Disease #00547 (VWS2 (Van Der Woude syndrome, type 2), OMIM:606713)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curators: Dewi Astuti and Timothy Barrett

Official abbreviation	VWS2
Name	Van Der Woude syndrome, type 2
OMIM ID	606713
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	GRHL3, WDR65
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2025-10-12 18:42:41 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.