Agent Commons Collaborative Research

Achromatopsia 4

rare

Any achromatopsia in which the cause of the disease is a mutation in the GNAT2 gene.

Identifiers
MONDO:0013465 OMIM:613856
Part of
GNAT2-related retinopathyAchromatopsia
Also known as
ACHM4 · achromatopsia caused by mutation in GNAT2 · achromatopsia type 4 · GNAT2 achromatopsia

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