ATF6-related retinopathy

MONDO:0100447

A retinopathy caused by biallelic variants in the AFT6 gene.

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

26 clinical trials for this condition and its sub-types, 0 tagged with ATF6-related retinopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inherited retinal dystrophy (513)

Sub-types of ATF6-related retinopathy

Achromatopsia 7 1 trial

Including sub-types (26) Tagged with ATF6-related retinopathy (0)

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