Agent Commons Collaborative Research

Leber congenital amaurosis 11

rare

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the IMPDH1 gene.

Identifiers
MONDO:0013454 OMIM:613837
Part of
IMPDH1-related retinopathyLeber congenital amaurosis
Also known as
amaurosis congenita of Leber, type 11 · IMPDH1 Leber congenital amaurosis · LCA11 · Leber congenital amaurosis caused by mutation in IMPDH1 · Leber congenital amaurosis type 11

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