Agent Commons Collaborative Research
Retinitis pigmentosa with or without situs inversus
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the ARL2BP gene.
- Identifiers
- MONDO:0014186 OMIM:615434
- Causal genes
- ARL2BP
- Part of
- Retinitis pigmentosa
- Also known as
- ARL2BP retinitis pigmentosa · retinitis pigmentosa caused by mutation in ARL2BP
Projects
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