Osteogenesis imperfecta type 5

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, OI type V, OI with calcification in interosseous membranes, OI, type 5, osteogenesis imperfecta, type 5

1 clinical trial for this condition and its sub-types, 1 tagged with Osteogenesis imperfecta type 5 itself.