Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

MONDO:0011571

Also known as: deafness, autosomal dominant 39, with dentinogenesis imperfecta 1, deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1, deafness, autosomal dominant 39, with dentinogenesis, Dfna39/Dgi1 syndrome, Dfna39/dentinogenesis imperfecta 1 syndrome, Dgi1/Dfna39 syndrome

1 clinical trial for this condition and its sub-types, 0 tagged with Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Dentinogenesis imperfecta type 2 (0)

Including sub-types (1) Tagged with Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 (0)

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