{"orpha":1138,"name":"Abnormal origin of the pulmonary artery","type":"Clinical group","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-1138/","orphanet_url":"https://www.orpha.net/en/disease/detail/1138","names":{"fr":{"name":"Artère pulmonaire d'origine anormale"},"de":{"name":"Pulmonalarterie, abnormaler Ursprung"},"es":{"name":"Arteria pulmonar naciente de la aorta"},"it":{"name":"Arteria polmonare ad origine anomala"},"nl":{"name":"Abnormale oorsprong van arteria pulmonalis","synonyms":["Abnormale oorsprong van longslagader"]},"pt":{"name":"Artéria pulmonar com origem na aorta"},"pl":{"name":"Nieprawidłowe pochodzenie tętnicy płucnej"},"cs":{"name":"Abnormální počátek plicní arterie"},"uk":{"name":"Аномальне відходження легеневої артерії"},"zh":{"name":"肺动脉起源异常"},"tr":{"name":"Pulmoner arterin anormal kökeni"}},"xrefs":[{"source":"ICD-11","code":"LA8B.1","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"953235173"},{"source":"MONDO","code":"0015239","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15239","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0265912","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":2445,"name":"Conotruncal heart malformations","classifications":[147,148]}],"children":[{"orpha":99050,"name":"Abnormal origin of right or left pulmonary artery from the aorta","type":"Morphological anomaly"},{"orpha":658574,"name":"Isolated pulmonary artery sling","type":"Morphological anomaly"},{"orpha":99049,"name":"Pulmonary artery coming from patent ductus arteriosus","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}