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- B3353579a9ba5cc280f8e7ac92b6c05e1 hasDbXref "Orphanet:3344" @default.
- B3353579a9ba5cc280f8e7ac92b6c05e1 type Axiom @default.
- B3353579a9ba5cc280f8e7ac92b6c05e1 annotatedProperty IAO_0000115 @default.
- B3353579a9ba5cc280f8e7ac92b6c05e1 annotatedSource MONDO_0007209 @default.
- B3353579a9ba5cc280f8e7ac92b6c05e1 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.