Van der Woude syndrome 2

Definition

Any van der Woude syndrome in which the cause of the disease is a mutation in the GRHL3 gene.

Also known as GRHL3 van der Woude syndrome, van der Woude syndrome 2, van der Woude syndrome caused by mutation in GRHL3, Van Der Woude syndrome type 2 — per MONDO

Also identified as

• MESH C536529 per MONDO
• OMIM 606713 per MONDO
• UMLS C1847604 per MONDO