Category:Williams syndrome

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Williams-Beuren syndrome 
neurodevelopmental disorder
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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
  • J.C.P. Williams
Discoverer or inventor
  • J.C.P. Williams
Authority control
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síndrome de Williams (es); Williams-szindróma (hu); Williams-heilkenni (is); Синдром Вильямса (ru); Syndrom Williams (cy); نشانگان ویلیامز (fa); 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); வில்லியம்ஸ் நோய்க்கூட்டறிகுறி (ta); sindrome di Williams-Beuren (it); syndrome de Williams (fr); Williamsi sündroom (et); Hội chứng Williams (vi); Viljamso sindromas (lt); síndrome de Williams (ca); síndrome de Williams (pt); Williams-Beuren-Syndrom (de); Ուիլյամսի համախտանիշ (hy); Sindrom Williams (id); Zespół Williamsa (pl); Williams syndrom (nb); Syndroom van Williams (nl); синдром Вільямса (uk); Williams sendromu (tr); Sindrom Williams (ms); ଉଇଲିଅମସ ସିଣ୍ଡ୍ରୋମ (or); Williams-Beuren syndrome (en); متلازمة ويليام (ar); σύνδρομο Williams (el); กลุ่มอาการวิลเลียม (th) malattia umana (it); Krankheit (de); neurodevelopmental disorder (en); genetycznie uwarunkowana choroba (pl); νευροαναπτυξιακή διαταραχή (el); תסמונת גנטית נדירה, הנגרמת בגלל פגיעה כרומוזומלית (he) 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)


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