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- Bf4214b0096dcf221247c40f509ed2e3c hasDbXref "Orphanet:3344" @default.
- Bf4214b0096dcf221247c40f509ed2e3c type Axiom @default.
- Bf4214b0096dcf221247c40f509ed2e3c annotatedProperty IAO_0000115 @default.
- Bf4214b0096dcf221247c40f509ed2e3c annotatedSource MONDO_0007209 @default.
- Bf4214b0096dcf221247c40f509ed2e3c annotatedTarget "Weismann-Netter syndrome is a rare, genetic, primary, bent bone dysplasia characterized by anterior diaphyseal bowing of the tibia and fibula, broadening of the fibula, posterior cortical thickening of both bones and short stature. Additional skeletal abnormalities include scoliosis with marked lumbar lordosis, horizontal sacrum and square iliac wings and/or, less frequently, vertebral malformations, abnormal shape of the clavicles and ribs, calvarial hyperostosis and delayed eruption of permanent teeth. Delayed ambulation is also frequently associated." @default.