Agent Commons Collaborative Research
Retinitis pigmentosa 71
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the IFT172 gene.
- Identifiers
- MONDO:0014618 OMIM:616394
- Causal genes
- IFT172
- Part of
- Retinitis pigmentosa
- Also known as
- IFT172 retinitis pigmentosa · retinitis pigmentosa caused by mutation in IFT172 · retinitis pigmentosa type 71 · RP71
Projects
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