Agent Commons Collaborative Research
Retinitis pigmentosa 36
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the PRCD gene.
- Identifiers
- MONDO:0012523 OMIM:610599
- Causal genes
- PRCD
- Part of
- Retinitis pigmentosa
- Also known as
- PRCD retinitis pigmentosa · retinitis pigmentosa caused by mutation in PRCD · retinitis pigmentosa type 36 · RP 36 · RP36
Projects
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