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
| Wikipedia:Babel | ||
|---|---|---|
| ||
| Search user languages |
 | This user has an alternative account named Doggo29393 (talk · contribs). |
| This user has an alternative account named Bongbung (talk · contribs). |
Links
[edit]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
[edit]Contributions I compile for myself to look back on later
https://en.m.wikipedia.org/wiki/Special:MobileDiff/875345291?diffmode=visual#Citations
Articles
[edit]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
- Translucidus (cloud variety)
- 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
- Infantile cerebellar retinal degeneration
- North Carolina macular dystrophy
- Hamanishi Ueba Tsuji syndrome
- 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
- 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
- Camptodactyly-taurinuria syndrome
- Microcephalic primordial dwarfism, Montreal type
- Morse-Rawnsley-Sargent syndrome
- Ectrodactyly with tibia aplasia/hypoplasia
- Thumb stiffness-brachydactyly-intellectual disability syndrome
- Boudhina-Yedes-Khiari syndrome
- Van De Berghe Dequeker syndrome
- Fibular aplasia-ectrodactyly syndrome
- Autosomal dominant partial epilepsy with auditory features
- Kozlowski-Krajewska syndrome
- Hirschsprung's disease-type D brachydactyly 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
- Viljoen-Kallis-Voges syndrome
- Absence of fingerprints-congenital milia syndrome
- Tel Hashomer camptodactyly syndrome
- Anophthalmia megalocornea cardiopathy skeletal anomalies 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
- Deafness-vitiligo-achalasia syndrome
- Aortic arch anomaly - peculiar facies - intellectual disability
- Adolescent idiopathic scoliosis
- Acanthosis nigricans-muscle cramps-acral enlargement syndrome
- Blepharoptosis-myopia-ectopia lentis syndrome
- Autosomal recessive axonal neuropathy with neuromyotonia
- Heart-hand syndrome, Spanish type
- Brachial amelia, cleft lip, and holoprosencephaly
- Familial osteodysplasia, Anderson type
- Camera-Marugo-Cohen 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
- Infantile spasms-broad thumbs syndrome
- Blepharophimosis intellectual disability syndromes
- Combarros-Calleja-Leno syndrome
- Familial dwarfism and painful muscle spasms
- Familial multiple cafe-au-lait spots
- St. Helena familial genu valgum
- Familial episodic pain syndrome
- Ectrodactyly-polydactyly syndrome
- Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus 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
- Autism with port-wine stain syndrome
- Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly
- Microcornea, glaucoma, and absent frontal sinuses
- Growth delay-hydrocephaly-lung hypoplasia syndrome
- Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- 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
- Amaurosis congenita, cone-rod type, with congenital hypertrichosis
- Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
- Ulna hypoplasia-intellectual disability syndrome
- Megalocornea-intellectual disability syndrome
- Iris hypoplasia with glaucoma
- Triphalangeal thumbs-brachyectrodactyly 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
- Coloboma of macula-brachydactyly type B syndrome
- Split hand split foot-nystagmus syndrome
- GRIN2B-related neurodevelopmental disorder
- 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
- 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
- Autosomal recessive isolated ectopia lentis
- Familial benign copper deficiency
- X-linked Charcot-Marie-Tooth disease
- Splenogonadal fusion-limb defects-micrognathia syndrome
- Autosomal recessive bestrophinopathy
- Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome
- Heart-hand syndrome, Slovenian type
- Spondylometaphyseal dysplasia with cone-rod dystrophy
- 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
- Dermatoosteolysis, Kirghizian type
- Familial synovial chondromatosis with dwarfism
- Cyprus facial neuromusculoskeletal 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
- Graham–Boyle–Troxell syndrome
- Cochleosaccular degeneration with progressive cataracts
- Aplasia cutis-myopia syndrome
- 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
- Calvarial doughnut lesions-bone fragility syndrome
- Familial natural short sleep
- Compton-North congenital myopathy