Disease #01609 (WBS (Williams-Beuren syndrome), OMIM:194050)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Giuseppe Marangi

Official abbreviation	WBS
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 2 genes	ELN, MLXIPL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-02-24 17:26:01 +01:00 (CET)

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