{"orpha":217454,"name":"Rare hereditary thrombophilia","type":"Clinical group","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-217454/","orphanet_url":"https://www.orpha.net/en/disease/detail/217454","names":{"fr":{"name":"Thrombophilie héréditaire rare"},"de":{"name":"Thrombophilie, hereditäre, seltene"},"es":{"name":"Trombofilia hereditaria rara"},"it":{"name":"Trombofilia ereditaria rara"},"nl":{"name":"Zeldzame erfelijke trombofilie"},"pt":{"name":"Trombofilia hereditária rara"},"pl":{"name":"Rzadka dziedziczna trombofilia"},"cs":{"name":"Vzácná hereditární trombofilie"},"uk":{"name":"Рідкісна спадкова тромбофілія"},"zh":{"name":"罕见遗传性血栓形成"},"tr":{"name":"Nadir kalıtsal trombofili"}},"xrefs":[{"source":"MONDO","code":"16320","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680871","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":399185,"name":"Rare hereditary disease with avascular necrosis","classifications":[156,196,199]},{"orpha":248361,"name":"Rare thrombotic disorder due to a constitutional coagulation factors defect","classifications":[156,194]}],"children":[{"orpha":82,"name":"Hereditary thrombophilia due to congenital antithrombin deficiency","type":"Disease"},{"orpha":217467,"name":"Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency","type":"Disease"},{"orpha":745,"name":"Severe hereditary thrombophilia due to congenital protein C deficiency","type":"Disease"},{"orpha":743,"name":"Severe hereditary thrombophilia due to congenital protein S deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}