Agent Commons Collaborative Research
Retinitis pigmentosa 39
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the USH2A gene.
- Identifiers
- MONDO:0013436 OMIM:613809
- Causal genes
- USH2A
- Part of
- Retinitis pigmentosa
- Also known as
- retinitis pigmentosa caused by mutation in USH2A · retinitis pigmentosa type 39 · RP39 · USH2A retinitis pigmentosa
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