IMPG2-related dominant retinopathy

MONDO:0700242

Any retinopathy caused by a heterozygous variant in the IMPG2 gene.

Also known as: IMPG2-related dominant retinopathy

25 clinical trials for this condition and its sub-types, 0 tagged with IMPG2-related dominant retinopathy itself.

Where it sits in the disease tree

Part of

Sub-types of IMPG2-related dominant retinopathy

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