{"orpha":458844,"name":"Rare vascular malformation of major vessels","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-458844/","orphanet_url":"https://www.orpha.net/en/disease/detail/458844","names":{"fr":{"name":"Malformation vasculaire rare des gros vaisseaux"},"de":{"name":"Seltene vaskuläre Fehlbildung der grossen Gefässe","synonyms":["Seltene vaskuläre Malformation der grossen Gefässe"]},"es":{"name":"Malformación vascular rara de los grandes vasos"},"it":{"name":"Malformazione vascolare dei grossi vasi"},"nl":{"name":"Zeldzame vasculaire malformatie van grote bloedvaten"},"pt":{"name":"Malformação vascular de grandes vasos"},"pl":{"name":"Rzadka malformacja dużych naczyń"},"cs":{"name":"Vzácné vaskulární malformace postihující velké cévy"},"uk":{"name":"Рідкісна судинна вада розвитку магістральних судин"},"zh":{"name":"罕见大血管畸形"},"tr":{"name":"Ana damarların nadir vasküler malformasyonu"}},"xrefs":[{"source":"MONDO","code":"18723","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681117","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":68419,"name":"Rare vascular anomaly","classifications":[147,198]}],"children":[{"orpha":698260,"name":"Carotid web","type":"Disease"},{"orpha":98724,"name":"Congenital anomaly of the great arteries","type":"Category"},{"orpha":363189,"name":"Congenital anomaly of the great veins","type":"Category"},{"orpha":97598,"name":"Congenital renal artery stenosis","type":"Disease"},{"orpha":494424,"name":"Extracranial carotid artery aneurysm","type":"Morphological anomaly"},{"orpha":981,"name":"Internal carotid absence","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}