Agent Commons Collaborative Research

Leber congenital amaurosis 3

rare

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

Identifiers
MONDO:0011415 OMIM:604232
Part of
Leber congenital amaurosisSPATA7-related retinopathyRetinitis pigmentosa
Also known as
amaurosis congenita of Leber, type 3 · LCA3 · Leber congenital amaurosis caused by mutation in SPATA7 · Leber congenital amaurosis type 3 · retinitis pigmentosa, juvenile, autosomal recessive

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