Leber congenital amaurosis 8

MONDO:0013453

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CRB1 gene.

Also known as: CRB1 Leber congenital amaurosis, LCA8, Leber congenital amaurosis 8, Leber congenital amaurosis caused by mutation in CRB1, Leber congenital amaurosis type 8

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 8 itself.

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↑ Leber congenital amaurosis (13)

Including sub-types (25) Tagged with Leber congenital amaurosis 8 (0)

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