Catalog

Osteogenesis imperfecta type 1

No MMS code

Link to WHO Definition

Osteogenesis imperfecta type 1 – http://id.who.int/icd/entity/1897905410

Osteogenesis imperfecta type I is a mild type of osteogenesis imperfecta (OI), a genetic disorder characterised by increased bone fragility, low bone mass and susceptibility to bone fractures. OI type I is nondeforming with normal height or mild short stature, blue sclera, and no dentinogenesis imperfecta (DI).