deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

Findings

No curated finding names deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• dentinogenesis imperfecta type 2

Resolves to: deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

Also called

deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1