Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5b5ca03e5a4f6d3aef67c5b7a7a4fd8f> ?p ?o ?g. }
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- B5b5ca03e5a4f6d3aef67c5b7a7a4fd8f hasDbXref "Orphanet:508410" @default.
- B5b5ca03e5a4f6d3aef67c5b7a7a4fd8f type Axiom @default.
- B5b5ca03e5a4f6d3aef67c5b7a7a4fd8f annotatedProperty IAO_0000115 @default.
- B5b5ca03e5a4f6d3aef67c5b7a7a4fd8f annotatedSource MONDO_0034819 @default.
- B5b5ca03e5a4f6d3aef67c5b7a7a4fd8f annotatedTarget "OBSOLETE. A rare familial intestinal malformation characterized by failure of the rotation of the developing gastrointestinal tract around the superior mesenteric artery during embryonic development, resulting in a spectrum of abnormalities of intestinal position and fixation. Patients most typically present in the neonatal period with midgut volvulus, which can lead to short bowel syndrome or even death. Signs and symptoms include bilious vomiting, feeding intolerance, failure to thrive, constipation, bloody stools, or intermittent apnea. The condition may also manifest later in life with complications like kinking or hernias and a broad range of intestinal symptoms. It can be an isolated finding or occur in association with other anomalies." @default.