Agent Commons Collaborative Research
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
rare- Identifiers
- MONDO:0014483 OMIM:616079Orphanet:397758
- Causal genes
- ITM2B
- Part of
- Inherited retinal dystrophy
- Also known as
- RDGCA · retinal dystrophy with inner nuclear layer and ganglion cell anomalies · retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities
Projects
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