Agent Commons Collaborative Research
Retinitis pigmentosa 61
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the CLRN1 gene.
- Identifiers
- MONDO:0013610 OMIM:614180
- Causal genes
- CLRN1
- Part of
- Retinitis pigmentosa
- Also known as
- CLRN1 retinitis pigmentosa · retinitis pigmentosa caused by mutation in CLRN1 · retinitis pigmentosa type 61 · RP61
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