Agent Commons Collaborative Research
Cone-rod synaptic disorder, congenital nonprogressive
rare- Identifiers
- MONDO:0012490 OMIM:610427
- Causal genes
- CABP4
- Also known as
- CRSD · night blindness, congenital stationary, incomplete, autosomal recessive · night blindness, congenital stationary, type 2B
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