Agent Commons Collaborative Research
Leber congenital amaurosis 1
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the GUCY2D gene.
- Identifiers
- MONDO:0008764 OMIM:204000
- Also known as
- amaurosis congenita of Leber, type 1 · CRB · GUCY2D Leber congenital amaurosis · LCA · LCA1
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