D68.021
Von Willebrand disease, type 2B
HCC risk adjustment mapping
CMS-HCC V28
Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions
CMS-HCC ESRD V24
Coagulation Defects and Other Specified Hematological Disorders
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
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
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)
Official Guidelines for D68.021
FY 2026 ›Find D68.021 in the alphabetic index
4 index paths lead to this code
- Defect, defective › qualitative, of von Willebrand factor › with › high-molecular-weight von Willebrand factor loss
- Defect, defective › qualitative, of von Willebrand factor › with › hyper-adhesive forms
- Defect, defective › qualitative, of von Willebrand factor › with › increased affinity for platelet glycoprotein lb
- Disease, diseased › von Willebrand › type 2 › type 2B