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- B1ff1de3fe0b2223cc58418d54ca4f30e hasDbXref "Orphanet:216828" @default.
- B1ff1de3fe0b2223cc58418d54ca4f30e type Axiom @default.
- B1ff1de3fe0b2223cc58418d54ca4f30e annotatedProperty IAO_0000115 @default.
- B1ff1de3fe0b2223cc58418d54ca4f30e annotatedSource MONDO_0012591 @default.
- B1ff1de3fe0b2223cc58418d54ca4f30e annotatedTarget "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)." @default.