ICD-10 Code D68.020 – Von Willebrand disease, type 2A (2026): Diagnosis, Symptoms & Billing Guide
2026 ICD-10-CM Diagnosis Code D68.020 – Von Willebrand disease, type 2A
What it is
D68.020 identifies type 2A von Willebrand disease, an inherited bleeding disorder caused by abnormal von Willebrand factor function. It reduces normal platelet adhesion and can lead to mucocutaneous bleeding.
Clinical signs
Clinical features vary; refer to documentation. Common findings include easy bruising, frequent nosebleeds, prolonged bleeding after minor injury, and heavy menstrual bleeding. Diagnosis is typically supported by laboratory and hematology evaluation.
When to use this code
Use this code when the provider documents von Willebrand disease, type 2A, or confirms this subtype in the assessment. It also fits follow-up visits for known disease when the subtype remains active and relevant to care.
If the record only says von Willebrand disease without a subtype, you should not assume type 2A. Check documentation for the exact variant before assigning this code.
Do not use for
Do not use D68.020 for other von Willebrand disease subtypes, acquired bleeding disorders, or nonspecific “bleeding tendency” notes. Check documentation if the subtype is unclear.
Coding tip
Always code the documented subtype exactly; if type 2A is not stated, query or use the unspecified von Willebrand disease code as supported.