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Achromatopsia 3
MONDO:0009875Any achromatopsia in which the cause of the disease is a mutation in the CNGB3 gene.
Also known as: ACHM3, CNGB3 achromatopsia, achromatopsia 3, achromatopsia caused by mutation in CNGB3, achromatopsia type 3, ACHM1 (formerly), ACHM1, formerly, RMCH1 (formerly)
27 clinical trials for this condition and its sub-types, 0 tagged with Achromatopsia 3 itself.
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