Achromatopsia 7

MONDO:0014677

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

Also known as: ACHM7, ATF6 achromatopsia, achromatopsia 7, achromatopsia caused by mutation in ATF6, achromatopsia type 7

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

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