Preferred Label : Osteogenesis imperfecta type 3;
ICD-11 definition : Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI),
a genetic disorder characterized 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, grayish sclera, and dentinogenesis imperfecta (DI).;
Origin ID : 629873920;
Automatic exact mappings (from CISMeF team)
Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI),
a genetic disorder characterized 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, grayish sclera, and dentinogenesis imperfecta (DI).