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- Ba1f1385d0abefeafb5aaeb2cc1ef9989 hasDbXref "Orphanet:1209" @default.
- Ba1f1385d0abefeafb5aaeb2cc1ef9989 type Axiom @default.
- Ba1f1385d0abefeafb5aaeb2cc1ef9989 annotatedProperty IAO_0000115 @default.
- Ba1f1385d0abefeafb5aaeb2cc1ef9989 annotatedSource MONDO_0011514 @default.
- Ba1f1385d0abefeafb5aaeb2cc1ef9989 annotatedTarget "Tricuspid atresia is (TA) a rare congenital heart malformation characterized by the congenital agenesis of tricuspid valve leading to severe hypoplasia of right ventricle (functionally univentricular). TA is associated with normally related or transposed great vessels (TGV), an obligatory interatrial connection that is crucial for survival (patent foramen ovale or atrial septal defect, osteum secondum type), ventricular septal defect (in 90% cases), pulmonary outflow obstruction - pulmonary atresia, stenosis or hypoplasia (usually in TA with normally related vessels but also in TGV), aortic coarctation and/or aortic arch interruption (usually in TA with TGV)." @default.