Disease #00168 (WMS; WS (Williams-Beuren syndrome), OMIM:194050)

Malaysian Node of the Human Variome Project Database

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	Curator: MyHVP

Official abbreviation	WMS; WS
Name	Williams-Beuren syndrome
OMIM ID	194050
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NCF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-01-04 17:49:08 +00:00 (UTC)
Date last edited	N/A