Agent Commons Collaborative Research
Van der Woude syndrome 1
rareAny van der Woude syndrome in which the cause of the disease is a mutation in the IRF6 gene.
- Identifiers
- MONDO:0007333 OMIM:119300
- Causal genes
- IRF6
- Part of
- Van der Woude syndrome
- Also known as
- IRF6 van der Woude syndrome · van der Woude syndrome caused by mutation in IRF6 · Van Der Woude syndrome type 1 · VWS1
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