{"orpha":248358,"name":"Rare thrombotic disorder due to a 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-248358/","orphanet_url":"https://www.orpha.net/en/disease/detail/248358","names":{"fr":{"name":"Maladie thrombotique rare par déficit en facteurs de coagulation"},"de":{"name":"Seltene thrombotische Störung durch Gerinnungsfaktoren-Defekt"},"es":{"name":"Enfermedad trombótica rara por un defecto de factores de coagulación"},"it":{"name":"Disturbo trombotico raro da difetto dei fattori di coagulazione"},"nl":{"name":"Zeldzame trombotische stoornis als gevolg van een coagulatiefactordefect"},"pt":{"name":"Doença trombótica rara por defeito nos fatores de coagulação"},"pl":{"name":"Rzadkie zaburzenie krzepnięcia z powodu defektu czynników krzepnięcia"},"cs":{"name":"Vzácné trombotické poruchy způsobené defektem koagulačních faktorů"},"uk":{"name":"Рідкісний тромботичний розлад, зумовлений дефектом факторів згортання крові"},"zh":{"name":"凝血因子缺陷所致罕见性血栓性疾病"},"tr":{"name":"Pıhtılaşma faktörleri defektine bağlı nadir trombotik bozukluk"}},"xrefs":[{"source":"MONDO","code":"16632","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680692","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":182054,"name":"Rare thrombotic disease of hematologic origin","classifications":[194]}],"children":[{"orpha":248361,"name":"Rare thrombotic disorder due to a constitutional coagulation factors defect","type":"Category"},{"orpha":248365,"name":"Rare thrombotic disorder due to an acquired coagulation factors defect","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}