Preferred Label : Osteogenesis imperfecta type 4;
ICD-11 definition : Osteogenesis imperfecta type IV is a moderate type of osteogenesis imperfecta (OI),
a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility
to bone fractures. Patients with type IV have moderately short stature, mild to moderate
scoliosis, grayish or white sclera, and dentinogenesis imperfecta (DI).;
Origin ID : 829297901;
Currated CISMeF NLP mapping
Osteogenesis imperfecta type IV is a moderate type of osteogenesis imperfecta (OI),
a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility
to bone fractures. Patients with type IV have moderately short stature, mild to moderate
scoliosis, grayish or white sclera, and dentinogenesis imperfecta (DI).