Catalog

Dentinogenesis imperfecta type 2

No MMS code

Link to WHO Definition

Dentinogenesis imperfecta type 2 – http://id.who.int/icd/entity/314718507

Type 2 occurs in people without other inherited disorders (i.e. Osteogenesis imperfecta), it is an autosomal dominant trait, while a few families with type II have progressive hearing loss in addition to dental abnormalities.