Osteogenesis imperfecta type 1

Osteogenesis imperfecta type I is a mild type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures.

Also known as: Adair-Dighton syndrome, COL1A1-related osteogenesis imperfecta, OI type 1, OI1, Van der Hoeve syndrome, mild osteogenesis imperfecta, non-deforming osteogenesis imperfecta, osteogenesis imperfecta type 1

43 clinical trials for this condition and its sub-types.