ONKI3 | Medical Subject Headings

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Waardenburg's Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Waardenburg's Syndrome 32 coordinate concepts ∟ Alagille Syndrome \| ∟ Angelman Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Bloom Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Cockayne Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Holoprosencephaly \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Rubinstein-Taybi Syndrome \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Waardenburg's Syndrome Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) X
Annotation:	a syndrome of multiple abnorm; check syndrome book for other Waardenburg skull deform syndromes; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	91(66); was see under ABNORMALITIES, MULTIPLE 1975-90 X
publicMeSHNote*:	91; was see under ABNORMALITIES, MULTIPLE 1975-90 X
Scope note:	Rare, autosomal dominant disease with variable penetrance and several known clinical types. Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities. X
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1991-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Alagille Syndrome \| Angelman Syndrome \| Bardet-Biedl Syndrome \| Basal Cell Nevus Syndrome \| Beckwith-Wiedemann Syndrome \| Bloom Syndrome \| Branchio-Oto-Renal Syndrome \| Cockayne Syndrome \| Cri-du-Chat Syndrome \| De Lange Syndrome \| Down Syndrome \| Ectodermal Dysplasia \| Gardner Syndrome \| Holoprosencephaly \| Incontinentia Pigmenti \| Laurence-Moon Syndrome \| LEOPARD Syndrome \| Marfan Syndrome \| Mobius Syndrome \| Nail-Patella Syndrome \| Oculocerebrorenal Syndrome \| Orofaciodigital Syndromes \| POEMS Syndrome \| Prader-Willi Syndrome \| Proteus Syndrome \| Prune Belly Syndrome \| Rubella Syndrome, Congenital \| Rubinstein-Taybi Syndrome \| Short Rib-Polydactyly Syndrome \| Smith-Lemli-Opitz Syndrome \| Wolfram Syndrome \| Zellweger Syndrome X
URI:	X
Labels and equivalent concepts:	Waardenburgin oireyhtymä (fi) Waardenburgin syndrooma (fi, replaced) Waardenburgs syndrom (sv) Waardenburg-Klein Syndrome (en, replaced) Klein-Waardenburg Syndrome (en, replaced) Syndroma Waardenburg (la-FI, replaced) X
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