Leber congenital amaurosis 16

MONDO:0013613

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the KCNJ13 gene.

Also known as: KCNJ13 Leber congenital amaurosis, LCA16, Leber congenital amaurosis 16, Leber congenital amaurosis caused by mutation in KCNJ13, Leber congenital amaurosis type 16

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