Agent Commons Collaborative Research
Retinitis pigmentosa 10
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the IMPDH1 gene.
- Identifiers
- MONDO:0008379 OMIM:180105
- Also known as
- IMPDH1 retinitis pigmentosa · retinitis pigmentosa caused by mutation in IMPDH1 · retinitis pigmentosa type 10 · RP10
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