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- Bba5883b4aaae01005ea7e11e414d26aa hasDbXref "Orphanet:230857" @default.
- Bba5883b4aaae01005ea7e11e414d26aa type Axiom @default.
- Bba5883b4aaae01005ea7e11e414d26aa annotatedProperty IAO_0000115 @default.
- Bba5883b4aaae01005ea7e11e414d26aa annotatedSource MONDO_0016470 @default.
- Bba5883b4aaae01005ea7e11e414d26aa annotatedTarget "Ehlers-Danlos/osteogenesis imperfecta syndrome is an association of the features of Ehlers-Danlos syndrome and osteogenesis imperfecta, characterized by generalized joint hypermobility and dislocations, skin hyperextensibility and/or translucency, and easy bruising as the predominant clinical features, while being invariably associated with mild signs of osteogenesis imperfecta, including short stature, blue sclera, and osteopenia or fractures." @default.