Catalog

Osteogenesis imperfecta type 3

No MMS code

Link to WHO Definition

Osteogenesis imperfecta type 3 – http://id.who.int/icd/entity/629873920

Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI), a genetic disorder characterised by increased bone fragility, low bone mass and susceptibility to bone fractures. The main signs of type III include very short stature, a triangular face, severe scoliosis, greyish sclera, and dentinogenesis imperfecta (DI).