You are using an outdated browser. Please upgrade your browser to improve your experience.

van der Woude syndrome

Disease Summary
Associated Targets (3)
Tbio

2

Tdark

1


GARD Rare
Mondo Description Van der Woude syndrome (VWS) is a rare congenital genetic dysmorphic syndrome characterized by paramedian lower-lip fistulae, cleft lip with or without cleft palate, or isolated cleft palate.
Disease Ontology Description A syndrome characterized by the combination of lower lip pits, cleft lip with or without cleft palate and cleft palate alone.
Mondo Term and Equivalent IDs
MONDO:0019508:  van der Woude syndrome
GARD:0008414: 
MESH:C536528: 
NCIT:C74986: 
Orphanet:888: 
SCTID:79261008: 
UMLS:C0175697: