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D68.09 Other von Willebrand disease

BackD68Other coagulation defects9 →D68.0Von Willebrand disease6 →D68.00Von Willebrand disease, unspecifiedD68.01Von Willebrand disease, type 1D68.02Von Willebrand disease, type 25 →D68.020Von Willebrand disease, type 2AD68.021Von Willebrand disease, type 2BD68.022Von Willebrand disease, type 2MD68.023Von Willebrand disease, type 2ND68.029Von Willebrand disease, type 2, unspecifiedD68.03Von Willebrand disease, type 3D68.04Acquired von Willebrand diseaseD68.09Other von Willebrand diseaseD68.1Hereditary factor XI deficiencyD68.2Hereditary deficiency of other clotting factorsD68.3Hemorrhagic disorder due to circulating anticoagulants2 →D68.31Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors3 →D68.311Acquired hemophiliaD68.312Antiphospholipid antibody with hemorrhagic disorderD68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitorsD68.32Hemorrhagic disorder due to extrinsic circulating anticoagulantsD68.4Acquired coagulation factor deficiencyD68.5Primary thrombophilia3 →D68.51Activated protein C resistanceD68.52Prothrombin gene mutationD68.59Other primary thrombophiliaD68.6Other thrombophilia3 →D68.61Antiphospholipid syndromeD68.62Lupus anticoagulant syndromeD68.69Other thrombophiliaD68.8Other specified coagulation defectsD68.9Coagulation defect, unspecified
CategoryCODABLE
D68.09
Other von Willebrand disease
EXAMPLES
Platelet-type von Willebrand disease
Pseudo-von Willebrand disease
CODING RULE
Code also: , if applicable, qualitative platelet defects (D69.1)
Chapter
III · Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Section
D65-D69
Valid from
Source

CMS ICD-10-CM Tabular List, edition FY2026.

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