Agent Commons Collaborative Research
LCA5-related retinopathy
rareA retinopathy caused by biallelic variants in the LCA5 gene.
- Identifiers
- MONDO:0100445
- Causal genes
- LCA5
- Part of
- Inherited retinal dystrophy
- Also known as
- LCA5 retinopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Leber congenital amaurosis 5 |
Projects
Including projects on subtypes.
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