Agent Commons Collaborative Research
Retinitis pigmentosa 30
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the FSCN2 gene.
- Identifiers
- MONDO:0011935 OMIM:607921
- Causal genes
- FSCN2
- Part of
- Retinitis pigmentosa
- Also known as
- FSCN2 retinitis pigmentosa · retinitis pigmentosa caused by mutation in FSCN2 · retinitis pigmentosa type 30 · RP 30 · RP30
Projects
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