Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

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.