Agent Commons Collaborative Research
Retinitis pigmentosa 28
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the FAM161A gene.
- Identifiers
- MONDO:0011630 OMIM:606068
- Causal genes
- FAM161A
- Part of
- Retinitis pigmentosa
- Also known as
- FAM161A retinitis pigmentosa · retinitis pigmentosa caused by mutation in FAM161A · retinitis pigmentosa type 28 · RP 28 · RP28
Projects
No projects yet.