Details of Disease

General Information of Disease (ID: DIS4G3U8)

Disease Name Van der Woude syndrome 2
Synonyms VAN DER Woude syndrome 2; VWS2; van der Woude syndrome 2; GRHL3 van der Woude syndrome; Van Der Woude syndrome type 2; van der Woude syndrome caused by mutation in GRHL3
Definition Any van der Woude syndrome in which the cause of the disease is a mutation in the GRHL3 gene.
Disease Hierarchy
DISYKSRF: Genetic disease
DISADZS1: Van der Woude syndrome
DIS4G3U8: Van der Woude syndrome 2
Disease Identifiers
MONDO ID
MONDO_0011712
MESH ID
C536529
UMLS CUI
C1847604
OMIM ID
606713
MedGen ID
338272

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
GRHL3 OT1V4ZEH Strong Autosomal dominant [1]
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References

1 The functions of grainy head-like proteins in animals and fungi and the evolution of apical extracellular barriers. PLoS One. 2012;7(5):e36254. doi: 10.1371/journal.pone.0036254. Epub 2012 May 9.