{"orpha":1132,"name":"Aortic arch defects","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-1132/","orphanet_url":"https://www.orpha.net/en/disease/detail/1132","names":{"fr":{"name":"Arcs aortiques anormaux"},"de":{"name":"Aortenbogen-Defekte"},"es":{"name":"Arcos aórticos anómalos"},"it":{"name":"Anomalie dell'arco aortico"},"nl":{"name":"Aortaboogdefecten"},"pt":{"name":"Anomalia do arco aórtico"},"pl":{"name":"Wady łuku aorty"},"cs":{"name":"Defekt aortálního oblouku"},"uk":{"name":"Вади дуги аорти"},"zh":{"name":"主动脉弓中断"},"tr":{"name":"Aortik ark defekti"}},"xrefs":[{"source":"MONDO","code":"0015236","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15236","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680872","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"741","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98724,"name":"Congenital anomaly of the great arteries","classifications":[147,148,198]}],"children":[{"orpha":99079,"name":"Cervical aortic arch","type":"Morphological anomaly"},{"orpha":99082,"name":"Dysphagia lusoria","type":"Morphological anomaly"},{"orpha":99075,"name":"Encircling double aortic arch","type":"Morphological anomaly"},{"orpha":99077,"name":"Kommerell diverticulum","type":"Morphological anomaly"},{"orpha":99078,"name":"Neuhauser anomaly","type":"Morphological anomaly"},{"orpha":99076,"name":"Persistent fifth aortic arch","type":"Morphological anomaly"},{"orpha":99081,"name":"Right aortic arch","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Childhood"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}