osteogenesis imperfecta type 5 (Monarch Disease Ontology identifier MONDO_0012591) can be described as follows. Osteogenesis imperfecta type V is a moderate type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures with variable severity. OI type V is characterized by mild to moderate short stature, dislocation of the radial head, mineralized interosseous membranes, hyperplasic callus, white sclera and no dentinogenesis imperfecta (DI). Also known as: IFITM5 osteogenesis imperfecta, OI type 5, OI5, osteogenesis imperfecta caused by mutation in IFITM5, osteogenesis imperfecta type V.