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van der Woude syndrome 2

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Any van der Woude syndrome in which the cause of the disease is a mutation in the GRHL3 gene.
Uniprot Description An autosomal dominant developmental disorder characterized by lower lip pits, cleft lip and/or cleft palate.
Mondo Term and Equivalent IDs
MONDO:0011712:  van der Woude syndrome 2
GARD:0007846: 
MESH:C536529: 
UMLS:C1847604: