2023 ICD-10-CM Diagnosis Code D68.09

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Other von Willebrand disease

    2023 - New Code Billable/Specific Code
  • D68.09 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • ICD-10-CM D68.09 is a new 2023 ICD-10-CM code that became effective on October 1, 2022.
  • This is the American ICD-10-CM version of D68.09 - other international versions of ICD-10 D68.09 may differ.
Applicable To
  • Platelet-type von Willebrand disease
  • Pseudo-von Willebrand disease
Code Also
Code Also Help
A code also note instructs that 2 codes may be required to fully describe a condition but the sequencing of the two codes is discretionary, depending on the severity of the conditions and the reason for the encounter.
  • , if applicable, qualitative platelet defects (
    ICD-10-CM Diagnosis Code D69.1

    Qualitative platelet defects

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    Applicable To
    • Bernard-Soulier [giant platelet] syndrome
    • Glanzmann's disease
    • Grey platelet syndrome
    • Thromboasthenia (hemorrhagic) (hereditary)
    • Thrombocytopathy
    Type 1 Excludes
    • hemolytic-uremic syndrome (D59.3-)
    Type 2 Excludes
    • von Willebrand disease (D68.0-)
    D69.1
    )
The following code(s) above D68.09 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 D68.09:
  • 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
ICD-10-CM D68.09 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 D68.09:
  • 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
      • platelet-type D68.09
      • pseudo D68.09
      • specified NEC D68.09

ICD-10-CM Codes Adjacent To D68.09
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
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

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