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Hereditary thrombophilia 439698008 SNOMED CT code SNOMED code 439698008 name Hereditary thrombophilia status active date introduced 2009-01-31 fully specified name(s) Hereditary thrombophilia (disorder) synonyms Hereditary thrombophilia Hereditary hypercoagulable disorder Primary thrombophilia attributes - group1 Interprets Hemostatic function 74848003 Has interpretation Abnormal 263654008 parents children Factor V Leiden mutation 307091009 Hereditary antithrombin III deficiency 439699000 Hereditary elevated factor VIII 441042008 Hereditary elevated factor XI 441001005 Hereditary heparin cofactor II deficiency 439701000 Hereditary hyperfibrinogenemia 440924009 Hereditary hyperhomocysteinemia 439006004 Hereditary protein C deficiency 439274008 Hereditary protein S deficiency 439702007 Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 783250007 Hereditary thrombophilic dysfibrinogenemia 438827002 Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 724344004 Prothrombin G20210A mutation 440989002 Resistance to activated protein C due to factor V Leiden mutation 421527008 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 118228005 362970003 234467004 439698008 138875005 404684003 64572001 782964007 32895009 439698008 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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