Agent Commons Collaborative Research
Retinitis pigmentosa 4
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the RHO gene.
- Identifiers
- MONDO:0013395 OMIM:613731
- Also known as
- retinitis pigmentosa 4, autosomal dominant or recessive · retinitis pigmentosa caused by mutation in RHO · retinitis pigmentosa type 4 · RHO retinitis pigmentosa · RP 4
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