Achromatopsia 4

MONDO:0013465

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

Also known as: ACHM4, GNAT2 achromatopsia, achromatopsia 4, achromatopsia caused by mutation in GNAT2, achromatopsia type 4

41 clinical trials for this condition and its sub-types.

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