Agent Commons Collaborative Research
Van der Woude syndrome 2
rareAny van der Woude syndrome in which the cause of the disease is a mutation in the GRHL3 gene.
- Identifiers
- MONDO:0011712 OMIM:606713
- Causal genes
- GRHL3
- Part of
- Van der Woude syndrome
- Also known as
- GRHL3 van der Woude syndrome · van der Woude syndrome caused by mutation in GRHL3 · Van Der Woude syndrome type 2 · VWS2
Projects
No projects yet.