2023 ICD-10-CM Diagnosis Code D68.020

New Call-to-action

Von Willebrand disease, type 2A

    2023 - New Code Billable/Specific Code
  • D68.020 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • ICD-10-CM D68.020 is a new 2023 ICD-10-CM code that became effective on October 1, 2022.
  • This is the American ICD-10-CM version of D68.020 - other international versions of ICD-10 D68.020 may differ.
Applicable To
  • Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
The following code(s) above D68.020 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to D68.020:
  • D50-D89
    2023 ICD-10-CM Range D50-D89

    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

    Type 2 Excludes
    • autoimmune disease (systemic) NOS (M35.9)
    • certain conditions originating in the perinatal period (P00-P96)
    • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • endocrine, nutritional and metabolic diseases (E00-E88)
    • human immunodeficiency virus [HIV] disease (B20)
    • injury, poisoning and certain other consequences of external causes (S00-T88)
    • neoplasms (C00-D49)
    • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
  • D68
    ICD-10-CM Diagnosis Code D68

    Other coagulation defects

      2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • abnormal coagulation profile NOS (R79.1)
    Type 2 Excludes
    • coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
    • coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
    Other coagulation defects
  • D68.0
    ICD-10-CM Diagnosis Code D68.0

    Von Willebrand disease

      2016 2017 2018 2019 2020 2021 2022 2023 - Converted to Parent Code Non-Billable/Non-Specific Code
    Type 1 Excludes
    • capillary fragility (hereditary) (D69.8)
    • factor VIII deficiency NOS (D66)
    • factor VIII deficiency with functional defect (D66)
    Von Willebrand disease
  • D68.02
    ICD-10-CM Diagnosis Code D68.02

    Von Willebrand disease, type 2

      2023 - New Code Non-Billable/Non-Specific Code
    Applicable To
    • Qualitative defects of von Willebrand factor
    Von Willebrand disease, type 2
ICD-10-CM D68.020 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
  • 813 Coagulation disorders
Code History
  • 2023 (effective 10/1/2022): New code

Diagnosis Index entries containing back-references to D68.020:
  • Defect, defective Q89.9
    ICD-10-CM Diagnosis Code Q89.9

    Congenital malformation, unspecified

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital anomaly NOS
    • Congenital deformity NOS
  • Disease, diseased - see also Syndrome
    • von Willebrand (-Jürgens) (angiohemophilia) D68.00
      ICD-10-CM Diagnosis Code D68.00

      Von Willebrand disease, unspecified

        2023 - New Code Billable/Specific Code
      • type 2 D68.029
        ICD-10-CM Diagnosis Code D68.029

        Von Willebrand disease, type 2, unspecified

          2023 - New Code Billable/Specific Code
        Applicable To
        • Qualitative defect in von Willebrand factor function, with no further subtyping
        • type 2A D68.020

ICD-10-CM Codes Adjacent To D68.020
D64.89 Other specified anemias
D64.9 Anemia, unspecified
D65 Disseminated intravascular coagulation [defibrination syndrome]
D66 Hereditary factor VIII deficiency
D67 Hereditary factor IX deficiency
D68 Other coagulation defects
D68.0 Von Willebrand disease
D68.00 …… unspecified
D68.01 …… type 1
D68.02 Von Willebrand disease, type 2
D68.020 ……A
D68.021 ……B
D68.022 ……M
D68.023 ……N
D68.029 …… unspecified
D68.03 …… 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

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.