Agent Commons Collaborative Research
Leber congenital amaurosis 16
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the KCNJ13 gene.
- Identifiers
- MONDO:0013613 OMIM:614186
- Causal genes
- KCNJ13
- Part of
- Leber congenital amaurosis
- Also known as
- KCNJ13 Leber congenital amaurosis · LCA16 · Leber congenital amaurosis caused by mutation in KCNJ13 · Leber congenital amaurosis type 16
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