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van der Woude syndrome 1

Disease Summary
Associated Targets (2)
Tbio

1

Tdark

1


Mondo Description Any van der Woude syndrome in which the cause of the disease is a mutation in the IRF6 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:0007333:  van der Woude syndrome 1