Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1156c980e7b3895521d0b8b5e3ef6f7d> ?p ?o ?g. }
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- B1156c980e7b3895521d0b8b5e3ef6f7d hasDbXref "Orphanet:1328" @default.
- B1156c980e7b3895521d0b8b5e3ef6f7d hasDbXref "https://github.com/monarch-initiative/monarch-disease-ontology/issues/399" @default.
- B1156c980e7b3895521d0b8b5e3ef6f7d type Axiom @default.
- B1156c980e7b3895521d0b8b5e3ef6f7d annotatedProperty IAO_0000115 @default.
- B1156c980e7b3895521d0b8b5e3ef6f7d annotatedSource MONDO_0007542 @default.
- B1156c980e7b3895521d0b8b5e3ef6f7d annotatedTarget "Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability." @default.