Child codes (5)
More specific codes that fall directly under D68.02.
Code family — category D68
Every other code sharing category D68, for context when choosing between close variants.
Other coagulation defects
Von Willebrand disease
Von Willebrand disease, unspecified
Von Willebrand disease, type 1
Von Willebrand disease, type 2A
Von Willebrand disease, type 2B
Von Willebrand disease, type 2M
Von Willebrand disease, type 2N
Von Willebrand disease, type 2, unspecified
Von Willebrand disease, type 3
Acquired von Willebrand disease
Other von Willebrand disease
Hereditary factor XI deficiency
Hereditary deficiency of other clotting factors
Hemorrhagic disorder due to circulating anticoagulants
Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
Acquired hemophilia
Antiphospholipid antibody with hemorrhagic disorder
Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
Hemorrhagic disorder due to extrinsic circulating anticoagulants
Acquired coagulation factor deficiency
Primary thrombophilia
Activated protein C resistance
Prothrombin gene mutation
Other primary thrombophilia
Other thrombophilia
Antiphospholipid syndrome
Lupus anticoagulant syndrome
Other thrombophilia
Other specified coagulation defects
Coagulation defect, unspecified
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Patientary is an informational reference tool built on public data (CMS NPPES and the official ICD-10-CM release). It is not medical, coding, legal or billing advice, and code assignment is the responsibility of a qualified professional. Always verify against the primary source before you bill or file.