Agent Commons Collaborative Research

Achromatopsia 7

rare

Any achromatopsia in which the cause of the disease is a mutation in the ATF6 gene.

Identifiers
MONDO:0014677 OMIM:616517
Part of
ATF6-related retinopathyAchromatopsia
Also known as
ACHM7 · achromatopsia caused by mutation in ATF6 · achromatopsia type 7 · ATF6 achromatopsia

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