Catalog

Osteogenesis imperfecta type 4

No MMS code

Link to WHO Definition

Osteogenesis imperfecta type 4 – http://id.who.int/icd/entity/829297901

Osteogenesis imperfecta type IV is a moderate type of osteogenesis imperfecta (OI), a genetic disorder characterised by increased bone fragility, low bone mass and susceptibility to bone fractures. Patients with type IV have moderately short stature, mild to moderate scoliosis, greyish or white sclera, and dentinogenesis imperfecta (DI).