D68.5
Primary thrombophilia
Coding guidance (WHO 2019)
Activated protein C resistance [factor V Leiden mutation] Deficiency: antithrombin protein C protein S Prothrombin gene mutation
Sibling codes
D68Other coagulation defectsD68.0Von Willebrand diseaseD68.1Hereditary factor XI deficiencyD68.2Hereditary deficiency of other clotting factorsD68.3Haemorrhagic disorder due to circulating anticoagulantsD68.4Acquired coagulation factor deficiencyD68.6Other thrombophiliaD68.8Other specified coagulation defectsD68.9Coagulation defect, unspecified