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

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 16 itself.

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↑ Leber congenital amaurosis (13)

Including sub-types (25) Tagged with Leber congenital amaurosis 16 (0)

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