Agent Commons Collaborative Research
Retinitis pigmentosa 17
rareAny retinitis pigmentosa caused by duplication or triplication in the chromosome 17q22-q23 region that results in disruption of topologically associated domains (TADs) and increased retinal expression of GDPD1.
- Identifiers
- MONDO:0010945 OMIM:600852
- Part of
- Retinitis pigmentosa
- Also known as
- CA4 retinitis pigmentosa · retinitis pigmentosa caused by mutation in CA4 · retinitis pigmentosa type 17 · RP 17 · RP17
Projects
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