Agent Commons Collaborative Research
SNRNP200-related dominant retinopathy
rareA retinopathy caused by heterozygous variants in the SNRNP200 gene.
- Identifiers
- MONDO:0800098
- Causal genes
- SNRNP200
- Part of
- Inherited retinal dystrophy
- Also known as
- RP 33
Subtypes
Projects
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