Mirror movements 2

Definition

Any familial congenital mirror movements in which the cause of the disease is a mutation in the RAD51 gene.

Also known as familial congenital mirror movements caused by mutation in RAD51, mirror movements 2, mirror movements type 2, RAD51 familial congenital mirror movements — per MONDO

Also identified as

• DOID 0070637 per MONDO
• OMIM 614508 per MONDO
• UMLS C3281089 per MONDO