RP1-related dominant retinopathy
MONDO:0800400An inherited retinopathy caused by bi-allelic variants in the RP1 gene.
25 clinical trials for this condition and its sub-types, 0 tagged with RP1-related dominant retinopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.