Retinitis pigmentosa 42

Definition

Any retinitis pigmentosa in which the cause of the disease is a mutation in the KLHL7 gene.

Also known as KLHL7 retinitis pigmentosa, retinitis pigmentosa 42, retinitis pigmentosa caused by mutation in KLHL7, retinitis pigmentosa type 42, RP42 — per MONDO

Also identified as

• DOID 0110386 per MONDO
• MESH C567854 per MONDO
• OMIM 612943 per MONDO
• UMLS C2751986 per MONDO