ICD-10-CM Diagnosis Code (2025)
Official Description for D68.02
Von Willebrand disease, type 2
Coding Notes & Guidelines for D68.02
Qualitative defects of von Willebrand factor
Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
- Qualitative defects of von Willebrand factor with high-molecular-weight von Willebrand factor loss
- Qualitative defects of von Willebrand factor with hyper-adhesive forms
- Qualitative defects of von Willebrand factor with increased affinity for platelet glycoprotein lb
Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers
- Qualitative defects of von Willebrand factor with defective von Willebrand factor to factor VIII binding
- Qualitative defects of von Willebrand factor with markedly decreased affinity for factor VIII
Qualitative defect in von Willebrand factor function, with no further subtyping
Parent Code (Less Specific):
About ICD-10-CM Code D68.02 (Von Willebrand disease)
ICD-10-CM code D68.02 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM D68.02 became effective on October 1, 2024.
This page provides detailed information about D68.02 - Von Willebrand disease, type 2. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Von Willebrand disease related to type 2.