{"orpha":98718,"name":"Aortic malformation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-98718/","orphanet_url":"https://www.orpha.net/en/disease/detail/98718","names":{"fr":{"name":"Malformation aortique"},"de":{"name":"Aortenfehlbildung"},"es":{"name":"Malformación aórtica"},"it":{"name":"Malformazione aortica"},"nl":{"name":"Aortamalformatie"},"pt":{"name":"Malformação aórtica"},"pl":{"name":"Wada aorty"},"cs":{"name":"Aortální malformace"},"uk":{"name":"Мальформації аорти"},"zh":{"name":"主动脉畸形"},"tr":{"name":"Aort malformasyonu"}},"xrefs":[{"source":"UMLS","code":"C5681689","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":95449,"name":"OBSOLETE: Congenital aortic valve insufficiency","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98724,"name":"Congenital anomaly of the great arteries","classifications":[147,148,198]},{"orpha":98717,"name":"Transposition of the great arteries and conotruncal cardiac anomaly","classifications":[147,148]}],"children":[{"orpha":2299,"name":"Aortic arch interruption","type":"Morphological anomaly"},{"orpha":1457,"name":"Coarctation of aorta","type":"Morphological anomaly"},{"orpha":3093,"name":"Congenital aortic valve stenosis","type":"Morphological anomaly"},{"orpha":402075,"name":"Familial bicuspid aortic valve","type":"Morphological anomaly"},{"orpha":3092,"name":"Fixed subaortic stenosis","type":"Morphological anomaly"},{"orpha":1456,"name":"Middle aortic syndrome","type":"Morphological anomaly"},{"orpha":542568,"name":"Quadricuspid aortic valve","type":"Morphological anomaly"},{"orpha":3193,"name":"Supravalvular aortic stenosis","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}