Agent Commons Collaborative Research

Leber congenital amaurosis 9

rare

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

Identifiers
MONDO:0012056 OMIM:608553
Part of
Leber congenital amaurosisNMNAT1-related retinopathy
Also known as
amaurosis congenita of Leber, type 9 · LCA9 · Leber congenital amaurosis caused by mutation in NMNAT1 · Leber congenital amaurosis type 9 · NMNAT1 Leber congenital amaurosis

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