID:0080496
 * ovarian dysgenesis 5
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the SOHLH1 gene on chromosome 9q34
 * DOID:0080497
 * ovarian dysgenesis 6
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the NUP107 gene on chromosome 12q15
 * DOID:0080498
 * ovarian dysgenesis 7
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MRPS22 gene on chromosome 3q23
 * DOID:0080499
 * ovarian dysgenesis 8
 * class of disease
 * 46 XX gonadal dysgenesis autosomal dominant disease
 * 46 XX gonadal dysgenesis that has material basis in heterozygous mutation in the ESR2 gene on chromosome 14q23
 * DOID:0080500
 * ovarian embryonal carcinoma
 * class of disease
 * embryonal carcinoma malignant non-dysgerminomatous germ cell tumor of ovary ovarian cancer
 * embryonal carcinoma that is located in the ovary
 * DOID:5681
 * ovarian endodermal sinus tumor
 * class of disease
 * ovarian primitive germ cell tumor malignant non-dysgerminomatous germ cell tumor of ovary endodermal sinus tumor
 * Human disease
 * DOID:5350
 * ovarian endometrial cancer
 * class of disease
 * surface epithelial-stromal tumor Endometrioid tumor female reproductive endometrioid cancer
 * ovary epithelial cancer that has material basis in the endometrium and is located in the ovary
 * DOID:6212
 * ovarian endometrioid adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5480
 * ovarian endometrioid cystadenofibroma
 * class of disease
 * ovarian endometrioid adenofibroma cystadenofibroma
 * Human disease
 * DOID:7411
 * ovarian endometrioid cystadenoma
 * class of disease
 * ovarian cystadenoma
 * Human disease
 * DOID:7191
 * ovarian endometrioid malignant adenofibroma
 * class of disease
 * ovarian carcinosarcoma malignant adenofibroma
 * Human disease
 * DOID:6445
 * ovarian endometrioid stromal sarcoma
 * class of disease
 * ovary sarcoma
 * Human disease
 * DOID:5169
 * ovarian fetiform teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6314
 * ovarian germ cell monodermal and highly specialized teratoma
 * class of disease
 * monodermal teratoma
 * Human disease
 * DOID:2641
 * ovarian germ cell neoplasm
 * class of disease
 * ovarian neoplasm germ cell tumor germ cell and embryonal neoplasms ovarian cancer
 * benign or malignant ovarian tumor that originates in the germ (egg) cells of the ovary
 * DOID:2156
 * Germ cell neoplasms
 * ovarian germ cell teratoma
 * class of disease
 * ovarian germ cell neoplasm teratoma gonadal teratoma female reproductive organ cancer
 * Human disease
 * DOID:5567
 * Ovarian teratomas
 * Teratoma Ovary 4x.jpg
 * ovarian gonadoblastoma
 * class of disease
 * ovarian benign neoplasm gonadoblastoma
 * Human disease
 * DOID:3578
 * ovarian large-cell neuroendocrine carcinoma
 * class of disease
 * ovarian carcinoma familiar ovarian carcinoma inherited neuroendocrine tumor large cell neuroendocrine carcinoma
 * Human disease
 * DOID:4555
 * ovarian lymphoma
 * class of disease
 * ovarian cancer lymphoma
 * Human disease
 * DOID:2150
 * ovarian malignant mesothelioma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:2143
 * ovarian melanoma
 * class of disease
 * ovarian cancer
 * ovarian cancer that has material basis in melanoctyes
 * DOID:0050928
 * ovarian mesodermal adenosarcoma
 * class of disease
 * ovarian carcinosarcoma adenosarcoma
 * adenosarcoma and malignant ovarian endometroid tumorthat is located in the ovary
 * DOID:4115
 * ovarian mixed germ cell neoplasm
 * class of disease
 * ovarian primitive germ cell tumor mixed germ cell cancer
 * Human disease
 * DOID:5936
 * ovarian mucinous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma malignant ovarian mucinous tumor mucinous adenocarcinoma
 * human disease
 * DOID:3606
 * ovarian mucinous adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * human disease
 * DOID:6469
 * ovarian mucinous cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma mucinous cystadenocarcinoma ovarian mucinous adenocarcinoma
 * Human disease
 * DOID:3604
 * ovarian mucinous cystadenofibroma
 * class of disease
 * ovarian mucinous adenofibroma mucinous cystadenofibroma
 * Human disease
 * DOID:7013
 * ovarian mucinous malignant adenofibroma
 * class of disease
 * malignant ovarian mucinous tumor malignant adenofibroma ovarian mucinous neoplasm
 * Human disease
 * DOID:6278
 * ovarian mucinous neoplasm
 * class of disease
 * surface epithelial-stromal tumor mucinous tumor
 * Human disease
 * DOID:6067
 * Ovarian mucinous tumors
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian papillary cystadenoma
 * class of disease
 * ovarian papillary neoplasm papillary adenoma ovarian cystadenoma
 * Human disease
 * DOID:6405
 * ovarian papillary neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:6214
 * ovarian primitive germ cell tumor
 * class of disease
 * malignant ovarian germ cell neoplasm
 * Human disease
 * DOID:5351
 * ovarian serous adenofibroma
 * class of disease
 * ovarian benign neoplasm serous adenofibroma
 * Human disease
 * DOID:5474
 * ovarian serous carcinoma
 * class of disease
 * ovarian carcinoma serous carcinoma ovarian serous tumor
 * ovarian carcinoma that has material basis in the lining of the ovary and produces a serum-like fluid
 * DOID:0050933
 * Ovarian serous carcinoma
 * ovarian serous cystadenofibroma
 * class of disease
 * ovarian serous adenofibroma cystadenofibroma
 * Human disease
 * DOID:7320
 * ovarian serous cystadenoma
 * class of disease
 * serous cystadenoma ovarian benign neoplasm ovarian cystadenocarcinoma serous cystadenocarcinoma ovarian cystadenoma ovarian serous tumor
 * ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed
 * DOID:5746 DOID:3914
 * C04.557.470.035.320.240 C04.557.470.590.485.240
 * Ovarian serous cystadenoma
 * Ovarian serous cystadenoma - alt -- low mag.jpg
 * ovarian sex cord-stromal tumor
 * class of disease
 * sex cord-gonadal stromal tumor
 * A benign or malignant neoplasm that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts. Representative examples include thecoma, fibroma, Sertoli cell tumor, and granulosa cell tumor.
 * DOID:0080369
 * ovarian small cell carcinoma
 * class of disease
 * ovarian carcinoma small cell carcinoma
 * Human disease
 * DOID:6179
 * ovarian solid teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6315
 * ovarian squamous cell carcinoma
 * class of disease
 * ovarian squamous cell neoplasm squamous cell carcinoma ovarian cancer
 * Human disease
 * DOID:5531
 * ovarian squamous cell neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:5532
 * ovarian surface papilloma
 * class of disease
 * ovarian papillary neoplasm
 * Human disease
 * DOID:6407
 * ovary adenocarcinoma
 * class of disease
 * ovarian carcinoma adenocarcinoma
 * ovarian carcinoma that derives from epithelial cells of glandular origin
 * DOID:3713
 * Adenocarcinomas of the ovary
 * [[File:Metastatic ovarian adenocarcinoma- Pleural fluid cell block Case 168 (5494503444).jpg|center|64px]]
 * ovary leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5263
 * ovary mixed epithelial carcinoma
 * class of disease
 * ovarian carcinoma
 * Human disease
 * DOID:6898 DOID:6899
 * ovary neuroendocrine neoplasm
 * class of disease
 * ovarian cancer neuroendocrine tumor
 * Human disease
 * DOID:3002
 * ovary papillary carcinoma
 * class of disease
 * ovarian papillary neoplasm ovarian carcinoma
 * Human disease
 * DOID:6408
 * ovary rhabdomyosarcoma
 * class of disease
 * ovary sarcoma rhabdomyosarcoma
 * Human disease
 * DOID:4059
 * ovary sarcoma
 * class of disease
 * ovarian cancer sarcoma
 * human disease
 * DOID:2146
 * ovary serous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma ovarian serous carcinoma
 * ovary adenocarcinoma that derives from the lining of a cavity that produces a serum-like fluid (a serous cavity)
 * DOID:5744
 * Serous adenocarcinoma of the ovary
 * overhydrated hereditary stomatocytosis
 * class of disease
 * macrocytic anemia autosomal dominant disease hereditary stomatocytosis
 * human disease
 * DOID:0111562
 * overnutrition
 * class of disease
 * nutrition disorder malnutrition
 * form of malnutrition in which the intake of nutrients is oversupplied
 * DOID:654
 * C18.654.726
 * ovine and caprine brucellosis
 * class of disease
 * brucellosis
 * A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.
 * DOID:14456
 * oxirane allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger oxirane
 * DOID:0040082
 * oxyphilic adenoma
 * class of disease
 * endocrine organ benign neoplasm oncocytic neoplasm benign epithelial neoplasm disease
 * Human disease
 * DOID:5389
 * C04.557.470.035.140
 * Oncocytoma
 * Parotid gland oncocytoma - very high mag.jpg
 * oxyphilic endometrial endometrioid adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:6865
 * pain agnosia
 * class of disease
 * agnosia absence of pain sensation
 * agnosia that is a loss of the ability to perceive and process pain
 * DOID:0060145
 * pain disorder
 * class of disease
 * somatoform disorder disease pain
 * somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.
 * DOID:0060164
 * palindromic rheumatism
 * class of disease
 * syndrome arthritis
 * human disease
 * DOID:1166
 * palladium allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis metal allergy
 * allergic contact dermatitis that has allergic trigger palladium
 * DOID:0040055
 * palmoplantar keratosis
 * class of disease
 * keratosis foot diseases epidermal disease disease
 * keratosis characterized by abnormal thickening of the palms and the soles
 * DOID:3390
 * C16.320.850.475 C17.800.428.435 C17.800.827.475
 * Palmoplantar keratodermas
 * pancreas disease
 * class of disease
 * endocrine system disease
 * endocrine system disease that is located in the pancreas
 * DOID:26
 * C06.689
 * Diseases and disorders of pancreas
 * pancreas lymphoma
 * class of disease
 * pancreatic cancer lymphoma
 * human disease
 * DOID:1792
 * pancreas sarcoma
 * class of disease
 * pancreatic cancer sarcoma
 * pancreatic cancer that is located in the pancreas and that arises from transformed cells of mesenchymal origin
 * DOID:1796
 * pancreatic ACTH hormone producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:7697
 * pancreatic acinar cell adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma Acinar cell carcinoma of the pancreas acinar adenocarcinoma
 * pancreatic adenocarcinoma that has material basis in cells with morphological resemblance to acinar cells and is associated with increased serum lipase
 * DOID:5742
 * pancreatic adenocarcinoma
 * class of disease
 * pancreatic carcinoma adenocarcinoma
 * pancreatic carcinoma that derives from epithelial cells of glandular origin
 * DOID:4074
 * Adenocarcinomas of the pancreas
 * [[File:Metastatic pancreatic adenocarcinoma with lepidic growth pattern Case 280 (9840005374).jpg|center|64px]]
 * pancreatic cancer
 * class of disease
 * endocrine gland cancer pancreas disease pancreatic neoplasm gastrointestinal system cancer disease
 * endocrine gland cancer located in the pancreas
 * DOID:1793
 * Pancreatic cancer
 * MBq cystic-carcinoma-pancreas.jpg
 * pancreatic carcinoma
 * class of disease
 * pancreatic cancer carcinoma gastrointestinal carcinoma
 * pancreas cancer that derives from epithelial cells located in the pancreas
 * DOID:4905
 * pancreatic cholera
 * class of disease
 * endocrine pancreas disease
 * Human disease
 * DOID:6977
 * pancreatic colloid cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma mucinous cystadenocarcinoma
 * Human disease
 * DOID:7234
 * pancreatic cystadenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma cystadenocarcinoma
 * Human disease
 * DOID:4073
 * pancreatic cystadenoma
 * class of disease
 * benign neoplasm of exocrine pancreas endocrine organ benign neoplasm benign neoplasm of pancreas gastrointestinal system benign neoplasm pancreas disease
 * human disease
 * DOID:3918
 * pancreatic delta cell neoplasm
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:4433
 * pancreatic ductal adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * pancreatic adenocarcinoma that derives from pancreatic duct cells
 * DOID:3498
 * pancreatic ductal carcinoma
 * class of disease
 * pancreatic cancer ductal carcinoma pancreatic carcinoma
 * most common cancer of the pancreas
 * DOID:3587
 * C04.557.470.200.025.232.750 C04.557.470.615.132.750 C04.588.274.761.750 C04.588.322.475.750 C06.301.761.750 C06.689.667.625 C19.344.421.750
 * pancreatic foamy gland adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * Human disease
 * DOID:7577
 * pancreatic gastrinoma
 * class of disease
 * islet cell tumor functional pancreatic neuroendocrine tumor
 * Human disease
 * DOID:5580
 * pancreatic intraductal papillary-colloid carcinoma
 * class of disease
 * pancreatic adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7574
 * pancreatic intraductal papillary-mucinous adenoma
 * class of disease
 * pancreatic intraductal papillary-mucinous neoplasm adenoma of pancreas gastrointestinal system benign neoplasm adenoma
 * Human disease
 * DOID:7851
 * pancreatic intraductal papillary-mucinous neoplasm
 * class of disease
 * cancer of exocrine pancreas
 * Human disease
 * DOID:7575
 * pancreatic invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma
 * Human disease
 * DOID:8150
 * pancreatic invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * Human disease
 * DOID:7236
 * pancreatic mucinous cystadenoma
 * class of disease
 * mucinous cystadenoma pancreatic cystadenoma
 * human disease
 * DOID:7235
 * pancreatic mucinous ductal ectasia
 * class of disease
 * pancreas disease
 * Human disease
 * DOID:13313
 * pancreatic non-functioning delta cell tumor
 * class of disease
 * pancreatic delta cell neoplasm non-functioning pancreatic endocrine tumor
 * Human disease
 * DOID:7840
 * pancreatic non-invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7685
 * pancreatic non-invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * human disease
 * DOID:7237
 * pancreatic serous cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma serous cystadenocarcinoma pancreatic serous cystic neoplasm
 * Human disease
 * DOID:5751
 * pancreatic serous cystadenoma
 * class of disease
 * serous cystadenoma pancreatic cystadenoma disease
 * human disease
 * DOID:3917
 * Serous cystadenoma pancreas
 * pancreatic serous cystic neoplasm
 * class of disease
 * pancreatic exocrine neoplasm Serous tumour cystic lesions of the pancreas cancer of exocrine pancreas
 * Human disease
 * DOID:3919
 * Serous cystic neoplasms of the pancreas
 * pancreatic signet ring cell adenocarcinoma
 * class of disease
 * pancreatic ductal adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:3497
 * pancreatic solid pseudopapillary carcinoma
 * class of disease
 * pancreatic carcinoma
 * pancreatic carcinoma that is characterized by its papillary architecture
 * DOID:6827
 * pancreatic somatostatinoma
 * class of disease
 * islet cell tumor pancreatic delta cell neoplasm somatostatinoma
 * Human disease
 * DOID:4432
 * pancreatic squamous cell carcinoma
 * class of disease
 * pancreatic cancer squamous cell carcinoma
 * squamous cell carcinoma located in the pancreas
 * DOID:0080323
 * pancreatic steatorrhea
 * class of disease
 * pancreas disease steatorrhea
 * Human disease
 * DOID:10610
 * pancreatic vasoactive intestinal peptide producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:5741
 * pancreatoblastoma
 * class of disease
 * pancreatic carcinoma rare epithelial tumor of pancreas disease
 * Human disease
 * DOID:6823
 * pancytopenia
 * class of disease
 * anemia cytopenia disease
 * medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets
 * DOID:12450
 * C15.378.243.875
 * panhypopituitarism, X-linked
 * class of disease
 * panhypopituitarism X-linked disease
 * human disease
 * DOID:0111779
 * panic disorder
 * class of disease
 * anxiety disorder disease
 * anxiety disorder characterized by reoccurring unexpected panic attacks
 * DOID:594
 * F03.080.700
 * Panic disorder
 * Panic attack.jpg
 * panniculitis
 * class of disease
 * fibromyalgia connective tissue disease skin disease disease
 * Inflammation of the subcutaneous adipose tissue
 * DOID:1526
 * C17.300.710 C17.800.566
 * Panniculitis
 * An introduction to dermatology (1905) erythema induratum 2.jpg
 * panuveitis
 * class of disease
 * uveitis
 * Human disease
 * DOID:12030
 * C11.941.879.780
 * papillary adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue
 * DOID:3112
 * C04.557.470.200.025.085
 * papillary adenofibroma
 * class of disease
 * adenofibroma
 * biphasic polypoid neoplasm characterized by the presence of papillary projections that are lined by epithelial cells and fibrotic stroma
 * DOID:5479
 * papillary adenoma
 * class of disease
 * glandular cell epithelial neoplasm adenoma
 * Human disease
 * DOID:3172
 * papillary carcinoma
 * class of disease
 * carcinoma
 * carcinoma derived from epithelial cells with finger-like projections
 * DOID:3113
 * C04.557.470.200.360 C04.557.470.700.360
 * papillary conjunctivitis
 * class of disease
 * conjunctivitis
 * Human disease
 * DOID:2458
 * papillary craniopharyngioma
 * class of disease
 * craniopharyngioma
 * Human disease
 * DOID:3847
 * papillary cystadenocarcinoma
 * class of disease
 * cystadenocarcinoma papillary cystic tumor
 * cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with cysts and papillary endophytic projections
 * DOID:3110
 * C04.557.470.200.025.480.230 C04.557.470.590.480.230
 * papillary eccrine adenoma
 * class of disease
 * eccrine sweat gland neoplasm papillary adenoma
 * Human disease
 * DOID:5446
 * papillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5505
 * papillary extrahepatic bile duct adenocarcinoma
 * class of disease
 * extrahepatic bile duct adenocarcinoma
 * Human disease
 * DOID:6931
 * papillary follicular thyroid adenocarcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:3968
 * C04.557.470.200.025.060.225 C04.557.470.200.025.085.225
 * papillary hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:5439
 * Papillary hidradenoma
 * Papillary hidradenoma - very high mag.jpg
 * papillary meningioma of the cerebellum
 * class of disease
 * cerebellum cancer rhabdoid meningioma papillary meningioma brain meningioma
 * Human disease
 * DOID:5057
 * papillary pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8193
 * papillary renal cell carcinomas
 * class of disease
 * renal cell carcinoma
 * renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors
 * DOID:4465
 * [[File:Histopathology of papillary renal cell carcinoma type 1, grade 2, with variable density.jpg|center|64px]]
 * papillary serous adenocarcinoma
 * class of disease
 * papillary adenocarcinoma
 * papillary adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures with psammoma bodies
 * DOID:2632
 * papillary squamous carcinoma
 * class of disease
 * squamous cell carcinoma papillary carcinoma
 * Human disease
 * DOID:4385
 * papillary thymic adenocarcinoma
 * class of disease
 * thymus adenocarcinoma
 * Human disease
 * DOID:5595
 * papillary thyroid cancer
 * class of disease
 * thyroid carcinoma papillary carcinoma differentiated thyroid carcinoma
 * thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer
 * DOID:3969
 * C04.557.470.200.025.085.612 C04.588.322.894.400 C04.588.443.915.400 C19.344.894.400 C19.874.788.400
 * Thyroid papillary carcinoma
 * papillary transitional carcinoma
 * class of disease
 * transitional cell carcinoma
 * transitional cell carcinoma that has several papillary fronds with central fibrovascular core lined by transitional type epithelium
 * DOID:4012
 * Urothelial papillary carcinoma
 * papillary urothelial neoplasm of low malignant potential
 * class of disease
 * bladder papillary transitional cell neoplasm urinary tract non-invasive transitional cell neoplasm papillary urothelial lesion
 * human disease
 * DOID:6239
 * papilledema
 * class of disease
 * optic nerve disease disease
 * Human disease
 * DOID:146
 * C10.292.700.900 C11.640.710
 * Papilledema
 * Papilledema.jpg
 * papilloma
 * class of disease
 * benign neoplasms by histologic type papillary tumor disease
 * cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue
 * DOID:2615
 * C04.557.470.700.600
 * Papillomas
 * parachordoma
 * class of disease
 * mesenchymal cell neoplasm
 * Human disease
 * DOID:2647
 * paralytic ileus
 * class of disease
 * bowel obstruction ileus
 * Human disease
 * DOID:8442
 * Paralytic ileus
 * paralytic lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:12958
 * paralytic poliomyelitis
 * class of disease
 * poliomyelitis central nervous system disease
 * Human disease
 * DOID:0050515
 * paralytic squint
 * class of disease
 * strabismus cranial nerve palsy
 * Human disease
 * DOID:10863
 * parameningeal embryonal rhabdomyosarcoma
 * class of disease
 * embryonal rhabdomyosarcoma
 * embryonal rhabdomyosarcoma located in the parameningeal region
 * DOID:0060338
 * parametritis
 * class of disease
 * pelvic inflammatory diseases inflammatory disease uterine disease
 * Human disease
 * DOID:1260
 * C13.351.500.056.750.750
 * parametrium malignant neoplasm
 * class of disease
 * uterine adnexa cancer broad ligament malignant neoplasm
 * Human disease
 * DOID:11746
 * paramyotonia congenita of Von Eulenburg
 * class of disease
 * neuromuscular disease autosomal dominant disease paramyotonia congenita
 * human disease
 * DOID:0111538
 * paranasal sinus disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:1352
 * C08.460.692 C09.603.692
 * paranasal sinus lymphoma
 * class of disease
 * paranasal sinus cancer lymphoma
 * human disease
 * DOID:1355
 * paranasal sinus neoplasm
 * class of disease
 * respiratory tract neoplasm paranasal sinus disease respiratory system benign neoplasm
 * human disease
 * DOID:1350
 * C04.588.443.665.650.693 C08.460.669.693 C08.460.692.503 C08.785.600.693 C09.603.669.693 C09.603.692.503 C09.647.685.693
 * Neoplasms of paranasal sinuses
 * paranasal sinus sarcoma
 * class of disease
 * paranasal sinus cancer sarcoma
 * sarcoma and malignant tumor of nasal sinuses that is located in the paranasal sinus
 * DOID:1362
 * paraneoplastic pemphigus
 * class of disease
 * pemphigus
 * human disease
 * DOID:0080852
 * paraneoplastic polyneuropathy
 * class of disease
 * inflammatory and toxic neuropathy peripheral neuropathy paraneoplastic neurologic syndrome
 * Human disease
 * DOID:8681
 * C04.588.614.550.700 C04.730.856.700 C10.574.781.850 C10.668.829.800.662
 * paranoid personality disorder
 * class of disease
 * personality disorder disease
 * mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others
 * DOID:10938
 * F03.675.600
 * Paranoid personality disorder
 * parapharyngeal meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:8216
 * paraphilia
 * class of disease
 * psychosexual disorder sexual and gender disorder disease
 * experience of intense sexual arousal to atypical objects, situations, or individuals
 * DOID:0060044
 * F03.657
 * Paraphilias
 * Martin van Maele - La Comtesse au fouet 01.jpg
 * paraphimosis
 * class of disease
 * phimosis disease
 * medical condition in which the foreskin of a penis becomes trapped behind the glans penis
 * DOID:5334
 * C12.294.494.684.587
 * Paraphimosis
 * Paraphimosis.jpg
 * paraplegia
 * class of disease symptom or sign
 * central nervous system disease paralysis disease
 * impairment in motor or sensory function of the lower extremities
 * DOID:607
 * C10.597.622.669 C23.888.592.636.637
 * Paraplegia
 * parapsoriasis
 * class of disease
 * psoriasis disease
 * Human disease
 * DOID:9088
 * C17.800.859.575
 * parasagittal meningioma
 * class of disease
 * cerebral convexity meningioma
 * Human disease
 * DOID:6869
 * parasitic Ichthyosporea infectious disease
 * class of disease
 * parasitic infectious diseases
 * parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals
 * DOID:0050291
 * C03.600
 * parasitic conjunctivitis
 * class of disease
 * chronic conjunctivitis parasitic eye infection
 * Human disease
 * DOID:13341
 * parasitic eyelid infestation
 * class of disease
 * blepharitis parasitic eye infection
 * Human disease
 * DOID:13823
 * parasitic protozoa infectious disease
 * class of disease
 * parasitic infectious diseases disease
 * parasitic disease caused by a protozoan
 * DOID:2789
 * C01.610.752
 * paratesticular lipoma
 * class of disease
 * reproductive organ benign neoplasm lipoma
 * Human disease
 * DOID:10207
 * parathyroid adenoma
 * class of disease
 * parathyroid neoplasm benign parathyroid gland neoplasm benign neoplasms by histologic type adenoma disease
 * Human disease
 * DOID:7608
 * Parathyroid adenoma
 * parathyroid gland disease
 * class of disease
 * endocrine system disease
 * endocrine disease
 * DOID:11201
 * C19.642
 * parathyroid oncocytic adenoma
 * class of disease
 * parathyroid adenoma oxyphilic adenoma
 * Human disease
 * DOID:7611
 * parathyroid transitional clear cell adenoma
 * class of disease
 * parathyroid adenoma
 * Human disease
 * DOID:7609
 * paraurethral gland cancer
 * class of disease
 * female reproductive organ cancer paraurethral gland neoplasm
 * Human disease
 * DOID:14059
 * paraurethral gland neoplasm
 * class of disease
 * urethral benign neoplasm
 * Human disease
 * DOID:2139
 * parenchymatous neurosyphilis
 * class of disease
 * tertiary neurosyphilis
 * Human disease
 * DOID:0050490
 * parietal lobe ependymoma
 * class of disease
 * parietal lobe malignant neoplasm ependymoma
 * parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain
 * DOID:0050903
 * paronychia
 * class of disease
 * nail disease disease
 * bacterial or fungal nail infection of the hand or foot
 * DOID:13117
 * C01.539.800.460 C17.800.529.639 C17.800.838.486
 * Paronychia (disease)
 * Paronychia.jpg
 * parotid disease
 * class of disease
 * salivary gland disease
 * Human disease
 * DOID:10302
 * C07.465.815.470
 * Diseases and disorders of parotid glands
 * parotitis
 * class of disease
 * parotid disease inflammatory disease sialadenitis disease
 * parotid disease characterized by the inflammation of one or both parotid glands
 * DOID:10301
 * C07.465.815.470.800 C07.465.815.793.500
 * parovarian cyst
 * class of disease
 * female reproductive system disease embryonic cyst of fallopian tube
 * Human disease
 * DOID:4333
 * C04.182.668 C23.300.306.500
 * paroxysmal nonkinesigenic dyskinesia 2
 * class of disease
 * Paroxysmal dyskinesia dystonia genetic disease
 * human disease
 * DOID:0090047
 * pars planitis
 * class of disease
 * intermediate uveitis chorioretinitis ciliary body disease rare genetic eye disease disease
 * Human disease
 * DOID:12731
 * C11.941.160.478.700 C11.941.879.780.900.300.659 C11.941.879.900.500
 * parthenolide allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger parthenolide
 * DOID:0040072
 * partial androgen insensitivity syndrome
 * class of disease
 * X-linked recessive disease androgen insensitivity syndrome
 * medical condition
 * DOID:0080776
 * partial arterial retinal occlusion
 * class of disease
 * retinal artery occlusion
 * Human disease
 * DOID:14522
 * partial circumpapillary choroid dystrophy
 * class of disease
 * hereditary choroidal atrophy
 * human disease
 * DOID:9811
 * partial lipodystrophy
 * class of disease
 * lipodystrophy
 * lipodystrophy that is characterized by partial loss of adipose tissue
 * DOID:0080299
 * partial motor epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3327
 * C10.228.140.490.360.272
 * partial optic atrophy
 * class of disease
 * optic atrophy
 * human disease
 * DOID:10631
 * partial pancreatic agenesis
 * class of disease
 * pancreas disease agenesis pancreatic agenesis
 * pancreas disease that is characterized by the failure of the pancreas to develop prior to birth
 * DOID:0050877
 * partial retinal vein occlusion
 * class of disease
 * retinal vein occlusion
 * Human disease
 * DOID:1726
 * partial sensory epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3330
 * C10.228.140.490.360.275
 * partial third-nerve palsy
 * class of disease
 * paralytic squint oculomotor nerve paralysis
 * Human disease
 * DOID:10864
 * patellar tendinitis
 * class of disease
 * tendinitis knee disorder knee extensor tendonitis
 * Human disease
 * DOID:10471
 * Patellar tendinitis
 * patent blue V allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger patent blue V
 * DOID:0040080
 * paternal uniparental disomy of chromosome 14
 * class of disease
 * uniparental disomy of paternal origin uniparental disomy 14 syndrome
 * human disease
 * DOID:0111712
 * pathologic nystagmus
 * class of disease
 * nystagmus ocular motility disease abnormal eye movements
 * Human disease
 * DOID:9650
 * C10.292.562.675 C11.590.400
 * patterned macular dystrophy 1
 * class of disease
 * patterned macular dystrophy
 * human disease
 * DOID:0060866
 * patulous eustachian tube
 * class of disease physiological condition
 * eustachian tube disease
 * eustachian tube disorder
 * DOID:12358
 * peach allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus persica plant fruit food product.
 * DOID:0060510
 * peanut allergy
 * class of disease
 * tree nut allergy legume allergy vegetable allergy
 * type of food allergy caused by peanuts
 * DOID:4378
 * C20.543.480.370.572.750
 * Nut warning 1.jpg
 * pediatric CNS choriocarcinoma
 * class of disease
 * malignant childhood germ cell neoplasm central nervous system choriocarcinoma rare childhood malignant neoplasm choriocarcinoma
 * Human disease
 * DOID:6639
 * pediatric CNS embryonal cell carcinoma
 * class of disease
 * central nervous system childhood germ cell tumor central nervous system embryonal carcinoma rare childhood malignant neoplasm malignant childhood germ cell neoplasm brain cancer
 * Human disease
 * DOID:7231
 * pediatric angiosarcoma
 * class of disease
 * angiosarcoma rare childhood malignant neoplasm
 * angiosarcoma that affects children
 * DOID:4505
 * pediatric cerebral ependymoblastoma
 * class of disease
 * ependymoblastoma
 * Human disease
 * DOID:7841
 * pediatric ependymoma
 * class of disease
 * ependymoma childhood cancer ependymal tumor childhood neoplasm
 * human disease
 * DOID:5509
 * pediatric epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7095
 * pediatric fibrosarcoma
 * class of disease
 * fibrosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3520
 * pediatric germ cell tumor
 * class of disease
 * germ cell tumor childhood neoplasm
 * Human disease
 * DOID:6053
 * pediatric hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma childhood cancer of liver
 * Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age
 * DOID:0070322
 * pediatric infratentorial ependymoblastoma
 * class of disease
 * childhood infratentorial neoplasm ependymoblastoma infratentorial cancer childhood central nervous system primitive neuroectodermal neoplasm rare childhood malignant neoplasm
 * Human disease
 * DOID:7522
 * pediatric infratentorial ependymoma
 * class of disease
 * infratentorial cancer pediatric ependymoma brain ependymoma childhood infratentorial neoplasm childhood cancer
 * Human disease
 * DOID:7501
 * pediatric leptomeningeal melanoma
 * class of disease
 * meningeal melanoma
 * Human disease
 * DOID:6089
 * pediatric liposarcoma
 * class of disease
 * liposarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5695
 * pediatric low-grade glioma
 * class of disease
 * low grade glioma
 * human disease
 * DOID:0080830
 * pediatric lymphoma
 * class of disease
 * lymphoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5823
 * pediatric meningioma
 * class of disease
 * meningioma pediatric central nervous system tumor
 * Human disease
 * DOID:4593
 * pediatric mesenchymal chondrosarcoma
 * class of disease
 * mesenchymal chondrosarcoma childhood cancer
 * Human disease
 * DOID:4546
 * pediatric myxoid chondrosarcoma
 * class of disease
 * myxoid chondrosarcoma childhood cancer
 * Human disease
 * DOID:6494
 * pediatric osteosarcoma
 * class of disease
 * osteosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3361
 * pediatric ovarian dysgerminoma
 * class of disease
 * pediatric ovarian germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm dysgerminoma of ovary
 * dysgerminoma of ovary that occurs in children
 * DOID:7340
 * pediatric ovarian germ cell tumor
 * class of disease
 * ovarian germ cell neoplasm pediatric germ cell tumor
 * Human disease
 * DOID:6084
 * pediatric supratentorial ependymoma
 * class of disease
 * supratentorial cancer pediatric ependymoma brain ependymoma
 * Human disease
 * DOID:7502
 * pediatric testicular germ cell tumor
 * class of disease
 * testicular germ cell tumor pediatric germ cell tumor
 * Human disease
 * DOID:6082
 * peliosis hepatis
 * class of disease
 * hepatic vascular disease
 * Human disease
 * DOID:914
 * C06.552.802
 * Peliosis hepatis
 * pellagra
 * class of disease
 * nutritional deficiency disease other acquired skin disease skin disease disease
 * Human disease
 * DOID:8457
 * C18.654.521.500.133.699.529
 * Pellagra
 * Pellagra NIH.jpg
 * pelvic inflammatory diseases
 * class of disease
 * female reproductive system disease adnexal disease infectious disease disease
 * infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis
 * DOID:1003
 * C01.635.500 C12.050.351.500.056.750 C12.100.250.056.750
 * Pelvic inflammatory disease
 * Blausen 0732 PID-Sites.png
 * pelvic lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3927
 * pelvic muscle wasting
 * class of disease
 * pelvic organ prolapse pelvic floor dysfunction
 * Human disease
 * DOID:11629
 * pelvic organ prolapse
 * class of disease
 * female reproductive system disease prolapse
 * pelvic organs protruding from the opening of the vagina
 * DOID:1284
 * C23.300.842.624
 * Female genital prolapse
 * Hippocrates treatment for prolapse.png
 * pelvic varices
 * class of disease
 * varicose veins
 * Human disease
 * DOID:9742
 * pemphigoid
 * class of disease
 * autoimmune skin disease bullous skin disease
 * human disease
 * DOID:0080841
 * penicillin drug reaction
 * class of disease
 * adverse drug reaction beta-lactam allergy Side effects of penicillin
 * beta-lactam allergy triggered by penicillin
 * DOID:0060520
 * penicilliosis
 * class of disease
 * opportunistic mycosis disease
 * Human disease
 * DOID:0050288
 * penile cancer
 * class of disease
 * penile neoplasm male reproductive organ cancer penile disease disease
 * cancer of the penis
 * DOID:11615
 * Penile cancer
 * Penile cancer 2.jpg
 * penile disease
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:1529
 * C12.294.494
 * penile neoplasm
 * class of disease
 * male reproductive system neoplasm penile disease male reproductive organ benign neoplasm
 * human disease
 * DOID:11624
 * C04.588.945.440.715 C12.294.260.500 C12.294.494.591 C12.758.409.500
 * Penile neoplasms
 * penile urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8223
 * penis Paget's disease
 * class of disease
 * penis carcinoma extramammary Paget's disease adenocarcinoma of penis genetic urogenital tumor
 * Human disease
 * DOID:3448
 * Penile Paget's disease
 * penis basal cell carcinoma
 * class of disease
 * penis carcinoma basal-cell carcinoma rare skin disease
 * human disease
 * DOID:4277
 * penis basaloid carcinoma
 * class of disease
 * penis squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7047
 * penis carcinoma
 * class of disease
 * penile cancer carcinoma
 * penile cancer that is located in the skin or tissues of the penis
 * DOID:3449
 * penis carcinoma in situ
 * class of disease
 * in situ carcinoma penile disease penis squamous cell carcinoma carcinoma in situ of male genital organs
 * Human disease
 * DOID:8872
 * penis mixed squamous cell carcinoma
 * class of disease
 * penis squamous cell carcinoma
 * Human disease
 * DOID:8009
 * penis non-invasive verrucous carcinoma
 * class of disease
 * penis verrucous carcinoma penis carcinoma in situ cervical verrucous carcinoma
 * Human disease
 * DOID:5907
 * penis papillary carcinoma
 * class of disease
 * penis squamous cell carcinoma papillary squamous carcinoma
 * Human disease
 * DOID:8013
 * penis sarcoma
 * class of disease
 * penile cancer sarcoma
 * sarcoma and malignant neoplasm of penis that is located in the penis
 * DOID:11838
 * penis squamous cell carcinoma
 * class of disease
 * penis carcinoma squamous cell carcinoma
 * penis carcinoma that has material basis in squamous cells
 * DOID:5518
 * Squamous-cell carcinoma of the penis
 * penis verrucous carcinoma
 * class of disease
 * penis squamous cell carcinoma verrucous carcinoma penis papillary carcinoma
 * Human disease
 * DOID:5908
 * peptic esophagitis
 * class of disease
 * peptic ulcer disease esophagitis gastroesophageal reflux disease
 * human disease
 * DOID:13976
 * C06.405.117.620.420 C06.405.205.663.420 C06.405.469.275.800.523 C06.405.748.586.524
 * peptic ulcer disease
 * class of disease
 * gastrointestinal system disease duodenal disease disease
 * ulcer of an area of the gastrointestinal tract
 * DOID:750
 * C06.405.469.275.800 C06.405.748.586
 * Peptic ulcers
 * Benign gastric ulcer 1.jpg
 * perforated corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10445
 * perforated ulcer
 * class of disease
 * peptic ulcer disease gastric perforation
 * medical condition of the gastrointestinal tract wall
 * DOID:752
 * C06.405.469.275.800.698 C06.405.748.586.698
 * DU 2.jpg
 * perforation of bile duct
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:13409
 * periampullary adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma
 * Human disease
 * DOID:8110
 * periampullary adenoma
 * class of disease
 * ampulla of Vater neoplasm adenoma
 * Human disease
 * DOID:0050849
 * perianal gland tumor
 * class of disease
 * cancer in dogs anus neoplasm
 * dog disease
 * DOID:4550
 * C04.588.083 C04.588.274.476.411.307.790.040.040 C06.301.371.411.307.790.040.040 C06.405.249.411.307.790.040.040 C06.405.469.491.307.790.040.040 C06.405.469.860.101.163.083 C06.405.469.860.180.500.040.040 C22.073
 * perianal hematoma
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9745
 * Perianal hematoma
 * perianal skin Paget's disease
 * class of disease
 * anal margin carcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:7708
 * periapical abscess
 * class of disease
 * periapical periodontitis dental abscess
 * localized collection of pus associated with a tooth
 * DOID:2562
 * C01.539.830.025.650 C07.320.830.700.700 C07.465.714.306.700.700 C07.465.714.533.487.700
 * periapical periodontitis
 * class of disease
 * inflammation periodontitis dental pulp disease periapical disease tooth pathology
 * Human disease
 * DOID:823
 * C07.320.830.700 C07.465.714.306.700 C07.465.714.533.487
 * pericardial effusion
 * class of disease symptom or sign
 * pericardium disease cardiovascular system symptom disease
 * pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
 * DOID:118
 * C14.280.695
 * Pericardial effusion
 * pericardial mesothelioma
 * class of disease
 * pericardium cancer mesothelioma
 * Human disease
 * DOID:6201
 * pericarditis
 * class of disease
 * pericardium disease inflammation inflammatory disease heart disease disease
 * pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
 * DOID:1787
 * C14.280.720
 * Pericarditis
 * Pericarditis10.JPG
 * pericardium cancer
 * class of disease
 * heart cancer neoplasm of pericardium pericardium disease
 * Human disease
 * DOID:116
 * pericardium leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of pericardium pericardium disease cardiovascular organ benign neoplasm
 * Human disease
 * DOID:5137
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * osteoclast-like giant cell neoplasm of the pancreas
 * class of disease
 * pancreatic ductal adenocarcinoma undifferentiated pancreatic carcinoma
 * Human disease
 * DOID:7718
 * osteogenesis imperfecta 21
 * class of disease
 * osteogenesis imperfecta
 * human disease
 * DOID:0112201
 * osteogenesis imperfecta type 1
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by bone fragility and blue sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110334
 * osteogenesis imperfecta type 16
 * class of disease
 * osteogenesis imperfecta
 * osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
 * DOID:0110345
 * osteogenesis imperfecta type 18
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111848
 * osteogenesis imperfecta type 20
 * class of disease
 * autosomal recessive disease osteogenesis imperfecta
 * human disease
 * DOID:0111849
 * osteogenesis imperfecta type 3
 * class of disease
 * osteogenesis imperfecta genetic disease autosomal dominant disease
 * An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has material basis in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
 * DOID:0110339
 * osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
 * class of disease
 * osteogenesis imperfecta dentinogenesis imperfecta blue sclera
 * osteogenesis imperfecta found in a single South African family
 * DOID:0110335
 * osteomalacia
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone
 * DOID:10573
 * C05.116.198.816.640 C18.452.104.816.640 C18.452.174.845.640 C18.654.521.500.133.770.734.640
 * Calcitriol.svg
 * osteomyelitis
 * class of disease
 * bone inflammation disease infectious disease disease
 * bone inflammation disease that has material basis in infection located in bone or located in bone marrow
 * DOID:1019
 * C01.160.495 C05.116.165.495
 * Osteomyelitis
 * osteonecrosis
 * class of disease symptom or sign
 * necrosis ischemic bone disease disease
 * bone death caused when the bone no longer receives blood supply
 * DOID:10159
 * C05.116.852 C23.550.717.732
 * Aseptic osteonecrosis
 * Head of femur avascular necrosis.jpg
 * osteopoikilosis
 * class of disease
 * osteosclerosis
 * osteosclerosis that results in numerous bone islands located in skeleton
 * DOID:11991
 * C05.116.099.708.702.685 C17.300.705
 * Osteopoikilosis
 * osteoporosis
 * class of disease
 * bone resorption disease disease
 * bone resorption disease characterized by the thinning of bone tissue and decreased mechanical strength
 * DOID:11476
 * C05.116.198.579 C18.452.104.579
 * Osteoporosis
 * Osteoporosis -- Smart-Servier.jpg
 * osteosarcoma
 * class of disease
 * bone cancer cell type cancer bone sarcoma osteogenic neoplasm disease childhood cancer
 * bone cancer that is located in bone that has material basis in cells of mesenchymal origin
 * DOID:3347
 * C04.557.450.565.575.650 C04.557.450.795.620
 * Osteosarcoma
 * Osteosarcoma.jpg
 * osteosarcoma arising in bone Paget's disease
 * class of disease
 * bone osteosarcoma mammary Paget's disease
 * Human disease
 * DOID:7542
 * osteosclerosis
 * class of disease
 * bone remodeling disease disease
 * bone remodeling disease that results in abnormal elevated bone density or mass
 * DOID:4254
 * C05.116.099.708.702
 * ScleroticmetastaticdiseasePelvis.png
 * otomycosis
 * class of disease symptom or sign
 * otitis externa dermatomycosis disease
 * human disease
 * DOID:0050147
 * C01.150.703.658 C09.218.736
 * Otomycosis
 * Otomycosis.jpg
 * otopalatodigital syndrome spectrum disorder
 * class of disease
 * bone development disease
 * DOID:0111782
 * otosclerosis
 * class of disease
 * inner ear disease disease
 * otitis interna characterized by an abnormal bone growth in the middle ear
 * DOID:12185
 * C09.218.768
 * Otosclerosis
 * Gray919.png
 * otospondylomegaepiphyseal dysplasia, autosomal dominant
 * class of disease
 * osteochondrodysplasia autosomal dominant disease
 * human disease
 * DOID:0080677
 * outlet dysfunction constipation
 * class of disease
 * constipation
 * Human disease
 * DOID:2088
 * ovarian Brenner tumor
 * class of disease
 * ovarian benign neoplasm
 * ovarian benign neoplasm that has material basis in the surface epithelium of the ovary
 * DOID:2636
 * Brenner tumour
 * ovarian Wilms' cancer
 * class of disease
 * ovarian cancer
 * malignant neoplasm of ovary and nephroblastoma that is located in the ovaries
 * DOID:2153
 * ovarian angiosarcoma
 * class of disease
 * angiosarcoma ovary sarcoma sarcoma ovarian cancer
 * human disease
 * DOID:4527
 * ovarian benign neoplasm
 * class of disease
 * female reproductive organ benign neoplasm ovarian neoplasm endocrine organ benign neoplasm ovarian disease
 * human disease
 * DOID:0060112
 * Benign neoplasms of the ovary
 * ovarian biphasic or triphasic teratoma
 * class of disease
 * ovarian germ cell teratoma
 * Human disease
 * DOID:6232
 * ovarian cancer
 * class of disease
 * female reproductive organ cancer ovarian neoplasm ovarian disease endocrine gland cancer rare genetic endocrine disease inherited gynecological tumor disease
 * female reproductive organ cancer that is located in the ovary
 * DOID:2394
 * Ovarian cancer
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian carcinoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinoma
 * human disease
 * DOID:4001
 * ovarian carcinosarcoma
 * class of disease
 * malignant ovarian surface epithelial-stromal neoplasm carcinosarcoma mixed Müllerian tumor
 * Human disease
 * DOID:6170
 * ovarian clear cell adenocarcinoma
 * class of disease
 * ovary adenocarcinoma clear cell adenocarcinoma
 * Human disease
 * DOID:5304
 * ovarian clear cell adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5897
 * ovarian clear cell cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma ovarian clear cell adenocarcinoma
 * Human disease
 * DOID:7438
 * ovarian clear cell cystadenofibroma
 * class of disease
 * ovarian clear cell adenofibroma clear cell cystadenofibroma
 * Human disease
 * DOID:5896
 * ovarian clear cell malignant adenofibroma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:6554
 * ovarian cyst
 * class of disease
 * ovarian disease ovarian neoplasm disease
 * fluid-filled sac in the ovary
 * DOID:5119
 * C04.182.612 C13.351.500.056.630.580 C19.391.630.580
 * Ovarian cysts
 * Benign Ovarian Cyst.jpg
 * ovarian cystadenocarcinoma
 * class of disease
 * ovary adenocarcinoma cystadenocarcinoma ovarian cystadenoma
 * human disease
 * DOID:3605
 * ovarian cystadenoma
 * class of disease
 * ovarian benign neoplasm benign epithelial neoplasm
 * human disease
 * DOID:3269
 * ovarian cystic teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:5118
 * Mature cystic teratoma of ovary
 * ovarian disease
 * class of disease
 * female reproductive system disease gonadal disease adnexal disease
 * Human disease
 * DOID:1100
 * C13.351.500.056.630 C19.391.630
 * Diseases and disorders of ovaries
 * ovarian dysfunction
 * class of disease
 * ovarian disease
 * Human disease
 * DOID:1414
 * ovarian dysgenesis 1
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16
 * DOID:0080493
 * ovarian dysgenesis 4
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MCM9 gene on chromosome 6q22
 * DOID:0080496
 * ovarian dysgenesis 5
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the SOHLH1 gene on chromosome 9q34
 * DOID:0080497
 * ovarian dysgenesis 6
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the NUP107 gene on chromosome 12q15
 * DOID:0080498
 * ovarian dysgenesis 7
 * class of disease
 * autosomal recessive disease 46 XX gonadal dysgenesis
 * 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MRPS22 gene on chromosome 3q23
 * DOID:0080499
 * ovarian dysgenesis 8
 * class of disease
 * 46 XX gonadal dysgenesis autosomal dominant disease
 * 46 XX gonadal dysgenesis that has material basis in heterozygous mutation in the ESR2 gene on chromosome 14q23
 * DOID:0080500
 * ovarian embryonal carcinoma
 * class of disease
 * embryonal carcinoma malignant non-dysgerminomatous germ cell tumor of ovary ovarian cancer
 * embryonal carcinoma that is located in the ovary
 * DOID:5681
 * ovarian endodermal sinus tumor
 * class of disease
 * ovarian primitive germ cell tumor malignant non-dysgerminomatous germ cell tumor of ovary endodermal sinus tumor
 * Human disease
 * DOID:5350
 * ovarian endometrial cancer
 * class of disease
 * surface epithelial-stromal tumor Endometrioid tumor female reproductive endometrioid cancer
 * ovary epithelial cancer that has material basis in the endometrium and is located in the ovary
 * DOID:6212
 * ovarian endometrioid adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * Human disease
 * DOID:5480
 * ovarian endometrioid cystadenofibroma
 * class of disease
 * ovarian endometrioid adenofibroma cystadenofibroma
 * Human disease
 * DOID:7411
 * ovarian endometrioid cystadenoma
 * class of disease
 * ovarian cystadenoma
 * Human disease
 * DOID:7191
 * ovarian endometrioid malignant adenofibroma
 * class of disease
 * ovarian carcinosarcoma malignant adenofibroma
 * Human disease
 * DOID:6445
 * ovarian endometrioid stromal sarcoma
 * class of disease
 * ovary sarcoma
 * Human disease
 * DOID:5169
 * ovarian fetiform teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6314
 * ovarian germ cell monodermal and highly specialized teratoma
 * class of disease
 * monodermal teratoma
 * Human disease
 * DOID:2641
 * ovarian germ cell neoplasm
 * class of disease
 * ovarian neoplasm germ cell tumor germ cell and embryonal neoplasms ovarian cancer
 * benign or malignant ovarian tumor that originates in the germ (egg) cells of the ovary
 * DOID:2156
 * Germ cell neoplasms
 * ovarian germ cell teratoma
 * class of disease
 * ovarian germ cell neoplasm teratoma gonadal teratoma female reproductive organ cancer
 * Human disease
 * DOID:5567
 * Ovarian teratomas
 * Teratoma Ovary 4x.jpg
 * ovarian gonadoblastoma
 * class of disease
 * ovarian benign neoplasm gonadoblastoma
 * Human disease
 * DOID:3578
 * ovarian large-cell neuroendocrine carcinoma
 * class of disease
 * ovarian carcinoma familiar ovarian carcinoma inherited neuroendocrine tumor large cell neuroendocrine carcinoma
 * Human disease
 * DOID:4555
 * ovarian lymphoma
 * class of disease
 * ovarian cancer lymphoma
 * Human disease
 * DOID:2150
 * ovarian malignant mesothelioma
 * class of disease
 * ovarian cancer
 * Human disease
 * DOID:2143
 * ovarian melanoma
 * class of disease
 * ovarian cancer
 * ovarian cancer that has material basis in melanoctyes
 * DOID:0050928
 * ovarian mesodermal adenosarcoma
 * class of disease
 * ovarian carcinosarcoma adenosarcoma
 * adenosarcoma and malignant ovarian endometroid tumorthat is located in the ovary
 * DOID:4115
 * ovarian mixed germ cell neoplasm
 * class of disease
 * ovarian primitive germ cell tumor mixed germ cell cancer
 * Human disease
 * DOID:5936
 * ovarian mucinous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma malignant ovarian mucinous tumor mucinous adenocarcinoma
 * human disease
 * DOID:3606
 * ovarian mucinous adenofibroma
 * class of disease
 * ovarian benign neoplasm
 * human disease
 * DOID:6469
 * ovarian mucinous cystadenocarcinoma
 * class of disease
 * ovarian cystadenocarcinoma mucinous cystadenocarcinoma ovarian mucinous adenocarcinoma
 * Human disease
 * DOID:3604
 * ovarian mucinous cystadenofibroma
 * class of disease
 * ovarian mucinous adenofibroma mucinous cystadenofibroma
 * Human disease
 * DOID:7013
 * ovarian mucinous malignant adenofibroma
 * class of disease
 * malignant ovarian mucinous tumor malignant adenofibroma ovarian mucinous neoplasm
 * Human disease
 * DOID:6278
 * ovarian mucinous neoplasm
 * class of disease
 * surface epithelial-stromal tumor mucinous tumor
 * Human disease
 * DOID:6067
 * Ovarian mucinous tumors
 * Mucinous lmp ovarian tumour intermed mag.jpg
 * ovarian papillary cystadenoma
 * class of disease
 * ovarian papillary neoplasm papillary adenoma ovarian cystadenoma
 * Human disease
 * DOID:6405
 * ovarian papillary neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:6214
 * ovarian primitive germ cell tumor
 * class of disease
 * malignant ovarian germ cell neoplasm
 * Human disease
 * DOID:5351
 * ovarian serous adenofibroma
 * class of disease
 * ovarian benign neoplasm serous adenofibroma
 * Human disease
 * DOID:5474
 * ovarian serous carcinoma
 * class of disease
 * ovarian carcinoma serous carcinoma ovarian serous tumor
 * ovarian carcinoma that has material basis in the lining of the ovary and produces a serum-like fluid
 * DOID:0050933
 * Ovarian serous carcinoma
 * ovarian serous cystadenofibroma
 * class of disease
 * ovarian serous adenofibroma cystadenofibroma
 * Human disease
 * DOID:7320
 * ovarian serous cystadenoma
 * class of disease
 * serous cystadenoma ovarian benign neoplasm ovarian cystadenocarcinoma serous cystadenocarcinoma ovarian cystadenoma ovarian serous tumor
 * ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed
 * DOID:5746 DOID:3914
 * C04.557.470.035.320.240 C04.557.470.590.485.240
 * Ovarian serous cystadenoma
 * Ovarian serous cystadenoma - alt -- low mag.jpg
 * ovarian sex cord-stromal tumor
 * class of disease
 * sex cord-gonadal stromal tumor
 * A benign or malignant neoplasm that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts. Representative examples include thecoma, fibroma, Sertoli cell tumor, and granulosa cell tumor.
 * DOID:0080369
 * ovarian small cell carcinoma
 * class of disease
 * ovarian carcinoma small cell carcinoma
 * Human disease
 * DOID:6179
 * ovarian solid teratoma
 * class of disease
 * mature teratoma of the ovary
 * Human disease
 * DOID:6315
 * ovarian squamous cell carcinoma
 * class of disease
 * ovarian squamous cell neoplasm squamous cell carcinoma ovarian cancer
 * Human disease
 * DOID:5531
 * ovarian squamous cell neoplasm
 * class of disease
 * surface epithelial-stromal tumor
 * Human disease
 * DOID:5532
 * ovarian surface papilloma
 * class of disease
 * ovarian papillary neoplasm
 * Human disease
 * DOID:6407
 * ovary adenocarcinoma
 * class of disease
 * ovarian carcinoma adenocarcinoma
 * ovarian carcinoma that derives from epithelial cells of glandular origin
 * DOID:3713
 * Adenocarcinomas of the ovary
 * [[File:Metastatic ovarian adenocarcinoma- Pleural fluid cell block Case 168 (5494503444).jpg|center|64px]]
 * ovary leiomyosarcoma
 * class of disease
 * leiomyosarcoma
 * Human disease
 * DOID:5263
 * ovary mixed epithelial carcinoma
 * class of disease
 * ovarian carcinoma
 * Human disease
 * DOID:6898 DOID:6899
 * ovary neuroendocrine neoplasm
 * class of disease
 * ovarian cancer neuroendocrine tumor
 * Human disease
 * DOID:3002
 * ovary papillary carcinoma
 * class of disease
 * ovarian papillary neoplasm ovarian carcinoma
 * Human disease
 * DOID:6408
 * ovary rhabdomyosarcoma
 * class of disease
 * ovary sarcoma rhabdomyosarcoma
 * Human disease
 * DOID:4059
 * ovary sarcoma
 * class of disease
 * ovarian cancer sarcoma
 * human disease
 * DOID:2146
 * ovary serous adenocarcinoma
 * class of disease
 * ovary adenocarcinoma ovarian serous carcinoma
 * ovary adenocarcinoma that derives from the lining of a cavity that produces a serum-like fluid (a serous cavity)
 * DOID:5744
 * Serous adenocarcinoma of the ovary
 * overhydrated hereditary stomatocytosis
 * class of disease
 * macrocytic anemia autosomal dominant disease hereditary stomatocytosis
 * human disease
 * DOID:0111562
 * overnutrition
 * class of disease
 * nutrition disorder malnutrition
 * form of malnutrition in which the intake of nutrients is oversupplied
 * DOID:654
 * C18.654.726
 * ovine and caprine brucellosis
 * class of disease
 * brucellosis
 * A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.
 * DOID:14456
 * oxirane allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger oxirane
 * DOID:0040082
 * oxyphilic adenoma
 * class of disease
 * endocrine organ benign neoplasm oncocytic neoplasm benign epithelial neoplasm disease
 * Human disease
 * DOID:5389
 * C04.557.470.035.140
 * Oncocytoma
 * Parotid gland oncocytoma - very high mag.jpg
 * oxyphilic endometrial endometrioid adenocarcinoma
 * class of disease
 * endometrial adenocarcinoma
 * Human disease
 * DOID:6865
 * pain agnosia
 * class of disease
 * agnosia absence of pain sensation
 * agnosia that is a loss of the ability to perceive and process pain
 * DOID:0060145
 * pain disorder
 * class of disease
 * somatoform disorder disease pain
 * somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.
 * DOID:0060164
 * palindromic rheumatism
 * class of disease
 * syndrome arthritis
 * human disease
 * DOID:1166
 * palladium allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis metal allergy
 * allergic contact dermatitis that has allergic trigger palladium
 * DOID:0040055
 * palmoplantar keratosis
 * class of disease
 * keratosis foot diseases epidermal disease disease
 * keratosis characterized by abnormal thickening of the palms and the soles
 * DOID:3390
 * C16.320.850.475 C17.800.428.435 C17.800.827.475
 * Palmoplantar keratodermas
 * pancreas disease
 * class of disease
 * endocrine system disease
 * endocrine system disease that is located in the pancreas
 * DOID:26
 * C06.689
 * Diseases and disorders of pancreas
 * pancreas lymphoma
 * class of disease
 * pancreatic cancer lymphoma
 * human disease
 * DOID:1792
 * pancreas sarcoma
 * class of disease
 * pancreatic cancer sarcoma
 * pancreatic cancer that is located in the pancreas and that arises from transformed cells of mesenchymal origin
 * DOID:1796
 * pancreatic ACTH hormone producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:7697
 * pancreatic acinar cell adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma Acinar cell carcinoma of the pancreas acinar adenocarcinoma
 * pancreatic adenocarcinoma that has material basis in cells with morphological resemblance to acinar cells and is associated with increased serum lipase
 * DOID:5742
 * pancreatic adenocarcinoma
 * class of disease
 * pancreatic carcinoma adenocarcinoma
 * pancreatic carcinoma that derives from epithelial cells of glandular origin
 * DOID:4074
 * Adenocarcinomas of the pancreas
 * [[File:Metastatic pancreatic adenocarcinoma with lepidic growth pattern Case 280 (9840005374).jpg|center|64px]]
 * pancreatic cancer
 * class of disease
 * endocrine gland cancer pancreas disease pancreatic neoplasm gastrointestinal system cancer disease
 * endocrine gland cancer located in the pancreas
 * DOID:1793
 * Pancreatic cancer
 * MBq cystic-carcinoma-pancreas.jpg
 * pancreatic carcinoma
 * class of disease
 * pancreatic cancer carcinoma gastrointestinal carcinoma
 * pancreas cancer that derives from epithelial cells located in the pancreas
 * DOID:4905
 * pancreatic cholera
 * class of disease
 * endocrine pancreas disease
 * Human disease
 * DOID:6977
 * pancreatic colloid cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma mucinous cystadenocarcinoma
 * Human disease
 * DOID:7234
 * pancreatic cystadenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma cystadenocarcinoma
 * Human disease
 * DOID:4073
 * pancreatic cystadenoma
 * class of disease
 * benign neoplasm of exocrine pancreas endocrine organ benign neoplasm benign neoplasm of pancreas gastrointestinal system benign neoplasm pancreas disease
 * human disease
 * DOID:3918
 * pancreatic delta cell neoplasm
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:4433
 * pancreatic ductal adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * pancreatic adenocarcinoma that derives from pancreatic duct cells
 * DOID:3498
 * pancreatic ductal carcinoma
 * class of disease
 * pancreatic cancer ductal carcinoma pancreatic carcinoma
 * most common cancer of the pancreas
 * DOID:3587
 * C04.557.470.200.025.232.750 C04.557.470.615.132.750 C04.588.274.761.750 C04.588.322.475.750 C06.301.761.750 C06.689.667.625 C19.344.421.750
 * pancreatic foamy gland adenocarcinoma
 * class of disease
 * pancreatic adenocarcinoma
 * Human disease
 * DOID:7577
 * pancreatic gastrinoma
 * class of disease
 * islet cell tumor functional pancreatic neuroendocrine tumor
 * Human disease
 * DOID:5580
 * pancreatic intraductal papillary-colloid carcinoma
 * class of disease
 * pancreatic adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7574
 * pancreatic intraductal papillary-mucinous adenoma
 * class of disease
 * pancreatic intraductal papillary-mucinous neoplasm adenoma of pancreas gastrointestinal system benign neoplasm adenoma
 * Human disease
 * DOID:7851
 * pancreatic intraductal papillary-mucinous neoplasm
 * class of disease
 * cancer of exocrine pancreas
 * Human disease
 * DOID:7575
 * pancreatic invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma
 * Human disease
 * DOID:8150
 * pancreatic invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * Human disease
 * DOID:7236
 * pancreatic mucinous cystadenoma
 * class of disease
 * mucinous cystadenoma pancreatic cystadenoma
 * human disease
 * DOID:7235
 * pancreatic mucinous ductal ectasia
 * class of disease
 * pancreas disease
 * Human disease
 * DOID:13313
 * pancreatic non-functioning delta cell tumor
 * class of disease
 * pancreatic delta cell neoplasm non-functioning pancreatic endocrine tumor
 * Human disease
 * DOID:7840
 * pancreatic non-invasive intraductal papillary-mucinous carcinoma
 * class of disease
 * pancreatic intraductal papillary-colloid carcinoma pancreatic intraductal papillary-mucinous neoplasm
 * Human disease
 * DOID:7685
 * pancreatic non-invasive mucinous cystadenocarcinoma
 * class of disease
 * pancreatic colloid cystadenocarcinoma
 * human disease
 * DOID:7237
 * pancreatic serous cystadenocarcinoma
 * class of disease
 * pancreatic cystadenocarcinoma serous cystadenocarcinoma pancreatic serous cystic neoplasm
 * Human disease
 * DOID:5751
 * pancreatic serous cystadenoma
 * class of disease
 * serous cystadenoma pancreatic cystadenoma disease
 * human disease
 * DOID:3917
 * Serous cystadenoma pancreas
 * pancreatic serous cystic neoplasm
 * class of disease
 * pancreatic exocrine neoplasm Serous tumour cystic lesions of the pancreas cancer of exocrine pancreas
 * Human disease
 * DOID:3919
 * Serous cystic neoplasms of the pancreas
 * pancreatic signet ring cell adenocarcinoma
 * class of disease
 * pancreatic ductal adenocarcinoma signet ring cell adenocarcinoma
 * Human disease
 * DOID:3497
 * pancreatic solid pseudopapillary carcinoma
 * class of disease
 * pancreatic carcinoma
 * pancreatic carcinoma that is characterized by its papillary architecture
 * DOID:6827
 * pancreatic somatostatinoma
 * class of disease
 * islet cell tumor pancreatic delta cell neoplasm somatostatinoma
 * Human disease
 * DOID:4432
 * pancreatic squamous cell carcinoma
 * class of disease
 * pancreatic cancer squamous cell carcinoma
 * squamous cell carcinoma located in the pancreas
 * DOID:0080323
 * pancreatic steatorrhea
 * class of disease
 * pancreas disease steatorrhea
 * Human disease
 * DOID:10610
 * pancreatic vasoactive intestinal peptide producing tumor
 * class of disease
 * islet cell tumor
 * Human disease
 * DOID:5741
 * pancreatoblastoma
 * class of disease
 * pancreatic carcinoma rare epithelial tumor of pancreas disease
 * Human disease
 * DOID:6823
 * pancytopenia
 * class of disease
 * anemia cytopenia disease
 * medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets
 * DOID:12450
 * C15.378.243.875
 * panhypopituitarism, X-linked
 * class of disease
 * panhypopituitarism X-linked disease
 * human disease
 * DOID:0111779
 * panic disorder
 * class of disease
 * anxiety disorder disease
 * anxiety disorder characterized by reoccurring unexpected panic attacks
 * DOID:594
 * F03.080.700
 * Panic disorder
 * Panic attack.jpg
 * panniculitis
 * class of disease
 * fibromyalgia connective tissue disease skin disease disease
 * Inflammation of the subcutaneous adipose tissue
 * DOID:1526
 * C17.300.710 C17.800.566
 * Panniculitis
 * An introduction to dermatology (1905) erythema induratum 2.jpg
 * panuveitis
 * class of disease
 * uveitis
 * Human disease
 * DOID:12030
 * C11.941.879.780
 * papillary adenocarcinoma
 * class of disease
 * adenocarcinoma
 * adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue
 * DOID:3112
 * C04.557.470.200.025.085
 * papillary adenofibroma
 * class of disease
 * adenofibroma
 * biphasic polypoid neoplasm characterized by the presence of papillary projections that are lined by epithelial cells and fibrotic stroma
 * DOID:5479
 * papillary adenoma
 * class of disease
 * glandular cell epithelial neoplasm adenoma
 * Human disease
 * DOID:3172
 * papillary carcinoma
 * class of disease
 * carcinoma
 * carcinoma derived from epithelial cells with finger-like projections
 * DOID:3113
 * C04.557.470.200.360 C04.557.470.700.360
 * papillary conjunctivitis
 * class of disease
 * conjunctivitis
 * Human disease
 * DOID:2458
 * papillary craniopharyngioma
 * class of disease
 * craniopharyngioma
 * Human disease
 * DOID:3847
 * papillary cystadenocarcinoma
 * class of disease
 * cystadenocarcinoma papillary cystic tumor
 * cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with cysts and papillary endophytic projections
 * DOID:3110
 * C04.557.470.200.025.480.230 C04.557.470.590.480.230
 * papillary eccrine adenoma
 * class of disease
 * eccrine sweat gland neoplasm papillary adenoma
 * Human disease
 * DOID:5446
 * papillary ependymoma
 * class of disease
 * benign ependymoma
 * human disease
 * DOID:5505
 * papillary extrahepatic bile duct adenocarcinoma
 * class of disease
 * extrahepatic bile duct adenocarcinoma
 * Human disease
 * DOID:6931
 * papillary follicular thyroid adenocarcinoma
 * class of disease
 * papillary thyroid cancer
 * Human disease
 * DOID:3968
 * C04.557.470.200.025.060.225 C04.557.470.200.025.085.225
 * papillary hidradenoma
 * class of disease
 * hidradenoma
 * Human disease
 * DOID:5439
 * Papillary hidradenoma
 * Papillary hidradenoma - very high mag.jpg
 * papillary meningioma of the cerebellum
 * class of disease
 * cerebellum cancer rhabdoid meningioma papillary meningioma brain meningioma
 * Human disease
 * DOID:5057
 * papillary pattern testicular yolk sac tumor
 * class of disease
 * testicular yolk sac tumor
 * Human disease
 * DOID:8193
 * papillary renal cell carcinomas
 * class of disease
 * renal cell carcinoma
 * renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors
 * DOID:4465
 * [[File:Histopathology of papillary renal cell carcinoma type 1, grade 2, with variable density.jpg|center|64px]]
 * papillary serous adenocarcinoma
 * class of disease
 * papillary adenocarcinoma
 * papillary adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures with psammoma bodies
 * DOID:2632
 * papillary squamous carcinoma
 * class of disease
 * squamous cell carcinoma papillary carcinoma
 * Human disease
 * DOID:4385
 * papillary thymic adenocarcinoma
 * class of disease
 * thymus adenocarcinoma
 * Human disease
 * DOID:5595
 * papillary thyroid cancer
 * class of disease
 * thyroid carcinoma papillary carcinoma differentiated thyroid carcinoma
 * thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer
 * DOID:3969
 * C04.557.470.200.025.085.612 C04.588.322.894.400 C04.588.443.915.400 C19.344.894.400 C19.874.788.400
 * Thyroid papillary carcinoma
 * papillary transitional carcinoma
 * class of disease
 * transitional cell carcinoma
 * transitional cell carcinoma that has several papillary fronds with central fibrovascular core lined by transitional type epithelium
 * DOID:4012
 * Urothelial papillary carcinoma
 * papillary urothelial neoplasm of low malignant potential
 * class of disease
 * bladder papillary transitional cell neoplasm urinary tract non-invasive transitional cell neoplasm papillary urothelial lesion
 * human disease
 * DOID:6239
 * papilledema
 * class of disease
 * optic nerve disease disease
 * Human disease
 * DOID:146
 * C10.292.700.900 C11.640.710
 * Papilledema
 * Papilledema.jpg
 * papilloma
 * class of disease
 * benign neoplasms by histologic type papillary tumor disease
 * cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue
 * DOID:2615
 * C04.557.470.700.600
 * Papillomas
 * parachordoma
 * class of disease
 * mesenchymal cell neoplasm
 * Human disease
 * DOID:2647
 * paralytic ileus
 * class of disease
 * bowel obstruction ileus
 * Human disease
 * DOID:8442
 * Paralytic ileus
 * paralytic lagophthalmos
 * class of disease
 * lagophthalmos
 * Human disease
 * DOID:12958
 * paralytic poliomyelitis
 * class of disease
 * poliomyelitis central nervous system disease
 * Human disease
 * DOID:0050515
 * paralytic squint
 * class of disease
 * strabismus cranial nerve palsy
 * Human disease
 * DOID:10863
 * parameningeal embryonal rhabdomyosarcoma
 * class of disease
 * embryonal rhabdomyosarcoma
 * embryonal rhabdomyosarcoma located in the parameningeal region
 * DOID:0060338
 * parametritis
 * class of disease
 * pelvic inflammatory diseases inflammatory disease uterine disease
 * Human disease
 * DOID:1260
 * C13.351.500.056.750.750
 * parametrium malignant neoplasm
 * class of disease
 * uterine adnexa cancer broad ligament malignant neoplasm
 * Human disease
 * DOID:11746
 * paramyotonia congenita of Von Eulenburg
 * class of disease
 * neuromuscular disease autosomal dominant disease paramyotonia congenita
 * human disease
 * DOID:0111538
 * paranasal sinus disease
 * class of disease
 * nose disease
 * respiratory disease
 * DOID:1352
 * C08.460.692 C09.603.692
 * paranasal sinus lymphoma
 * class of disease
 * paranasal sinus cancer lymphoma
 * human disease
 * DOID:1355
 * paranasal sinus neoplasm
 * class of disease
 * respiratory tract neoplasm paranasal sinus disease respiratory system benign neoplasm
 * human disease
 * DOID:1350
 * C04.588.443.665.650.693 C08.460.669.693 C08.460.692.503 C08.785.600.693 C09.603.669.693 C09.603.692.503 C09.647.685.693
 * Neoplasms of paranasal sinuses
 * paranasal sinus sarcoma
 * class of disease
 * paranasal sinus cancer sarcoma
 * sarcoma and malignant tumor of nasal sinuses that is located in the paranasal sinus
 * DOID:1362
 * paraneoplastic pemphigus
 * class of disease
 * pemphigus
 * human disease
 * DOID:0080852
 * paraneoplastic polyneuropathy
 * class of disease
 * inflammatory and toxic neuropathy peripheral neuropathy paraneoplastic neurologic syndrome
 * Human disease
 * DOID:8681
 * C04.588.614.550.700 C04.730.856.700 C10.574.781.850 C10.668.829.800.662
 * paranoid personality disorder
 * class of disease
 * personality disorder disease
 * mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others
 * DOID:10938
 * F03.675.600
 * Paranoid personality disorder
 * parapharyngeal meningioma
 * class of disease
 * meningioma
 * Human disease
 * DOID:8216
 * paraphilia
 * class of disease
 * psychosexual disorder sexual and gender disorder disease
 * experience of intense sexual arousal to atypical objects, situations, or individuals
 * DOID:0060044
 * F03.657
 * Paraphilias
 * Martin van Maele - La Comtesse au fouet 01.jpg
 * paraphimosis
 * class of disease
 * phimosis disease
 * medical condition in which the foreskin of a penis becomes trapped behind the glans penis
 * DOID:5334
 * C12.294.494.684.587
 * Paraphimosis
 * Paraphimosis.jpg
 * paraplegia
 * class of disease symptom or sign
 * central nervous system disease paralysis disease
 * impairment in motor or sensory function of the lower extremities
 * DOID:607
 * C10.597.622.669 C23.888.592.636.637
 * Paraplegia
 * parapsoriasis
 * class of disease
 * psoriasis disease
 * Human disease
 * DOID:9088
 * C17.800.859.575
 * parasagittal meningioma
 * class of disease
 * cerebral convexity meningioma
 * Human disease
 * DOID:6869
 * parasitic Ichthyosporea infectious disease
 * class of disease
 * parasitic infectious diseases
 * parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals
 * DOID:0050291
 * C03.600
 * parasitic conjunctivitis
 * class of disease
 * chronic conjunctivitis parasitic eye infection
 * Human disease
 * DOID:13341
 * parasitic eyelid infestation
 * class of disease
 * blepharitis parasitic eye infection
 * Human disease
 * DOID:13823
 * parasitic protozoa infectious disease
 * class of disease
 * parasitic infectious diseases disease
 * parasitic disease caused by a protozoan
 * DOID:2789
 * C01.610.752
 * paratesticular lipoma
 * class of disease
 * reproductive organ benign neoplasm lipoma
 * Human disease
 * DOID:10207
 * parathyroid adenoma
 * class of disease
 * parathyroid neoplasm benign parathyroid gland neoplasm benign neoplasms by histologic type adenoma disease
 * Human disease
 * DOID:7608
 * Parathyroid adenoma
 * parathyroid gland disease
 * class of disease
 * endocrine system disease
 * endocrine disease
 * DOID:11201
 * C19.642
 * parathyroid oncocytic adenoma
 * class of disease
 * parathyroid adenoma oxyphilic adenoma
 * Human disease
 * DOID:7611
 * parathyroid transitional clear cell adenoma
 * class of disease
 * parathyroid adenoma
 * Human disease
 * DOID:7609
 * paraurethral gland cancer
 * class of disease
 * female reproductive organ cancer paraurethral gland neoplasm
 * Human disease
 * DOID:14059
 * paraurethral gland neoplasm
 * class of disease
 * urethral benign neoplasm
 * Human disease
 * DOID:2139
 * parenchymatous neurosyphilis
 * class of disease
 * tertiary neurosyphilis
 * Human disease
 * DOID:0050490
 * parietal lobe ependymoma
 * class of disease
 * parietal lobe malignant neoplasm ependymoma
 * parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain
 * DOID:0050903
 * paronychia
 * class of disease
 * nail disease disease
 * bacterial or fungal nail infection of the hand or foot
 * DOID:13117
 * C01.539.800.460 C17.800.529.639 C17.800.838.486
 * Paronychia (disease)
 * Paronychia.jpg
 * parotid disease
 * class of disease
 * salivary gland disease
 * Human disease
 * DOID:10302
 * C07.465.815.470
 * Diseases and disorders of parotid glands
 * parotitis
 * class of disease
 * parotid disease inflammatory disease sialadenitis disease
 * parotid disease characterized by the inflammation of one or both parotid glands
 * DOID:10301
 * C07.465.815.470.800 C07.465.815.793.500
 * parovarian cyst
 * class of disease
 * female reproductive system disease embryonic cyst of fallopian tube
 * Human disease
 * DOID:4333
 * C04.182.668 C23.300.306.500
 * paroxysmal nonkinesigenic dyskinesia 2
 * class of disease
 * Paroxysmal dyskinesia dystonia genetic disease
 * human disease
 * DOID:0090047
 * pars planitis
 * class of disease
 * intermediate uveitis chorioretinitis ciliary body disease rare genetic eye disease disease
 * Human disease
 * DOID:12731
 * C11.941.160.478.700 C11.941.879.780.900.300.659 C11.941.879.900.500
 * parthenolide allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger parthenolide
 * DOID:0040072
 * partial androgen insensitivity syndrome
 * class of disease
 * X-linked recessive disease androgen insensitivity syndrome
 * medical condition
 * DOID:0080776
 * partial arterial retinal occlusion
 * class of disease
 * retinal artery occlusion
 * Human disease
 * DOID:14522
 * partial circumpapillary choroid dystrophy
 * class of disease
 * hereditary choroidal atrophy
 * human disease
 * DOID:9811
 * partial lipodystrophy
 * class of disease
 * lipodystrophy
 * lipodystrophy that is characterized by partial loss of adipose tissue
 * DOID:0080299
 * partial motor epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3327
 * C10.228.140.490.360.272
 * partial optic atrophy
 * class of disease
 * optic atrophy
 * human disease
 * DOID:10631
 * partial pancreatic agenesis
 * class of disease
 * pancreas disease agenesis pancreatic agenesis
 * pancreas disease that is characterized by the failure of the pancreas to develop prior to birth
 * DOID:0050877
 * partial retinal vein occlusion
 * class of disease
 * retinal vein occlusion
 * Human disease
 * DOID:1726
 * partial sensory epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3330
 * C10.228.140.490.360.275
 * partial third-nerve palsy
 * class of disease
 * paralytic squint oculomotor nerve paralysis
 * Human disease
 * DOID:10864
 * patellar tendinitis
 * class of disease
 * tendinitis knee disorder knee extensor tendonitis
 * Human disease
 * DOID:10471
 * Patellar tendinitis
 * patent blue V allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger patent blue V
 * DOID:0040080
 * paternal uniparental disomy of chromosome 14
 * class of disease
 * uniparental disomy of paternal origin uniparental disomy 14 syndrome
 * human disease
 * DOID:0111712
 * pathologic nystagmus
 * class of disease
 * nystagmus ocular motility disease abnormal eye movements
 * Human disease
 * DOID:9650
 * C10.292.562.675 C11.590.400
 * patterned macular dystrophy 1
 * class of disease
 * patterned macular dystrophy
 * human disease
 * DOID:0060866
 * patulous eustachian tube
 * class of disease physiological condition
 * eustachian tube disease
 * eustachian tube disorder
 * DOID:12358
 * peach allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus persica plant fruit food product.
 * DOID:0060510
 * peanut allergy
 * class of disease
 * tree nut allergy legume allergy vegetable allergy
 * type of food allergy caused by peanuts
 * DOID:4378
 * C20.543.480.370.572.750
 * Nut warning 1.jpg
 * pediatric CNS choriocarcinoma
 * class of disease
 * malignant childhood germ cell neoplasm central nervous system choriocarcinoma rare childhood malignant neoplasm choriocarcinoma
 * Human disease
 * DOID:6639
 * pediatric CNS embryonal cell carcinoma
 * class of disease
 * central nervous system childhood germ cell tumor central nervous system embryonal carcinoma rare childhood malignant neoplasm malignant childhood germ cell neoplasm brain cancer
 * Human disease
 * DOID:7231
 * pediatric angiosarcoma
 * class of disease
 * angiosarcoma rare childhood malignant neoplasm
 * angiosarcoma that affects children
 * DOID:4505
 * pediatric cerebral ependymoblastoma
 * class of disease
 * ependymoblastoma
 * Human disease
 * DOID:7841
 * pediatric ependymoma
 * class of disease
 * ependymoma childhood cancer ependymal tumor childhood neoplasm
 * human disease
 * DOID:5509
 * pediatric epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7095
 * pediatric fibrosarcoma
 * class of disease
 * fibrosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3520
 * pediatric germ cell tumor
 * class of disease
 * germ cell tumor childhood neoplasm
 * Human disease
 * DOID:6053
 * pediatric hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma childhood cancer of liver
 * Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age
 * DOID:0070322
 * pediatric infratentorial ependymoblastoma
 * class of disease
 * childhood infratentorial neoplasm ependymoblastoma infratentorial cancer childhood central nervous system primitive neuroectodermal neoplasm rare childhood malignant neoplasm
 * Human disease
 * DOID:7522
 * pediatric infratentorial ependymoma
 * class of disease
 * infratentorial cancer pediatric ependymoma brain ependymoma childhood infratentorial neoplasm childhood cancer
 * Human disease
 * DOID:7501
 * pediatric leptomeningeal melanoma
 * class of disease
 * meningeal melanoma
 * Human disease
 * DOID:6089
 * pediatric liposarcoma
 * class of disease
 * liposarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5695
 * pediatric low-grade glioma
 * class of disease
 * low grade glioma
 * human disease
 * DOID:0080830
 * pediatric lymphoma
 * class of disease
 * lymphoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5823
 * pediatric meningioma
 * class of disease
 * meningioma pediatric central nervous system tumor
 * Human disease
 * DOID:4593
 * pediatric mesenchymal chondrosarcoma
 * class of disease
 * mesenchymal chondrosarcoma childhood cancer
 * Human disease
 * DOID:4546
 * pediatric myxoid chondrosarcoma
 * class of disease
 * myxoid chondrosarcoma childhood cancer
 * Human disease
 * DOID:6494
 * pediatric osteosarcoma
 * class of disease
 * osteosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3361
 * pediatric ovarian dysgerminoma
 * class of disease
 * pediatric ovarian germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm dysgerminoma of ovary
 * dysgerminoma of ovary that occurs in children
 * DOID:7340
 * pediatric ovarian germ cell tumor
 * class of disease
 * ovarian germ cell neoplasm pediatric germ cell tumor
 * Human disease
 * DOID:6084
 * pediatric supratentorial ependymoma
 * class of disease
 * supratentorial cancer pediatric ependymoma brain ependymoma
 * Human disease
 * DOID:7502
 * pediatric testicular germ cell tumor
 * class of disease
 * testicular germ cell tumor pediatric germ cell tumor
 * Human disease
 * DOID:6082
 * peliosis hepatis
 * class of disease
 * hepatic vascular disease
 * Human disease
 * DOID:914
 * C06.552.802
 * Peliosis hepatis
 * pellagra
 * class of disease
 * nutritional deficiency disease other acquired skin disease skin disease disease
 * Human disease
 * DOID:8457
 * C18.654.521.500.133.699.529
 * Pellagra
 * Pellagra NIH.jpg
 * pelvic inflammatory diseases
 * class of disease
 * female reproductive system disease adnexal disease infectious disease disease
 * infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis
 * DOID:1003
 * C01.635.500 C12.050.351.500.056.750 C12.100.250.056.750
 * Pelvic inflammatory disease
 * Blausen 0732 PID-Sites.png
 * pelvic lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3927
 * pelvic muscle wasting
 * class of disease
 * pelvic organ prolapse pelvic floor dysfunction
 * Human disease
 * DOID:11629
 * pelvic organ prolapse
 * class of disease
 * female reproductive system disease prolapse
 * pelvic organs protruding from the opening of the vagina
 * DOID:1284
 * C23.300.842.624
 * Female genital prolapse
 * Hippocrates treatment for prolapse.png
 * pelvic varices
 * class of disease
 * varicose veins
 * Human disease
 * DOID:9742
 * pemphigoid
 * class of disease
 * autoimmune skin disease bullous skin disease
 * human disease
 * DOID:0080841
 * penicillin drug reaction
 * class of disease
 * adverse drug reaction beta-lactam allergy Side effects of penicillin
 * beta-lactam allergy triggered by penicillin
 * DOID:0060520
 * penicilliosis
 * class of disease
 * opportunistic mycosis disease
 * Human disease
 * DOID:0050288
 * penile cancer
 * class of disease
 * penile neoplasm male reproductive organ cancer penile disease disease
 * cancer of the penis
 * DOID:11615
 * Penile cancer
 * Penile cancer 2.jpg
 * penile disease
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:1529
 * C12.294.494
 * penile neoplasm
 * class of disease
 * male reproductive system neoplasm penile disease male reproductive organ benign neoplasm
 * human disease
 * DOID:11624
 * C04.588.945.440.715 C12.294.260.500 C12.294.494.591 C12.758.409.500
 * Penile neoplasms
 * penile urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8223
 * penis Paget's disease
 * class of disease
 * penis carcinoma extramammary Paget's disease adenocarcinoma of penis genetic urogenital tumor
 * Human disease
 * DOID:3448
 * Penile Paget's disease
 * penis basal cell carcinoma
 * class of disease
 * penis carcinoma basal-cell carcinoma rare skin disease
 * human disease
 * DOID:4277
 * penis basaloid carcinoma
 * class of disease
 * penis squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7047
 * penis carcinoma
 * class of disease
 * penile cancer carcinoma
 * penile cancer that is located in the skin or tissues of the penis
 * DOID:3449
 * penis carcinoma in situ
 * class of disease
 * in situ carcinoma penile disease penis squamous cell carcinoma carcinoma in situ of male genital organs
 * Human disease
 * DOID:8872
 * penis mixed squamous cell carcinoma
 * class of disease
 * penis squamous cell carcinoma
 * Human disease
 * DOID:8009
 * penis non-invasive verrucous carcinoma
 * class of disease
 * penis verrucous carcinoma penis carcinoma in situ cervical verrucous carcinoma
 * Human disease
 * DOID:5907
 * penis papillary carcinoma
 * class of disease
 * penis squamous cell carcinoma papillary squamous carcinoma
 * Human disease
 * DOID:8013
 * penis sarcoma
 * class of disease
 * penile cancer sarcoma
 * sarcoma and malignant neoplasm of penis that is located in the penis
 * DOID:11838
 * penis squamous cell carcinoma
 * class of disease
 * penis carcinoma squamous cell carcinoma
 * penis carcinoma that has material basis in squamous cells
 * DOID:5518
 * Squamous-cell carcinoma of the penis
 * penis verrucous carcinoma
 * class of disease
 * penis squamous cell carcinoma verrucous carcinoma penis papillary carcinoma
 * Human disease
 * DOID:5908
 * peptic esophagitis
 * class of disease
 * peptic ulcer disease esophagitis gastroesophageal reflux disease
 * human disease
 * DOID:13976
 * C06.405.117.620.420 C06.405.205.663.420 C06.405.469.275.800.523 C06.405.748.586.524
 * peptic ulcer disease
 * class of disease
 * gastrointestinal system disease duodenal disease disease
 * ulcer of an area of the gastrointestinal tract
 * DOID:750
 * C06.405.469.275.800 C06.405.748.586
 * Peptic ulcers
 * Benign gastric ulcer 1.jpg
 * perforated corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10445
 * perforated ulcer
 * class of disease
 * peptic ulcer disease gastric perforation
 * medical condition of the gastrointestinal tract wall
 * DOID:752
 * C06.405.469.275.800.698 C06.405.748.586.698
 * DU 2.jpg
 * perforation of bile duct
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:13409
 * periampullary adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma
 * Human disease
 * DOID:8110
 * periampullary adenoma
 * class of disease
 * ampulla of Vater neoplasm adenoma
 * Human disease
 * DOID:0050849
 * perianal gland tumor
 * class of disease
 * cancer in dogs anus neoplasm
 * dog disease
 * DOID:4550
 * C04.588.083 C04.588.274.476.411.307.790.040.040 C06.301.371.411.307.790.040.040 C06.405.249.411.307.790.040.040 C06.405.469.491.307.790.040.040 C06.405.469.860.101.163.083 C06.405.469.860.180.500.040.040 C22.073
 * perianal hematoma
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9745
 * Perianal hematoma
 * perianal skin Paget's disease
 * class of disease
 * anal margin carcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:7708
 * periapical abscess
 * class of disease
 * periapical periodontitis dental abscess
 * localized collection of pus associated with a tooth
 * DOID:2562
 * C01.539.830.025.650 C07.320.830.700.700 C07.465.714.306.700.700 C07.465.714.533.487.700
 * periapical periodontitis
 * class of disease
 * inflammation periodontitis dental pulp disease periapical disease tooth pathology
 * Human disease
 * DOID:823
 * C07.320.830.700 C07.465.714.306.700 C07.465.714.533.487
 * pericardial effusion
 * class of disease symptom or sign
 * pericardium disease cardiovascular system symptom disease
 * pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
 * DOID:118
 * C14.280.695
 * Pericardial effusion
 * pericardial mesothelioma
 * class of disease
 * pericardium cancer mesothelioma
 * Human disease
 * DOID:6201
 * pericarditis
 * class of disease
 * pericardium disease inflammation inflammatory disease heart disease disease
 * pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
 * DOID:1787
 * C14.280.720
 * Pericarditis
 * Pericarditis10.JPG
 * pericardium cancer
 * class of disease
 * heart cancer neoplasm of pericardium pericardium disease
 * Human disease
 * DOID:116
 * pericardium leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of pericardium pericardium disease cardiovascular organ benign neoplasm
 * Human disease
 * DOID:5137
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * class of disease
 * parasitic infectious diseases
 * parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals
 * DOID:0050291
 * C03.600
 * parasitic conjunctivitis
 * class of disease
 * chronic conjunctivitis parasitic eye infection
 * Human disease
 * DOID:13341
 * parasitic eyelid infestation
 * class of disease
 * blepharitis parasitic eye infection
 * Human disease
 * DOID:13823
 * parasitic protozoa infectious disease
 * class of disease
 * parasitic infectious diseases disease
 * parasitic disease caused by a protozoan
 * DOID:2789
 * C01.610.752
 * paratesticular lipoma
 * class of disease
 * reproductive organ benign neoplasm lipoma
 * Human disease
 * DOID:10207
 * parathyroid adenoma
 * class of disease
 * parathyroid neoplasm benign parathyroid gland neoplasm benign neoplasms by histologic type adenoma disease
 * Human disease
 * DOID:7608
 * Parathyroid adenoma
 * parathyroid gland disease
 * class of disease
 * endocrine system disease
 * endocrine disease
 * DOID:11201
 * C19.642
 * parathyroid oncocytic adenoma
 * class of disease
 * parathyroid adenoma oxyphilic adenoma
 * Human disease
 * DOID:7611
 * parathyroid transitional clear cell adenoma
 * class of disease
 * parathyroid adenoma
 * Human disease
 * DOID:7609
 * paraurethral gland cancer
 * class of disease
 * female reproductive organ cancer paraurethral gland neoplasm
 * Human disease
 * DOID:14059
 * paraurethral gland neoplasm
 * class of disease
 * urethral benign neoplasm
 * Human disease
 * DOID:2139
 * parenchymatous neurosyphilis
 * class of disease
 * tertiary neurosyphilis
 * Human disease
 * DOID:0050490
 * parietal lobe ependymoma
 * class of disease
 * parietal lobe malignant neoplasm ependymoma
 * parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain
 * DOID:0050903
 * paronychia
 * class of disease
 * nail disease disease
 * bacterial or fungal nail infection of the hand or foot
 * DOID:13117
 * C01.539.800.460 C17.800.529.639 C17.800.838.486
 * Paronychia (disease)
 * Paronychia.jpg
 * parotid disease
 * class of disease
 * salivary gland disease
 * Human disease
 * DOID:10302
 * C07.465.815.470
 * Diseases and disorders of parotid glands
 * parotitis
 * class of disease
 * parotid disease inflammatory disease sialadenitis disease
 * parotid disease characterized by the inflammation of one or both parotid glands
 * DOID:10301
 * C07.465.815.470.800 C07.465.815.793.500
 * parovarian cyst
 * class of disease
 * female reproductive system disease embryonic cyst of fallopian tube
 * Human disease
 * DOID:4333
 * C04.182.668 C23.300.306.500
 * paroxysmal nonkinesigenic dyskinesia 2
 * class of disease
 * Paroxysmal dyskinesia dystonia genetic disease
 * human disease
 * DOID:0090047
 * pars planitis
 * class of disease
 * intermediate uveitis chorioretinitis ciliary body disease rare genetic eye disease disease
 * Human disease
 * DOID:12731
 * C11.941.160.478.700 C11.941.879.780.900.300.659 C11.941.879.900.500
 * parthenolide allergic contact dermatitis
 * class of disease
 * allergic contact dermatitis
 * allergic contact dermatitis that has allergic trigger parthenolide
 * DOID:0040072
 * partial androgen insensitivity syndrome
 * class of disease
 * X-linked recessive disease androgen insensitivity syndrome
 * medical condition
 * DOID:0080776
 * partial arterial retinal occlusion
 * class of disease
 * retinal artery occlusion
 * Human disease
 * DOID:14522
 * partial circumpapillary choroid dystrophy
 * class of disease
 * hereditary choroidal atrophy
 * human disease
 * DOID:9811
 * partial lipodystrophy
 * class of disease
 * lipodystrophy
 * lipodystrophy that is characterized by partial loss of adipose tissue
 * DOID:0080299
 * partial motor epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3327
 * C10.228.140.490.360.272
 * partial optic atrophy
 * class of disease
 * optic atrophy
 * human disease
 * DOID:10631
 * partial pancreatic agenesis
 * class of disease
 * pancreas disease agenesis pancreatic agenesis
 * pancreas disease that is characterized by the failure of the pancreas to develop prior to birth
 * DOID:0050877
 * partial retinal vein occlusion
 * class of disease
 * retinal vein occlusion
 * Human disease
 * DOID:1726
 * partial sensory epilepsy
 * class of disease
 * focal epilepsy
 * Human disease
 * DOID:3330
 * C10.228.140.490.360.275
 * partial third-nerve palsy
 * class of disease
 * paralytic squint oculomotor nerve paralysis
 * Human disease
 * DOID:10864
 * patellar tendinitis
 * class of disease
 * tendinitis knee disorder knee extensor tendonitis
 * Human disease
 * DOID:10471
 * Patellar tendinitis
 * patent blue V allergy
 * class of disease
 * drug allergy
 * drug allergy that has allergic trigger patent blue V
 * DOID:0040080
 * paternal uniparental disomy of chromosome 14
 * class of disease
 * uniparental disomy of paternal origin uniparental disomy 14 syndrome
 * human disease
 * DOID:0111712
 * pathologic nystagmus
 * class of disease
 * nystagmus ocular motility disease abnormal eye movements
 * Human disease
 * DOID:9650
 * C10.292.562.675 C11.590.400
 * patterned macular dystrophy 1
 * class of disease
 * patterned macular dystrophy
 * human disease
 * DOID:0060866
 * patulous eustachian tube
 * class of disease physiological condition
 * eustachian tube disease
 * eustachian tube disorder
 * DOID:12358
 * peach allergy
 * class of disease
 * fruit allergy
 * fruit allergy triggered by Prunus persica plant fruit food product.
 * DOID:0060510
 * peanut allergy
 * class of disease
 * tree nut allergy legume allergy vegetable allergy
 * type of food allergy caused by peanuts
 * DOID:4378
 * C20.543.480.370.572.750
 * Nut warning 1.jpg
 * pediatric CNS choriocarcinoma
 * class of disease
 * malignant childhood germ cell neoplasm central nervous system choriocarcinoma rare childhood malignant neoplasm choriocarcinoma
 * Human disease
 * DOID:6639
 * pediatric CNS embryonal cell carcinoma
 * class of disease
 * central nervous system childhood germ cell tumor central nervous system embryonal carcinoma rare childhood malignant neoplasm malignant childhood germ cell neoplasm brain cancer
 * Human disease
 * DOID:7231
 * pediatric angiosarcoma
 * class of disease
 * angiosarcoma rare childhood malignant neoplasm
 * angiosarcoma that affects children
 * DOID:4505
 * pediatric cerebral ependymoblastoma
 * class of disease
 * ependymoblastoma
 * Human disease
 * DOID:7841
 * pediatric ependymoma
 * class of disease
 * ependymoma childhood cancer ependymal tumor childhood neoplasm
 * human disease
 * DOID:5509
 * pediatric epithelioid sarcoma
 * class of disease
 * epithelioid sarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:7095
 * pediatric fibrosarcoma
 * class of disease
 * fibrosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3520
 * pediatric germ cell tumor
 * class of disease
 * germ cell tumor childhood neoplasm
 * Human disease
 * DOID:6053
 * pediatric hepatocellular carcinoma
 * class of disease
 * hepatocellular carcinoma childhood cancer of liver
 * Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age
 * DOID:0070322
 * pediatric infratentorial ependymoblastoma
 * class of disease
 * childhood infratentorial neoplasm ependymoblastoma infratentorial cancer childhood central nervous system primitive neuroectodermal neoplasm rare childhood malignant neoplasm
 * Human disease
 * DOID:7522
 * pediatric infratentorial ependymoma
 * class of disease
 * infratentorial cancer pediatric ependymoma brain ependymoma childhood infratentorial neoplasm childhood cancer
 * Human disease
 * DOID:7501
 * pediatric leptomeningeal melanoma
 * class of disease
 * meningeal melanoma
 * Human disease
 * DOID:6089
 * pediatric liposarcoma
 * class of disease
 * liposarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5695
 * pediatric low-grade glioma
 * class of disease
 * low grade glioma
 * human disease
 * DOID:0080830
 * pediatric lymphoma
 * class of disease
 * lymphoma rare childhood malignant neoplasm
 * Human disease
 * DOID:5823
 * pediatric meningioma
 * class of disease
 * meningioma pediatric central nervous system tumor
 * Human disease
 * DOID:4593
 * pediatric mesenchymal chondrosarcoma
 * class of disease
 * mesenchymal chondrosarcoma childhood cancer
 * Human disease
 * DOID:4546
 * pediatric myxoid chondrosarcoma
 * class of disease
 * myxoid chondrosarcoma childhood cancer
 * Human disease
 * DOID:6494
 * pediatric osteosarcoma
 * class of disease
 * osteosarcoma rare childhood malignant neoplasm
 * Human disease
 * DOID:3361
 * pediatric ovarian dysgerminoma
 * class of disease
 * pediatric ovarian germ cell tumor rare childhood malignant neoplasm malignant childhood germ cell neoplasm dysgerminoma of ovary
 * dysgerminoma of ovary that occurs in children
 * DOID:7340
 * pediatric ovarian germ cell tumor
 * class of disease
 * ovarian germ cell neoplasm pediatric germ cell tumor
 * Human disease
 * DOID:6084
 * pediatric supratentorial ependymoma
 * class of disease
 * supratentorial cancer pediatric ependymoma brain ependymoma
 * Human disease
 * DOID:7502
 * pediatric testicular germ cell tumor
 * class of disease
 * testicular germ cell tumor pediatric germ cell tumor
 * Human disease
 * DOID:6082
 * peliosis hepatis
 * class of disease
 * hepatic vascular disease
 * Human disease
 * DOID:914
 * C06.552.802
 * Peliosis hepatis
 * pellagra
 * class of disease
 * nutritional deficiency disease other acquired skin disease skin disease disease
 * Human disease
 * DOID:8457
 * C18.654.521.500.133.699.529
 * Pellagra
 * Pellagra NIH.jpg
 * pelvic inflammatory diseases
 * class of disease
 * female reproductive system disease adnexal disease infectious disease disease
 * infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis
 * DOID:1003
 * C01.635.500 C12.050.351.500.056.750 C12.100.250.056.750
 * Pelvic inflammatory disease
 * Blausen 0732 PID-Sites.png
 * pelvic lipomatosis
 * class of disease
 * lipomatosis
 * Human disease
 * DOID:3927
 * pelvic muscle wasting
 * class of disease
 * pelvic organ prolapse pelvic floor dysfunction
 * Human disease
 * DOID:11629
 * pelvic organ prolapse
 * class of disease
 * female reproductive system disease prolapse
 * pelvic organs protruding from the opening of the vagina
 * DOID:1284
 * C23.300.842.624
 * Female genital prolapse
 * Hippocrates treatment for prolapse.png
 * pelvic varices
 * class of disease
 * varicose veins
 * Human disease
 * DOID:9742
 * pemphigoid
 * class of disease
 * autoimmune skin disease bullous skin disease
 * human disease
 * DOID:0080841
 * penicillin drug reaction
 * class of disease
 * adverse drug reaction beta-lactam allergy Side effects of penicillin
 * beta-lactam allergy triggered by penicillin
 * DOID:0060520
 * penicilliosis
 * class of disease
 * opportunistic mycosis disease
 * Human disease
 * DOID:0050288
 * penile cancer
 * class of disease
 * penile neoplasm male reproductive organ cancer penile disease disease
 * cancer of the penis
 * DOID:11615
 * Penile cancer
 * Penile cancer 2.jpg
 * penile disease
 * class of disease
 * male reproductive system disease
 * Human disease
 * DOID:1529
 * C12.294.494
 * penile neoplasm
 * class of disease
 * male reproductive system neoplasm penile disease male reproductive organ benign neoplasm
 * human disease
 * DOID:11624
 * C04.588.945.440.715 C12.294.260.500 C12.294.494.591 C12.758.409.500
 * Penile neoplasms
 * penile urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8223
 * penis Paget's disease
 * class of disease
 * penis carcinoma extramammary Paget's disease adenocarcinoma of penis genetic urogenital tumor
 * Human disease
 * DOID:3448
 * Penile Paget's disease
 * penis basal cell carcinoma
 * class of disease
 * penis carcinoma basal-cell carcinoma rare skin disease
 * human disease
 * DOID:4277
 * penis basaloid carcinoma
 * class of disease
 * penis squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7047
 * penis carcinoma
 * class of disease
 * penile cancer carcinoma
 * penile cancer that is located in the skin or tissues of the penis
 * DOID:3449
 * penis carcinoma in situ
 * class of disease
 * in situ carcinoma penile disease penis squamous cell carcinoma carcinoma in situ of male genital organs
 * Human disease
 * DOID:8872
 * penis mixed squamous cell carcinoma
 * class of disease
 * penis squamous cell carcinoma
 * Human disease
 * DOID:8009
 * penis non-invasive verrucous carcinoma
 * class of disease
 * penis verrucous carcinoma penis carcinoma in situ cervical verrucous carcinoma
 * Human disease
 * DOID:5907
 * penis papillary carcinoma
 * class of disease
 * penis squamous cell carcinoma papillary squamous carcinoma
 * Human disease
 * DOID:8013
 * penis sarcoma
 * class of disease
 * penile cancer sarcoma
 * sarcoma and malignant neoplasm of penis that is located in the penis
 * DOID:11838
 * penis squamous cell carcinoma
 * class of disease
 * penis carcinoma squamous cell carcinoma
 * penis carcinoma that has material basis in squamous cells
 * DOID:5518
 * Squamous-cell carcinoma of the penis
 * penis verrucous carcinoma
 * class of disease
 * penis squamous cell carcinoma verrucous carcinoma penis papillary carcinoma
 * Human disease
 * DOID:5908
 * peptic esophagitis
 * class of disease
 * peptic ulcer disease esophagitis gastroesophageal reflux disease
 * human disease
 * DOID:13976
 * C06.405.117.620.420 C06.405.205.663.420 C06.405.469.275.800.523 C06.405.748.586.524
 * peptic ulcer disease
 * class of disease
 * gastrointestinal system disease duodenal disease disease
 * ulcer of an area of the gastrointestinal tract
 * DOID:750
 * C06.405.469.275.800 C06.405.748.586
 * Peptic ulcers
 * Benign gastric ulcer 1.jpg
 * perforated corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10445
 * perforated ulcer
 * class of disease
 * peptic ulcer disease gastric perforation
 * medical condition of the gastrointestinal tract wall
 * DOID:752
 * C06.405.469.275.800.698 C06.405.748.586.698
 * DU 2.jpg
 * perforation of bile duct
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:13409
 * periampullary adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma
 * Human disease
 * DOID:8110
 * periampullary adenoma
 * class of disease
 * ampulla of Vater neoplasm adenoma
 * Human disease
 * DOID:0050849
 * perianal gland tumor
 * class of disease
 * cancer in dogs anus neoplasm
 * dog disease
 * DOID:4550
 * C04.588.083 C04.588.274.476.411.307.790.040.040 C06.301.371.411.307.790.040.040 C06.405.249.411.307.790.040.040 C06.405.469.491.307.790.040.040 C06.405.469.860.101.163.083 C06.405.469.860.180.500.040.040 C22.073
 * perianal hematoma
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9745
 * Perianal hematoma
 * perianal skin Paget's disease
 * class of disease
 * anal margin carcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:7708
 * periapical abscess
 * class of disease
 * periapical periodontitis dental abscess
 * localized collection of pus associated with a tooth
 * DOID:2562
 * C01.539.830.025.650 C07.320.830.700.700 C07.465.714.306.700.700 C07.465.714.533.487.700
 * periapical periodontitis
 * class of disease
 * inflammation periodontitis dental pulp disease periapical disease tooth pathology
 * Human disease
 * DOID:823
 * C07.320.830.700 C07.465.714.306.700 C07.465.714.533.487
 * pericardial effusion
 * class of disease symptom or sign
 * pericardium disease cardiovascular system symptom disease
 * pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
 * DOID:118
 * C14.280.695
 * Pericardial effusion
 * pericardial mesothelioma
 * class of disease
 * pericardium cancer mesothelioma
 * Human disease
 * DOID:6201
 * pericarditis
 * class of disease
 * pericardium disease inflammation inflammatory disease heart disease disease
 * pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
 * DOID:1787
 * C14.280.720
 * Pericarditis
 * Pericarditis10.JPG
 * pericardium cancer
 * class of disease
 * heart cancer neoplasm of pericardium pericardium disease
 * Human disease
 * DOID:116
 * pericardium leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of pericardium pericardium disease cardiovascular organ benign neoplasm
 * Human disease
 * DOID:5137
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * penile urethral cancer
 * class of disease
 * male urethral cancer
 * Human disease
 * DOID:8223
 * penis Paget's disease
 * class of disease
 * penis carcinoma extramammary Paget's disease adenocarcinoma of penis genetic urogenital tumor
 * Human disease
 * DOID:3448
 * Penile Paget's disease
 * penis basal cell carcinoma
 * class of disease
 * penis carcinoma basal-cell carcinoma rare skin disease
 * human disease
 * DOID:4277
 * penis basaloid carcinoma
 * class of disease
 * penis squamous cell carcinoma basaloid squamous cell carcinoma
 * Human disease
 * DOID:7047
 * penis carcinoma
 * class of disease
 * penile cancer carcinoma
 * penile cancer that is located in the skin or tissues of the penis
 * DOID:3449
 * penis carcinoma in situ
 * class of disease
 * in situ carcinoma penile disease penis squamous cell carcinoma carcinoma in situ of male genital organs
 * Human disease
 * DOID:8872
 * penis mixed squamous cell carcinoma
 * class of disease
 * penis squamous cell carcinoma
 * Human disease
 * DOID:8009
 * penis non-invasive verrucous carcinoma
 * class of disease
 * penis verrucous carcinoma penis carcinoma in situ cervical verrucous carcinoma
 * Human disease
 * DOID:5907
 * penis papillary carcinoma
 * class of disease
 * penis squamous cell carcinoma papillary squamous carcinoma
 * Human disease
 * DOID:8013
 * penis sarcoma
 * class of disease
 * penile cancer sarcoma
 * sarcoma and malignant neoplasm of penis that is located in the penis
 * DOID:11838
 * penis squamous cell carcinoma
 * class of disease
 * penis carcinoma squamous cell carcinoma
 * penis carcinoma that has material basis in squamous cells
 * DOID:5518
 * Squamous-cell carcinoma of the penis
 * penis verrucous carcinoma
 * class of disease
 * penis squamous cell carcinoma verrucous carcinoma penis papillary carcinoma
 * Human disease
 * DOID:5908
 * peptic esophagitis
 * class of disease
 * peptic ulcer disease esophagitis gastroesophageal reflux disease
 * human disease
 * DOID:13976
 * C06.405.117.620.420 C06.405.205.663.420 C06.405.469.275.800.523 C06.405.748.586.524
 * peptic ulcer disease
 * class of disease
 * gastrointestinal system disease duodenal disease disease
 * ulcer of an area of the gastrointestinal tract
 * DOID:750
 * C06.405.469.275.800 C06.405.748.586
 * Peptic ulcers
 * Benign gastric ulcer 1.jpg
 * perforated corneal ulcer
 * class of disease
 * corneal ulcer
 * Human disease
 * DOID:10445
 * perforated ulcer
 * class of disease
 * peptic ulcer disease gastric perforation
 * medical condition of the gastrointestinal tract wall
 * DOID:752
 * C06.405.469.275.800.698 C06.405.748.586.698
 * DU 2.jpg
 * perforation of bile duct
 * class of disease
 * biliary tract disease
 * Human disease
 * DOID:13409
 * periampullary adenocarcinoma
 * class of disease
 * ampulla of Vater adenocarcinoma
 * Human disease
 * DOID:8110
 * periampullary adenoma
 * class of disease
 * ampulla of Vater neoplasm adenoma
 * Human disease
 * DOID:0050849
 * perianal gland tumor
 * class of disease
 * cancer in dogs anus neoplasm
 * dog disease
 * DOID:4550
 * C04.588.083 C04.588.274.476.411.307.790.040.040 C06.301.371.411.307.790.040.040 C06.405.249.411.307.790.040.040 C06.405.469.491.307.790.040.040 C06.405.469.860.101.163.083 C06.405.469.860.180.500.040.040 C22.073
 * perianal hematoma
 * class of disease
 * hemorrhoid
 * Human disease
 * DOID:9745
 * Perianal hematoma
 * perianal skin Paget's disease
 * class of disease
 * anal margin carcinoma extramammary Paget's disease anal Paget's disease
 * Human disease
 * DOID:7708
 * periapical abscess
 * class of disease
 * periapical periodontitis dental abscess
 * localized collection of pus associated with a tooth
 * DOID:2562
 * C01.539.830.025.650 C07.320.830.700.700 C07.465.714.306.700.700 C07.465.714.533.487.700
 * periapical periodontitis
 * class of disease
 * inflammation periodontitis dental pulp disease periapical disease tooth pathology
 * Human disease
 * DOID:823
 * C07.320.830.700 C07.465.714.306.700 C07.465.714.533.487
 * pericardial effusion
 * class of disease symptom or sign
 * pericardium disease cardiovascular system symptom disease
 * pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
 * DOID:118
 * C14.280.695
 * Pericardial effusion
 * pericardial mesothelioma
 * class of disease
 * pericardium cancer mesothelioma
 * Human disease
 * DOID:6201
 * pericarditis
 * class of disease
 * pericardium disease inflammation inflammatory disease heart disease disease
 * pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
 * DOID:1787
 * C14.280.720
 * Pericarditis
 * Pericarditis10.JPG
 * pericardium cancer
 * class of disease
 * heart cancer neoplasm of pericardium pericardium disease
 * Human disease
 * DOID:116
 * pericardium leiomyoma
 * class of disease
 * leiomyoma benign neoplasm of pericardium pericardium disease cardiovascular organ benign neoplasm
 * Human disease
 * DOID:5137
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * pericholangitis
 * class of disease
 * ascending cholangitis primary sclerosing cholangitis
 * Human disease
 * DOID:14272
 * perichondritis of auricle
 * class of disease
 * otitis externa acquired deformities of the ear
 * Human disease
 * DOID:222
 * Perichondritis
 * pericoronitis
 * class of disease
 * gingival disease
 * human disease
 * DOID:3671
 * C07.465.714.258.771
 * Pericoronitis
 * periductal breast myoepitheliosis
 * class of disease
 * breast myoepitheliosis
 * Human disease
 * DOID:7520
 * perinatal intestinal perforation
 * class of disease
 * intestinal perforation perinatal digestive system disorder
 * Human disease
 * DOID:2073
 * perinatal jaundice due to hepatocellular damage
 * class of disease
 * neonatal jaundice Neonatal hepatitis
 * Human disease
 * DOID:11452
 * perineocele
 * class of disease
 * pelvic organ prolapse
 * human disease
 * DOID:12637
 * perinephritis
 * class of disease
 * kidney disease inflammatory disease connective tissue disease
 * human disease
 * DOID:2982
 * C12.777.419.685 C13.351.968.419.685
 * perineural angioma
 * class of disease
 * deep angioma hemangioma central nervous system organ benign neoplasm
 * Human disease
 * DOID:8331
 * perineurioma
 * class of disease
 * nerve sheath neoplasms
 * Human disease
 * DOID:4697
 * Perineuroma
 * periocular meningioma
 * class of disease
 * meningioma intraorbital meningioma
 * Human disease
 * DOID:8030
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * periodic limb movement disorder
 * class of disease symptom or sign
 * sleep disorder disease
 * sleep disorder that involves involuntary limb movement during sleep
 * DOID:9207
 * C10.886.425.800.600 C10.886.659.618
 * periodontal disease
 * class of disease
 * tooth pathology jaw disease disease
 * human disease
 * DOID:3388
 * C07.465.714
 * Gingivitis (crop).jpg
 * periodontitis
 * class of disease
 * periodontal disease disease
 * gum disease
 * DOID:824
 * C07.465.714.533
 * Periodontitis
 * Paro1.JPG
 * periodontosis
 * class of disease
 * periodontal disease tooth pathology
 * human disease
 * DOID:9893
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * periosteal chondrosarcoma
 * class of disease
 * chondrosarcoma
 * Human disease
 * DOID:5859
 * periosteal osteogenic sarcoma
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * class of disease
 * peripheral osteosarcoma
 * Human disease
 * DOID:6489
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * periostitis
 * ''[[:d:Q112193867|class of disea
 * periostitis
 * ''[[:d:Q112193867|class of disea