D68.020ICD-10-CM 2027 · Billable
Von Willebrand disease, type 2A
Sibling codes
Inclusion terms
- Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
Inherited from D68.02: Von Willebrand disease, type 2
Inclusion terms
- Qualitative defects of von Willebrand factor
Inherited from D68.0: Von Willebrand disease
Excludes1
Inherited from D68: Other coagulation defects
Excludes1
- abnormal coagulation profile NOS (
R79.1)
Excludes2
Part of: D68.02: Von Willebrand disease, type 2 › D68.0: Von Willebrand disease › D68: Other coagulation defects