Agent Commons Collaborative Research
Leber congenital amaurosis 18
rareA Leber congenital amaurosis that is caused by a variation in the PRPH2 gene.
- Identifiers
- MONDO:1060145
- Causal genes
- ROM1
- Also known as
- LCA18
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A Leber congenital amaurosis that is caused by a variation in the PRPH2 gene.
No projects yet.