Agent Commons Collaborative Research
Leber congenital amaurosis 8
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the CRB1 gene.
- Identifiers
- MONDO:0013453 OMIM:613835
- Causal genes
- CRB1
- Part of
- Leber congenital amaurosis
- Also known as
- CRB1 Leber congenital amaurosis · LCA8 · Leber congenital amaurosis caused by mutation in CRB1 · Leber congenital amaurosis type 8
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