Leber congenital amaurosis 9

MONDO:0012056

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the NMNAT1 gene.

Also known as: LCA9, Leber congenital amaurosis 9, Leber congenital amaurosis caused by mutation in NMNAT1, Leber congenital amaurosis type 9, NMNAT1 Leber congenital amaurosis, amaurosis congenita of Leber, type 9

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 9 itself.

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↑ Leber congenital amaurosis (12) ↑ NMNAT1-related retinopathy (0)

Including sub-types (25) Tagged with Leber congenital amaurosis 9 (0)

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