{"orpha":248365,"name":"Rare thrombotic disorder due to an acquired coagulation factors defect","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-248365/","orphanet_url":"https://www.orpha.net/en/disease/detail/248365","names":{"fr":{"name":"Maladie thrombotique rare par déficit acquis en facteurs de coagulation"},"de":{"name":"Seltene thrombotische Störung durch erworbenen Gerinnungsfaktoren-Defekt"},"es":{"name":"Enfermedad trombótica rara por un defecto adquirido de los factores de coagulación"},"it":{"name":"Disturbo trombotico raro da difetto acquisito dei fattori di coagulazione"},"nl":{"name":"Zeldzame trombotische stoornis als gevolg van een verworven coagulatiefactordefect"},"pt":{"name":"Doença trombótica rara por defeito adquirido nos fatores de coagulação"},"pl":{"name":"Rzadkie zaburzenie krzepnięcia z powodu nabytego defektu czynników krzepnięcia"},"cs":{"name":"Vzácné poruchy srážlivosti způsobené získanou poruchou koagulačních faktorů"},"uk":{"name":"Рідкісний тромботичний розлад, зумовлений набутим дефектом факторів згортання крові"},"zh":{"name":"获得性凝血因子缺陷所致罕见性血栓性疾病"},"tr":{"name":"Edinsel pıhtılaşma faktörleri defektine bağlı nadir trombotik bozukluk"}},"xrefs":[{"source":"MONDO","code":"16634","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680688","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":248358,"name":"Rare thrombotic disorder due to a coagulation factors defect","classifications":[194]}],"children":[{"orpha":49566,"name":"Acquired purpura fulminans","type":"Disease"},{"orpha":80,"name":"Antiphospholipid syndrome","type":"Disease"},{"orpha":464343,"name":"Catastrophic antiphospholipid syndrome","type":"Disease"},{"orpha":26349,"name":"Protein S acquired deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}