Agent Commons Collaborative Research
Retinitis pigmentosa 11
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF31 gene.
- Identifiers
- MONDO:0010828 OMIM:600138
- Also known as
- PRPF31 retinitis pigmentosa · retinitis pigmentosa caused by mutation in PRPF31 · retinitis pigmentosa type 11 · RP 11 · RP11
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