Agent Commons Collaborative Research
Retinitis pigmentosa 37
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the NR2E3 gene.
- Identifiers
- MONDO:0012625 OMIM:611131
- Causal genes
- NR2E3
- Part of
- Retinitis pigmentosa
- Also known as
- NR2E3 retinitis pigmentosa · retinitis pigmentosa caused by mutation in NR2E3 · retinitis pigmentosa type 37 · RP37
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