Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/8

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 * 1) Microbrachycephaly ptosis cleft lip
 * 2) Microcephaly hypergonadotropic hypogonadism short stature
 * 3) Microcephaly mental retardation retinopathy
 * 4) Microcephaly mental retardation spasticity epilepsy
 * 5) Microcephaly microcornea syndrome Seemanova type
 * 6) Microcephaly micropenis convulsions
 * 7) Microcephaly seizures mental retardation heart disorders
 * 8) Microcephaly, holoprosencephaly, and intrauterine growth retardation
 * 9) Microcornea corectopia macular hypoplasia
 * 10) Microdontia hypodontia short stature
 * 11) Microgastria limb reduction defect
 * 12) Microgastria short stature diabetes
 * 13) Micromelic dysplasia dislocation of radius
 * 14) Microsomia hemifacial radial defects
 * 15) Midline defects autosomal type
 * 16) Midline defects recessive type
 * 17) Midline developmental field defects
 * 18) Midline field defects
 * 19) Mievis Verellen Dumoulin syndrome
 * 20) Milner Khallouf Gibson syndrome
 * 21) Minoxidil antenatal infection
 * 22) Mirror hands feet nasal defects
 * 23) Mitochondrial PEPCK deficiency
 * 24) Miura syndrome
 * 25) Mixed sclerosing bone dystrophy
 * 26) Moebius axonal neuropathy hypogonadism
 * 27) Moisture-associated skin damage (MASD). "The four specific types of moisture-associated skin damage that will be discussed here are periwound moisture-associated dermatitis, peristomal moisture-associated dermatitis, incontinence-associated dermatitis, and intertriginous dermatitis."https://www.woundsource.com/patientcondition/moisture-associated-skin-damage-masd
 * 28) Mollica Pavone Antener syndrome
 * 29) Monodactyly tetramelic
 * 30) Mononen Karnes Senac syndrome
 * 31) Monosomy 8q12 21
 * 32) Monosomy 8q21 q22
 * 33) Montefiore syndrome
 * 34) Moore Smith Weaver syndrome
 * 35) Morgani Turner Albright syndrome
 * 36) Morillo Cucci Passarge syndrome
 * 37) Morrison Young syndrome
 * 38) Motor neuro-ophthalmic disorders
 * 39) Motor neuropathy peripheral dysautonomia
 * 40) MSBD syndrome
 * 41) Muller Barth Menger syndrome
 * 42) Mullerian derivatives lymphangiectasia polydactyly
 * 43) Mulliez Roux Loterman syndrome
 * 44) Multifocal heterotopia
 * 45) Multinodular goiter cystic kidney polydactyly
 * 46) Multiple congenital anomalies mental retardation, growth failure and cleft lip palate
 * 47) Multiple joint dislocations metaphyseal dysplasia
 * 48) Multiple pterygium syndrome lethal type
 * 49) Multiple synostoses syndrome 1
 * 50) Multiple vertebral anomalies unusual facies
 * 51) Muscular fibrosis multifocal obstructed vessels
 * 52) Myelofibrosis-osteosclerosis
 * 53) Myeloid splenomegaly
 * 54) Myhre Ruvalcaba Kelley syndrome
 * 55) Myhre School syndrome
 * 56) Myoclonus ataxia
 * 57) Myoclonus cerebellar ataxia deafness
 * 58) Myofibrillar lysis
 * 59) Myopathy cataract hypogonadism
 * 60) Myopathy growth and mental retardation hypospadias
 * 61) Myopathy ophthalmoplegia hypoacousia areflexia
 * 62) Myopathy with lysis of myofibrils
 * 63) Myotonia mental retardation skeletal anomalies
 * 64) N syndrome
 * 65) N-acetyl-alpha-D-galactosaminidase
 * 66) NADH CoQ reductase, deficiency of
 * 67) NADH cytochrome B5 reductase deficiency
 * 68) Narrow oral fissure short stature cone shaped epiphyses
 * 69) Nasopalpebral lipoma coloboma syndrome
 * 70) Nasopharyngeal teratoma Dandy Walker diaphragmatic hernia
 * 71) Natal teeth intestinal pseudoobstruction patent ductus
 * 72) Nephronophthisis familial adult spastic quadriparesis
 * 73) Nephropathy deafness hyperparathyroidism
 * 74) Nephropathy familial with hyperuricemia
 * 75) Nephropathy, familial with gout
 * 76) Nephrosis deafness urinary tract digital malformation
 * 77) Nephrotic syndrome ocular anomalies
 * 78) Neuhauser Daly Magnelli syndrome
 * 79) Neuhauser Eichner Opitz syndrome
 * 80) Neural crest tumor
 * 81) Neurofaciodigitorenal syndrome
 * 82) Neuronal intranuclear hyaline inclusion disease
 * 83) Neuronal intranuclear inclusion disease
 * 84) Neutropenia monocytopenia deafness
 * 85) Nevus of ota retinitis pigmentosa
 * 86) Night blindness skeletal anomalies unusual facies
 * 87) Nivelon Nivelon Mabille syndrome
 * 88) Noble Bass Sherman syndrome
 * 89) Nonmedullary thyroid carcinoma, with cell oxyphilia
 * 90) Noonan like syndrome
 * 91) Nova syndrome
 * 92) Novak syndrome
 * 93) O Doherty syndrome
 * 94) Ocular convergence spasm
 * 95) Oculo cerebro acral syndrome
 * 96) Oculo cerebro osseous syndrome
 * 97) Oculo digital syndrome
 * 98) Oculo skeletal renal syndrome
 * 99) Oculo tricho anal syndrome
 * 100) Oculo tricho dysplasia
 * 101) Oculocerebral hypopigmentation syndrome type Preus
 * 102) Oculodental syndrome Rutherfurd syndrome
 * 103) Oculo-gastrointestinal muscular dystrophy
 * 104) Oculomaxillofacial dysostosis
 * 105) Oculomaxillofacial dysplasia with oblique facial clefts
 * 106) Oculorenocerebellar syndrome
 * 107) Odonto onycho dysplasia with alopecia
 * 108) Odontomicronychial dysplasia
 * 109) Odontotrichomelic hypohidrotic dysplasia
 * 110) OFD syndrome type 8
 * 111) OFD syndrome type Figuera
 * 112) Oligodactyly tetramelic postaxial
 * 113) Omodysplasia type 1
 * 114) Omphalocele cleft palate syndrome lethal
 * 115) Omphalomesenteric cyst
 * 116) Onat syndrome
 * 117) Ophthalmomandibulomelic dysplasia
 * 118) Ophthalmoplegia mental retardation lingua scrotalis
 * 119) Opitz Mollica Sorge syndrome
 * 120) Opitz Reynolds Fitzgerald syndrome
 * 121) Oral facial digital syndrome type 4
 * 122) Oral-facial-digital syndrome, type IV
 * 123) Oro acral syndrome
 * 124) Orofaciodigital syndrome Gabrielli type
 * 125) Orofaciodigital syndrome Shashi type
 * 126) Orofaciodigital syndrome Thurston type
 * 127) Orofaciodigital syndrome type 2
 * 128) Ossicular Malformations, familial
 * 129) Osteoarthropathy of fingers familial
 * 130) Osteochondrodysplasia thrombocytopenia hydrocephalus
 * 131) Osteocraniostenosis
 * 132) Osteodysplastic dwarfism Corsello type
 * 133) Osteolysis syndrome recessive
 * 134) Osteopathia striata pigmentary dermopathy white forelock
 * 135) Osteoporosis macrocephaly mental retardation blindness
 * 136) Osteoporosis oculocutaneous hypopigmentation syndrome
 * 137) Osteosarcopenia (combined bone & muscle decline in aged)
 * 138) Otoonychoperoneal syndrome
 * 139) Ouvrier Billson syndrome
 * 140) Ovarian dwarfism
 * 141) Overfolded helix
 * 142) Overgrowth radial ray defect arthrogryposis