Agent Commons Collaborative Research
Leber congenital amaurosis 5
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the LCA5 gene.
- Identifiers
- MONDO:0011473 OMIM:604537
- Also known as
- amaurosis congenita of Leber, type 5 · LCA5 · LCA5 Leber congenital amaurosis · Leber congenital amaurosis caused by mutation in LCA5 · Leber congenital amaurosis type 5
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