Diagnosis Code

D68.022 VON WILLEBRAND DISEASE, TYPE 2M


Code Information

Diagnosis Code: D68.022

Short Description: Von Willebrand disease, type 2M

Long Description: Von Willebrand disease, type 2M

The code D68.022 is VALID for claim submission

Code Classification:

  • Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
    • Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
      • Other coagulation defects (D68)
        • D68.022 Von Willebrand disease, type 2M

Code Version: 2022 ICD-10-CM


Synonyms

  • Hereditary von Willebrand disease
  • Hereditary von Willebrand disease type 2
  • Hereditary von Willebrand disease type 2M

References to Index of Diseases and Injuries

The code D68.022 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers

Similar Codes

ICD-10 Code ICD-10 Description
D68 Other coagulation defects
D68.0 Von Willebrand disease
D68.00 Von Willebrand disease, unspecified
D68.01 Von Willebrand disease, type 1
D68.02 Von Willebrand disease, type 2
D68.020 Von Willebrand disease, type 2A
D68.021 Von Willebrand disease, type 2B
D68.023 Von Willebrand disease, type 2N
D68.029 Von Willebrand disease, type 2, unspecified
D68.03 Von Willebrand disease, type 3
D68.04 Acquired von Willebrand disease
D68.09 Other von Willebrand disease
D68.1 Hereditary factor XI deficiency
D68.2 Hereditary deficiency of other clotting factors
D68.3 Hemorrhagic disorder due to circulating anticoagulants
D68.31 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.311 Acquired hemophilia
D68.312 Antiphospholipid antibody with hemorrhagic disorder
D68.318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32 Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4 Acquired coagulation factor deficiency
D68.5 Primary thrombophilia
D68.51 Activated protein C resistance
D68.52 Prothrombin gene mutation
D68.59 Other primary thrombophilia
D68.6 Other thrombophilia
D68.61 Antiphospholipid syndrome
D68.62 Lupus anticoagulant syndrome
D68.69 Other thrombophilia
D68.8 Other specified coagulation defects
D68.9 Coagulation defect, unspecified


This page was last updated on: 10/1/2023