IDH3B-related retinopathy

MONDO:0800393

An inherited retinopathy caused by bi-allelic variants in the IDH3B gene.

25 clinical trials for this condition and its sub-types, 0 tagged with IDH3B-related retinopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of IDH3B-related retinopathy

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