D68.023
Von Willebrand disease, type 2N
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 defective von Willebrand factor to factor VIII binding Qualitative defects of von Willebrand factor with markedly decreased affinity for factor VIII
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 D68.023
FY 2026 ›Find D68.023 in the alphabetic index
3 index paths lead to this code