ICD-10-CM › D68 › D68.0 › D68.02 D68.022 Von Willebrand disease, type 2MBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Applicable to Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers Applies from D68 Other coagulation defects Excludes1 (never code together) abnormal coagulation profile NOS (R79.1) Excludes2 (not included here) coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1) coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3) Applies from D68.0 Von Willebrand disease Excludes1 (never code together) capillary fragility (hereditary) (D69.8) factor VIII deficiency NOS (D66) factor VIII deficiency with functional defect (D66) Applies from D68.02 Von Willebrand disease, type 2 Applicable to Qualitative defects of von Willebrand factor Risk adjustment (HCC) CMS-HCC V28: HCC 112 — Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions CMS-HCC V22: HCC 48 — Coagulation Defects and Other Specified Hematological Disorders ESRD V24: HCC 48 MS-DRG index Defines the logic of DRG(s) 813 in MDC 16.
Code annotations containing back-references to D68.022 Back-references to D68.0 Type 1 Excludes: D66 Type 2 Excludes: D69.1 Code First: M36.2 Type 1 Excludes: R04.81 Back-references to D68 Type 1 Excludes: R79.1 Diagnosis Index entries for D68.022 Defect, defective › qualitative, of von Willebrand factor › with › defective platelet adhesion with a normal size distribution of von Willebrand factor multimers Disease, diseased › von Willebrand (-Jürgens) (angiohemophilia) › type 2 › type 2M Nearby codes D68.00D68.01D68.02D68.020D68.021D68.022 Von Willebrand disease, type 2M (this code)D68.023D68.029D68.03D68.04D68.09