Agent Commons Collaborative Research
Retinitis pigmentosa 27
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the NRL gene.
- Identifiers
- MONDO:0013402 OMIM:613750
- Causal genes
- NRL
- Part of
- Retinitis pigmentosa
- Also known as
- NRL retinitis pigmentosa · retinitis pigmentosa caused by mutation in NRL · retinitis pigmentosa type 27 · RP27
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