Category:Williams syndrome

**Williams-Beuren syndrome**
	neurodevelopmental disorder
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Instance of	developmental defect during embryogenesis; rare disease; designated intractable/rare disease; class of disease;
Subclass of	chromosomal 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; syndrome; autosomal dominant disease; disease;
Named after	John Cyprian Phipps Williams;
Discoverer or inventor	John Cyprian Phipps Williams;
Authority file
	Q558077; GND ID: 4323165-2; Library of Congress authority ID: sh98004230; Bibliothèque nationale de France ID: 13540439d; NDL Authority ID: 01196757; BNCF Thesaurus ID: 5062; NL CR AUT ID: ph637817; J9U ID: 987007532654405171
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<nowiki>síndrome de Williams; 威廉氏綜合症; Williams-szindróma; Williams-heilkenni; Синдром Вильямса; Williams-Beuren-Syndrom; نشانگان ویلیامز; 威廉氏症候群; Williams syndrom; ვილიამსის სინდრომი; ウィリアムズ症候群; Williams syndrom; תסמונת ויליאמס; Williamsin oireyhtymä; sindromo de Williams; Вилијамсов синдром; வில்லியம்ஸ் நோய்க்கூட்டறிகுறி; sindrome di Williams-Beuren; syndrome de Williams; Williamsi sündroom; síndrome de Williams; 윌리엄스 증후군; Williamsův syndrom; síndrome de Williams; Viljamso sindromas; синдром Вільямса; Williams sendromu; Вилијамсов синдром; Williams-Beurenov sindrom; Sindrom Williams; ଉଇଲିଅମସ ସିଣ୍ଡ୍ରୋମ; Syndroom van Williams; Sindrom Williams; Zespół Williamsa; Williams syndrom; Vilyams sindromu; กลุ่มอาการวิลเลียม; Syndrom Williams; Hội chứng Williams; Ուիլյամսի համախտանիշ; Williams-Beuren syndrome; متلازمة ويليام; σύνδρομο Ουίλιαμς; Williamsov sindrom; malattia umana; l’association d’un retard mental, d’une cardiopathie congénitale, d’un faciès et d’un comportement hypersocial caractéristiques de l’individu affecté; genetická choroba; trastorno genético; genetycznie uwarunkowana choroba; תסמונת גנטית נדירה, הנגרמת בגלל פגיעה כרומוזומלית; medische conditie; متلازمة الحب المطلق; хвороба; Krankheit; geneettinen häiriö; neurodevelopmental disorder; وضعیت پزشکی; νευροαναπτυξιακή διαταραχή; nevrorazvojni sindrom; sindrome di Williams; Syndrome de Williams-Beuren; Syndrome de Williams Beuren; Williams-Beureni sündroom; WS; Williamsi-Beureni sündroom; WBS; Лицо эльфа; Синдром лица эльфа; Вильямса синдром; Синдром Уильямса; Fanconi-Schlesiner-Syndrom; Idiopathische Hyperkalzämie; Williams-Syndrom; Williams Syndrom; Elfin-face-Syndrom; Viljamso Beureno sindromas; Viljamso beureno; Fanconi-Schlesingerjev sindrom; monosomija 7q11.23; Williams syndrome; Zespół Williamsa i Beurena; Zespół Williamsa-Beurena; תסמונת וויליאמס; Williams-syndroom; Williams-Beuren-Syndroom; Williams-Beurensyndroom; Williamssyndroom; Williamssyndrooom; Williams-Beuren syndroom; Williams syndroom; Вільямса синдром; Sindrome de Williams; Sindrome de Williams Beuren; Síndrome de Williams-Beuren; Síndrome de Williams Beuren; Sindrome de Williams-Beuren; Williamsin syndrooma; Williams-Beurenin oireyhtymä; Williams-Beurenin syndrooma; 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; Williams syndrome; sindromo de Williams-Beuren; σύνδρομο Williams; வில்லியம் நோய்க்கூட்டறிகுறி</nowiki>