Medical Tests (32)

ICD10
D66Hereditary factor VIII deficiency
D67Hereditary factor IX deficiency
D68Other coagulation defects
D68.311Acquired hemophilia
Z13.7Encounter for screening for genetic and chromosomal anomalies
Z14.0Hemophilia A carrier
Z14.01Asymptomatic hemophilia A carrier
Z14.02Symptomatic hemophilia A carrier
Z83.2Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Additional ICD10
D68.0Von Willebrand's disease
D68.1Hereditary factor XI deficiency
D68.2Hereditary deficiency of other clotting factors
D68.3Hemorrhagic disorder due to circulating anticoagulants
D68.31Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.311Acquired hemophilia
D68.312Antiphospholipid antibody with hemorrhagic disorder
D68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4Acquired coagulation factor deficiency
D68.5Primary thrombophilia
D68.51Activated protein C resistance
D68.52Prothrombin gene mutation
D68.59Other primary thrombophilia
D68.6Other thrombophilia
D68.61Antiphospholipid syndrome
D68.62Lupus anticoagulant syndrome
D68.69Other thrombophilia
D68.8Other specified coagulation defects
D68.9Coagulation defect, unspecified

SNOMED
90935002Haemophilia