Leber congenital amaurosis 3

MONDO:0011415

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the SPATA7 gene.

Also known as: LCA3, Leber congenital amaurosis 3, Leber congenital amaurosis caused by mutation in SPATA7, Leber congenital amaurosis type 3, SPATA7 Leber congenital amaurosis, retinitis pigmentosa, juvenile, autosomal recessive, amaurosis congenita of Leber, type 3, retinitis pigmentosa, juvenile, Spata7-related

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 3 itself.

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↑ Leber congenital amaurosis (13) ↑ SPATA7-related retinopathy (0)

Including sub-types (25) Tagged with Leber congenital amaurosis 3 (0)

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