Category:Williams syndrome

From Wikimedia Commons, the free media repository
Jump to navigation Jump to search
síndrome de Williams (es); 威廉氏綜合症 (yue); Williams-szindróma (hu); Williams-heilkenni (is); Синдром Вильямса (ru); Syndrom Williams (cy); Ուիլյամսի համախտանիշ (hy); 威廉氏症候群 (zh); Williams syndrom (da); ვილიამსის სინდრომი (ka); ウィリアムズ症候群 (ja); Williams syndrom (sv); תסמונת ויליאמס (he); Williamsin oireyhtymä (fi); sindromo de Williams (eo); Вилијамс синдром (mk); வில்லியம்ஸ் நோய்க்கூட்டறிகுறி (ta); sindrome di Williams-Beuren (it); syndrome de Williams (fr); Williamsi sündroom (et); Hội chứng Williams (vi); síndrome de Williams (ca); Viljamso sindromas (lt); نشانگان ویلیامز (fa); síndrome de Williams (pt); Williams-Beuren-Syndrom (de); синдром Вільямса (uk); กลุ่มอาการวิลเลียม (th); Zespół Williamsa (pl); Williams syndrom (nb); Syndroom van Williams (nl); Williams sendromu (tr); Sindrom Williams (ms); ଉଇଲିଅମସ ସିଣ୍ଡ୍ରୋମ (or); Sindrom Williams (id); Williams-Beuren syndrome (en); متلازمة ويليام (ar); σύνδρομο Williams (el); Williamsův syndrom (cs) malattia umana (it); תסמונת גנטית נדירה, הנגרמת בגלל פגיעה כרומוזומלית (he); Krankheit (de); νευροαναπτυξιακή διαταραχή (el); neurodevelopmental disorder (en); متلازمة الحب المطلق (ar); genetická choroba (cs); genetycznie uwarunkowana choroba (pl) sindrome di Williams (it); வில்லியம் நோய்க்கூட்டறிகுறி (ta); Syndrome de Williams-Beuren, Syndrome de Williams Beuren (fr); Sindrome de Williams, Sindrome de Williams Beuren, Síndrome de Williams-Beuren, Síndrome de Williams Beuren, Sindrome de Williams-Beuren (es); Williams syndrome (th); Zespół Williamsa i Beurena, Zespół Williamsa-Beurena (pl); Вільямса синдром (uk); Williams-syndroom, Williams-Beuren-Syndroom, Williams-Beurensyndroom, Williamssyndroom, Williamssyndrooom, Williams-Beuren syndroom, Williams syndroom (nl); Лицо эльфа, Синдром лица эльфа, Вильямса синдром, Синдром Уильямса (ru); תסמונת וויליאמס (he); Fanconi-Schlesiner-Syndrom, Idiopathische Hyperkalzämie, Williams-Syndrom, Williams Syndrom, Elfin-face-Syndrom (de); Williamsin syndrooma, Williams-Beurenin oireyhtymä, Williams-Beurenin syndrooma (fi); Fanconi Schlesinger syndrome, Williams–Beuren syndrome, WBS, Williams Syndrome, WS, Chromosome 7Q11.23 Deletion Syndrome, 1.5- to 1.8-Mb, Monosomy 7q11.23, WILLIAMS-BEUREN SYNDROME; WBS, WBS, Williams-Beuren Syndrome (WBS), WILLIAMS-BEUREN SYNDROME, Deletion 7q11.23 (en); sindromo de Williams-Beuren (eo); Williams-Beureni sündroom, WS, Williamsi-Beureni sündroom, WBS (et); Viljamso Beureno sindromas, Viljamso beureno (lt)
Williams-Beuren syndrome 
neurodevelopmental disorder
Williams syndromeCCBY.jpg
Upload media
Wikipedia-logo-v2.svg  Wikipedia
Instance ofdisease,
developmental defect during embryogenesis,
rare disease,
designated intractable/rare diseases
Subclass ofchromosomal deletion syndrome,
supravalvular aortic stenosis,
syndromic developmental defect of the eye,
multiple congenital anomalies/dysmorphic syndrome-intellectual disability,
malformation syndrome with short stature,
genetic hypertension,
partial deletion of the long arm of chromosome 7,
rare syndrome with cardiac malformations,
rare abdominal surgical disease,
genetic syndromic intellectual disability,
organic brain syndrome,
syndromic epicanthus,
motor stereotypies
Named after
  • John Cyprian Phipps Williams
Discoverer or inventor
  • John Cyprian Phipps Williams
Authority control
Edit infobox data on Wikidata

Subcategories

This category has only the following subcategory.