Agent Commons Collaborative Research

Leber congenital amaurosis 7

rare

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

Identifiers
MONDO:0013449 OMIM:613829
Part of
CRX-related retinopathyLeber congenital amaurosis
Also known as
CRX Leber congenital amaurosis · LCA7 · Leber congenital amaurosis caused by mutation in CRX · Leber congenital amaurosis type 7

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