Leber congenital amaurosis 17

MONDO:0014145

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the GDF6 gene.

Also known as: GDF6 Leber congenital amaurosis, LCA17, Leber congenital amaurosis 17, Leber congenital amaurosis caused by mutation in GDF6, Leber congenital amaurosis type 17

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 17 itself.

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↑ Leber congenital amaurosis (13)

Including sub-types (25) Tagged with Leber congenital amaurosis 17 (0)

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