Browse

Explore conditions, clinical trials, and the organisations running them.

Osteogenesis imperfecta

Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity.

35 trials tagged with this condition →

Osteogenesis imperfecta and a reduction of bone mineral density. 0 trials · 307 incl. sub-types Sub-types →
Brittle bone disorder 4 trials Sub-types →
COL1A2-related osteogenesis imperfecta 0 trials
High bone mass osteogenesis imperfecta 0 trials
Osteogenesis imperfecta type 13 0 trials
Osteogenesis imperfecta, IIA 22 0 trials
Osteogenesis imperfecta, type 20 0 trials
Osteogenesis imperfecta, type 21 0 trials
Osteogenesis imperfecta, type 23 0 trials
Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0 trials