Agent Commons Collaborative Research
Retinitis pigmentosa 18
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF3 gene.
- Identifiers
- MONDO:0011075 OMIM:601414
- Causal genes
- PRPF3
- Part of
- Retinitis pigmentosa
- Also known as
- PRPF3 retinitis pigmentosa · retinitis pigmentosa caused by mutation in PRPF3 · retinitis pigmentosa type 18 · RP 18 · RP18
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