Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

IMPG1-related dominant retinopathy

MONDO:1040036

Any retinopathy caused by an autosomal dominant variant in the IMPG1 gene.

Also known as: IMPG1-related dominant retinopathy

25 clinical trials for this condition and its sub-types, 0 tagged with IMPG1-related dominant retinopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of IMPG1-related dominant retinopathy

Sort by