{"orpha":3160,"name":"OBSOLETE: Vascular disruption sequence","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare developmental defect during embryogenesis","url":"https://raremap.alftech.space/d/ORPHA-3160/","orphanet_url":"https://www.orpha.net/en/disease/detail/3160","names":{"fr":{"name":"OBSOLETE : Séquence de disruption vasculaire"},"de":{"name":"OBSOLET: Vaskuläre Gefäßunterbrechung"},"es":{"name":"OBSOLETO: Secuencia de disrupción vascular"},"it":{"name":"OBSOLETO: Sequenza da amputazione vascolare"},"nl":{"name":"OBSOLEET: Vasculaire disruptiesequentie"},"pt":{"name":"OBSOLETO: Sequência de disrupção vascular"},"pl":{"name":"NIEAKTUALNE: Sekwencja dysrupcji naczyniowej"},"cs":{"name":"NEAKTUÁLNÍ: Sekvence přerušení cév"},"uk":{"name":"ЗАСТАРІЛО: Послідовність судинних порушень"},"zh":{"name":"弃用：血管破坏序列征"},"tr":{"name":"Eski adı: Vasküler bozulma dizisi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93890,"name":"Rare developmental defect during embryogenesis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}