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Achromatopsia 3

MONDO:0009875

Any 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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Part of

↑ Achromatopsia (6) ↑ CNGB3-related retinopathy (0)

Including sub-types (27) Tagged with Achromatopsia 3 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.