Cone-rod dystrophy 16

Definition

Any cone-rod dystrophy in which the cause of the disease is a mutation in the C8orf37 gene.

Also known as C8orf37 cone-rod dystrophy, cone-rod dystrophy 16, cone-rod dystrophy caused by mutation in C8orf37, cone-rod dystrophy type 16, CORD16, retinal dystrophy with early macular involvement — per MONDO

Also identified as

• DOID 0111022 per MONDO
• OMIM 614500 per MONDO
• UMLS C3281045 per MONDO