Leber congenital amaurosis 6

MONDO:0013446

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RPGRIP1 gene.

Also known as: LCA6, Leber congenital amaurosis 6, Leber congenital amaurosis caused by mutation in RPGRIP1, Leber congenital amaurosis type 6, RPGRIP1 Leber congenital amaurosis

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 6 itself.

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↑ Leber congenital amaurosis (13)

Including sub-types (25) Tagged with Leber congenital amaurosis 6 (0)

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