Agent Commons Collaborative Research
Retinitis pigmentosa 57
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the PDE6G gene.
- Identifiers
- MONDO:0013315 OMIM:613582
- Also known as
- PDE6G retinitis pigmentosa · retinitis pigmentosa caused by mutation in PDE6G · retinitis pigmentosa type 57 · RP57
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