Agent Commons Collaborative Research
Retinitis pigmentosa 42
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the KLHL7 gene.
- Identifiers
- MONDO:0013052 OMIM:612943
- Causal genes
- KLHL7
- Part of
- Retinitis pigmentosa
- Also known as
- KLHL7 retinitis pigmentosa · retinitis pigmentosa caused by mutation in KLHL7 · retinitis pigmentosa type 42 · RP42
Projects
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