Cone-rod dystrophy 13

Definition

Any cone-rod dystrophy in which the cause of the disease is a mutation in the RPGRIP1 gene.

Also known as cone-rod dystrophy 13, cone-rod dystrophy caused by mutation in RPGRIP1, cone-rod dystrophy type 13, CORD13, RPGRIP1 cone-rod dystrophy — per MONDO

Also identified as

• DOID 0111016 per MONDO
• MESH C567698 per MONDO
• OMIM 608194 per MONDO
• UMLS C2750720 per MONDO