{"orpha":98429,"name":"Rare coagulation disorder","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-98429/","orphanet_url":"https://www.orpha.net/en/disease/detail/98429","names":{"fr":{"name":"Coagulopathie rare"},"de":{"name":"Seltene Gerinnungsstörung"},"es":{"name":"Trastorno raro de la coagulación"},"it":{"name":"Difetto raro della coagulazione"},"nl":{"name":"Zeldzame coagulatiestoornis"},"pt":{"name":"Doença da coagulação, rara"},"pl":{"name":"Rzadkie zaburzenia koagulacji"},"cs":{"name":"Vzácné poruchy koagulace"},"uk":{"name":"Рідкісне порушення згортання крові"},"zh":{"name":"罕见凝血障碍"},"tr":{"name":"Nadir pıhtılaşma bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681721","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":97992,"name":"Rare hematologic disease","classifications":[194]}],"children":[{"orpha":717593,"name":"Disseminated intravascular coagulation associated with a vascular anomaly","type":"Particular clinical situation in a disease or syndrome"},{"orpha":717588,"name":"Localized intravascular coagulation","type":"Particular clinical situation in a disease or syndrome"},{"orpha":248308,"name":"Rare hemorrhagic disorder","type":"Category"},{"orpha":182054,"name":"Rare thrombotic disease of hematologic origin","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}