Agent Commons Collaborative Research
Retinitis pigmentosa 13
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF8 gene.
- Identifiers
- MONDO:0010806 OMIM:600059
- Also known as
- PRPF8 retinitis pigmentosa · retinitis pigmentosa caused by mutation in PRPF8 · retinitis pigmentosa type 13 · RP 13 · RP13
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