D68.020 Von Willebrand disease, type 2A

✓ Billable ICD-10-CM 2026
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The ICD-10-CM code for Von Willebrand disease, type 2A is D68.020 (FY2026). It is a billable, claim-ready diagnosis code.

Classification

Section
D65-D69: Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
Category D68
32 codes (25 billable)
FY2026 Status
Stable since FY2024

Also Known As

ICD-10-CM Alphabetic Index entries that lead to D68.020:

  • Defect, defective › qualitative, of von Willebrand factor › with › decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
  • Disease, diseased › von Willebrand (-Jürgens) (angiohemophilia) › type 2 › type 2A

Inclusion Terms

  • Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers

U.S. Hospital Utilization

  • An estimated 300 U.S. inpatient stays in 2023 included D68.020 among the documented diagnoses.

Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.

Official Coding Guidelines

Chapter 3 TOC entry

3. Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) ............................................................................................. 39

— ICD-10-CM Official Guidelines for Coding and Reporting, FY2026, Section I.C.3
Reserved for future guideline expansion

Reserved for future guideline expansion ...................................................................................... 39

— ICD-10-CM Official Guidelines for Coding and Reporting, FY2026, Section I.C.3.Reserved

Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026

References

Related Codes

Parent Code

D68 Other coagulation defects

Related Codes in D68

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 D68.021 Von Willebrand disease, type 2B D68.022 Von Willebrand disease, type 2M 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
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Reviewed by Prajwal Shrestha, CPC, CRC
Certified Professional Coder (CPC) and Certified Risk Adjustment Coder (CRC) · AAPC Member ID 01997614 · About · Editorial policy · Content last reviewed: 2025-10-01

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