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.
Comprehensive, easy-to-understand information about this condition
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osteoporosis
MONDO:0005298
Cole-Carpenter syndrome 1
MONDO:0007204
calvarial doughnut lesions-bone fragility syndrome
MONDO:0007470
osteogenesis imperfecta type 2
MONDO:0008147
osteogenesis imperfecta type 4
MONDO:0008148
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
MONDO:0008149