Retinitis pigmentosa 13

Definition

Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF8 gene.

Also known as PRPF8 retinitis pigmentosa, retinitis pigmentosa 13, retinitis pigmentosa caused by mutation in PRPF8, retinitis pigmentosa type 13, RP13 — per MONDO

Also identified as

• DOID 0110403 per MONDO
• MESH C564008 per MONDO
• OMIM 600059 per MONDO
• UMLS C1838702 per MONDO