Disease Summary help help Associated Targets (2)Tbio1Tdark1 Explore Associated Targets list 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 OMIM:119300: VAN DER WOUDE SYNDROME 1open_in_new