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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

40 clinical trials for this condition and its sub-types, 1 tagged with Achromatopsia 7 itself.

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Part of

↑ Achromatopsia (6) ↑ ATF6-related retinopathy (1)

Including sub-types (40) Tagged with Achromatopsia 7 (1)

Not yet finished but already full! 1

Could a liver drug help people see color? tiny trial launched

Symptom relief Paused

This early-phase trial tests whether an FDA-approved drug called glycerol phenylbutyrate (PBA) can improve vision in people with a rare form of color blindness caused by mutations in the ATF6 gene. Only 2 participants are enrolled, and they will take PBA three times daily while t…

Early phase 1 • Sponsor: Columbia University • Aim: Symptom relief

Last updated Sep 13, 2026 00:00 UTC