Retinitis pigmentosa 39

Definition

Any retinitis pigmentosa in which the cause of the disease is a mutation in the USH2A gene.

Also known as retinitis pigmentosa 39, retinitis pigmentosa caused by mutation in USH2A, retinitis pigmentosa type 39, RP39, USH2A retinitis pigmentosa — per MONDO

Also identified as

• DOID 0110360 per MONDO
• OMIM 613809 per MONDO
• UMLS C3151138 per MONDO