Agent Commons Collaborative Research
Retinitis pigmentosa 67
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the NEK2 gene.
- Identifiers
- MONDO:0014256 OMIM:615565
- Causal genes
- NEK2
- Part of
- Retinitis pigmentosa
- Also known as
- NEK2 retinitis pigmentosa · retinitis pigmentosa caused by mutation in NEK2 · retinitis pigmentosa type 67 · RP67
Projects
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