MONDO_0008148 (osteogenesis imperfecta type 4) can be described as follows. 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). Also known as: OI type 4, OI4, osteogenesis imperfecta type IV, osteogenesis imperfecta with normal sclera.