Autosomal dominant Robinow syndrome 3

Definition

Any Robinow syndrome in which the cause of the disease is a mutation in the DVL3 gene.

Also known as autosomal dominant Robinow syndrome type 3, DRS3, DVL3 Robinow syndrome, Robinow syndrome caused by mutation in DVL3, Robinow syndrome, autosomal dominant 3, Robinow syndrome, autosomal dominant type 3 — per MONDO

Also identified as

• DOID 0060767 per MONDO
• OMIM 616894 per MONDO
• UMLS C4225164 per MONDO