User:Rollcloud

Hey guy, welcome to my English Wikipedia user page

Check out my Wikimedia Commons gallery: https://commons.wikimedia.org/wiki/User:Rollcloud

My Spanish Wikipedia user page: https://es.wikipedia.org/wiki/Usuario:Rollcloud

I mostly spend my time here making small edits and creating articles

Articles: User:Rollcloud/articles

Links
Pages for easy access when I need them

https://en.m.wikipedia.org/wiki/Template:Infobox_medical_condition

https://en.m.wikipedia.org/wiki/User:Rollcloud/sandbox

https://en.m.wikipedia.org/wiki/List_of_African_countries_by_population

https://en.m.wikipedia.org/wiki/List_of_Asian_countries_by_population

https://en.m.wikipedia.org/wiki/List_of_Middle_Eastern_countries_by_population

https://en.m.wikipedia.org/wiki/Countries_of_the_United_Kingdom

List of random contributions
Contributions I compile for myself to look back on later

https://en.m.wikipedia.org/wiki/Special:MobileDiff/875345291?diffmode=visual#Citations

Articles
This is a list of articles I have created

I don't claim ownership over any of these articles, WP:Ownership

(In order from first to most recent article)

- Stratocumulus castellanus cloud

- Altocumulus lacunosus cloud

- Stratus silvagenitus

- Cumulonimbus cauda

- Altocumulus volutus

- Stratocumulus lenticularis

- Translucidus (cloud variety)

- Opacus (cloud variety)

- Perlucidus (cloud variety)

- Hitchhiker's thumb

- Stratocumulus lenticularis

- Dolichonychia

- Brachyphalangy

- Brachymetacarpia

- Polyonychia

- 7p22.1 microduplication syndrome

- Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome

- Nestor-Guillermo progeria syndrome

- Guizar–Vasquez–Sanchez–Manzano syndrome

- Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome

- Stocco dos Santos syndrome

- Infantile cerebellar retinal degeneration

- North Carolina macular dystrophy

- Hamanishi Ueba Tsuji syndrome

- Amish lethal microcephaly

- Dilated cardiomyopathy with ataxia syndrome

- Microcephaly deafness syndrome

- Familial thoracic aortic aneurysm and aortic dissection

- Hair defect-photosensitivity-intellectual disability syndrome

- Familial opposable triphalangeal thumbs duplication

- Cousin–Walbraum–Cegarra syndrome

- Fine-Lubinsky syndrome

- Ichthyosis-intellectual disability-dwarfism-renal impairment

- Reardon-Hall-Slaney syndrome

- Autosomal dominant cerebellar ataxia, deafness, and narcolepsy

- Lubani Al Saleh Teebi syndrome

- Ostravik-Lindemann-Solberg syndrome

- Bifid nose

- Thai symphalangism syndrome

- Camptodactyly-taurinuria syndrome

- Microcephalic primordial dwarfism, Montreal type

- Say-Field-Coldwell syndrome

- Morse-Rawnsley-Sargent syndrome

- Ectrodactyly with tibia aplasia/hypoplasia

- Thumb stiffness-brachydactyly-intellectual disability syndrome

- Boudhina-Yedes-Khiari syndrome

- Macdermot-Winter syndrome

- Van De Berghe Dequeker syndrome

- Fibular aplasia-ectrodactyly syndrome

- Autosomal dominant partial epilepsy with auditory features

- Kozlowski-Krajewska syndrome

- Ulnar dysplasia

- Hirschsprung's disease-type D brachydactyly syndrome

- Lowry-Wood syndrome

- Al Gazali Sabrinathan Nair syndrome

- Verloes Van Maldergem Marneffe syndrome

- Feigenbaum-Bergeron-Richardson syndrome

- Camptodactyly, tall stature, and hearing loss syndrome

- Weyer's ulnar ray/oligodactyly syndrome

- Juvenile-onset dystonia

- IVIC syndrome

- Sergio Arias Cazorla

- Viljoen-Kallis-Voges syndrome

- Absence of fingerprints-congenital milia syndrome

- Tel Hashomer camptodactyly syndrome

- Saito-Kuba-Tsuruta syndrome

- Anophthalmia megalocornea cardiopathy skeletal anomalies syndrome

- Chudley-Mccullough syndrome

- Cleft palate short stature vertebral anomalies syndrome

- Leigh syndrome, French Canadian type

- Al-Gazali-Donnai-Mueller syndrome

- Multiple congenital anomalies-hypotonia-seizures syndrome

- Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome

- Brachydactyly-long thumb syndrome

- Du Pan syndrome

- Deafness-vitiligo-achalasia syndrome

- Aortic arch anomaly - peculiar facies - intellectual disability

- Adolescent idiopathic scoliosis

- Isolated hyperCKemia

- Acanthosis nigricans-muscle cramps-acral enlargement syndrome

- Blepharoptosis-myopia-ectopia lentis syndrome

- Autosomal recessive axonal neuropathy with neuromyotonia

- Heart-hand syndrome, Spanish type

- Gustavson syndrome

- Brachial amelia, cleft lip, and holoprosencephaly

- Familial osteodysplasia, Anderson type

- Camera-Marugo-Cohen syndrome

- Santos-Mateus-Leal syndrome

- Cataract-ataxia-deafness syndrome

- Cryptorchidism-arachnodactyly-intellectual disability syndrome

- Spondylometaphyseal dysplasia, East-African type

- Waardenburg anophthalmia syndrome

- Thickened earlobes-conductive deafness syndrome

- Absent tibia-polydactyly-arachnoid cyst syndrome

- Dauwerse-Peters syndrome

- Infantile spasms-broad thumbs syndrome

- Spondylocamptodactyly

- Retinal cone dystrophy 3B

- Polydactyly-myopia syndrome

- PURA syndrome

- Acro-oto-radial syndrome

- Blepharophimosis intellectual disability syndromes

- Combarros-Calleja-Leno syndrome

- Kirner's deformity

- Familial dwarfism and painful muscle spasms

- Familial multiple cafe-au-lait spots

- St. Helena familial genu valgum

- Polymetatarsia

- Familial episodic pain syndrome

- Ectrodactyly-polydactyly syndrome

- Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome

- Tucker syndrome

- Otofaciocervical syndrome

- GATAD2B-associated neurodevelopmental disorder

- Distichiasis, congenital heart defects and mixed peripheral vascular anomalies

- Angel-shaped phalango-epiphyseal dysplasia

- Skin fragility-woolly hair-palmoplantar keratoderma syndrome

- Tranebjaerg-Svejgaard syndrome

- PRICKLE1-related progressive myoclonus epilepsy with ataxia

- Sudden infant death with dysgenesis of the testes syndrome

- Acrocraniofacial dysostosis

- Autism with port-wine stain syndrome

- Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly

- Microcornea, glaucoma, and absent frontal sinuses

- Boucher-Neuhäuser syndrome

- Growth delay-hydrocephaly-lung hypoplasia syndrome

- Metacarpal synostosis

- Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

- Gollop-Wolfgang complex

- Absence deformity of leg-cataract syndrome

- Early-onset parkinsonism-intellectual disability syndrome

- X-linked sideroblastic anemia and spinocerebellar ataxia

- Scalp defects-postaxial polydactyly syndrome

- Mirror polydactyly-vertebral segmentation-limb defects syndrome

- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

- Cerebro-costo-mandibular syndrome

- Aplasia cutis congenita-intestinal lymphangiectasia syndrome

- Trigonocephaly-bifid nose-acral anomalies syndrome

- Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome

- Cardiospondylocarpofacial syndrome

- Dwarfism, low-birth-weight type with unresponsiveness to growth hormone

- Pai syndrome

- Amaurosis congenita, cone-rod type, with congenital hypertrichosis

- Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa

- McDonough syndrome

- Ulna hypoplasia-intellectual disability syndrome

- Proud syndrome

- Megalocornea-intellectual disability syndrome

- Iris hypoplasia with glaucoma

- Triphalangeal thumbs-brachyectrodactyly syndrome

- Marsili syndrome

- Pierre Robin sequence-faciodigital anomaly syndrome

- GOSR2-related progressive myoclonus ataxia

- Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons

- Palmoplantar keratoderma with deafness

- FBXW7 neurodevelopmental syndrome

- CHAMP1-associated intellectual disability syndrome

- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome

- Curry-Jones syndrome

- Meacham syndrome

- Small patella syndrome

- CAPOS syndrome

- Coloboma of macula-brachydactyly type B syndrome

- Split hand split foot-nystagmus syndrome

- GRIN2B-related neurodevelopmental disorder

- Spastic paraplegia 6

- Brachydactyly-preaxial hallux varus syndrome

- Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome

- Short-limb skeletal dysplasia with severe combined immunodeficiency

- Osteopathia striata with cranial sclerosis

- Czech dysplasia, metatarsal type

- Osteoporosis-pseudoglioma syndrome

- Collins-Pope syndrome

- Intellectual disability-spasticity-ectrodactyly syndrome

- Hypomyelination-congenital cataract syndrome

- Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly

- Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia syndrome

- Olivopontocerebellar atrophy-deafness syndrome

- Mandibulofacial dysostosis-microcephaly syndrome

- X-linked cone-rod dystrophy, type 1

- Familial nasal acilia

- Autosomal recessive isolated ectopia lentis

- Familial benign copper deficiency

- Spastic paraplegia 31

- X-linked Charcot-Marie-Tooth disease

- Splenogonadal fusion-limb defects-micrognathia syndrome

- Autosomal recessive bestrophinopathy

- Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome

- Schneckenbecken dysplasia

- Heart-hand syndrome, Slovenian type

- Goldmann-Favre syndrome

- Spondylometaphyseal dysplasia with cone-rod dystrophy

- Y-linked deafness, type 1

- Corneal dystrophy-perceptive deafness syndrome

- Thoracic dysplasia-hydrocephalus syndrome

- Syndactyly-nystagmus syndrome due to 2q31.1 microduplication

- Familial cutaneous collagenoma

- Craniofacial dysostosis-diaphyseal hyperplasia syndrome

- Oculopharyngodistal myopathy

- Conductive deafness-ptosis-skeletal anomalies syndrome

- Autosomal dominant leukodystrophy with autonomic disease

- Odontoonychodermal dysplasia

- SLC35A1-CDG

- Dermatoosteolysis, Kirghizian type

- Familial synovial chondromatosis with dwarfism

- Cyprus facial neuromusculoskeletal syndrome

- Hall-Riggs syndrome

- Hereditary neurocutaneous angioma

- Severe intellectual disability-progressive spastic diplegia syndrome

- Histidinuria renal tubular defect syndrome

- X-linked complicated corpus callosum dysgenesis

- Pulmonary atresia with ventricular septal defect

- Sonoda syndrome

- Graham–Boyle–Troxell syndrome

- Cochleosaccular degeneration with progressive cataracts

- Aplasia cutis-myopia syndrome

- Pyknoachondrogenesis

- Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome

- Hypohidrotic ectodermal dysplasia with immune deficiency

- Keratosis follicularis-dwarfism-cerebral atrophy syndrome

- Porencephaly-cerebellar hypoplasia-internal malformations syndrome

- Ankylosing vertebral hyperostosis with tylosis

- Rs16891982

- Wolfram-like syndrome

- Salt and pepper syndrome

- Calvarial doughnut lesions-bone fragility syndrome

- Familial natural short sleep

- SOFT syndrome

- Compton-North congenital myopathy

- Radio-renal syndrome

- Spondyloenchondrodysplasia

- Faciocardiorenal syndrome

- Progressive bifocal chorioretinal atrophy

- Isolated hyperchlorhidrosis

- Lymphedema-posterior choanal atresia syndrome