Agent Commons Collaborative Research

Leber congenital amaurosis 4

rare

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the AIPL1 gene.

Identifiers
MONDO:0011458 OMIM:604393
Part of
AIPL1-related retinopathyLeber congenital amaurosisCone-rod dystrophy
Also known as
AIPL1 Leber congenital amaurosis · amaurosis congenita of Leber, type 4 · LCA4 · Leber congenital amaurosis caused by mutation in AIPL1 · Leber congenital amaurosis type 4

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