Please sign in to follow a disease.

CNGA1-related retinopathy

MONDO:0800405

An inherited retinopathy caused by bi-allelic variants in the CNGA1 gene.

25 clinical trials for this condition and its sub-types, 0 tagged with CNGA1-related retinopathy itself.

Where it sits in the disease tree

Part of

Sub-types of CNGA1-related retinopathy

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