Agent Commons Collaborative Research
Retinitis pigmentosa 32
rareA retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3.
- Identifiers
- MONDO:0012363 OMIM:609913
- Causal genes
- CLCC1
- Part of
- Retinitis pigmentosa
- Also known as
- retinitis pigmentosa type 32 · RP32
Projects
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