D68.023

Von Willebrand disease, type 2N

Risk-adjusting (HCC)Billable code

HCC risk adjustment mapping

CMS-HCC V28

HCC112

Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions

CMS-HCC ESRD V24

HCC48

Coagulation Defects and Other Specified Hematological Disorders

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

This code · D68.023
Synonyms

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

Inherited from D68.02Von Willebrand disease, type 2
Synonyms

Qualitative defects of von Willebrand factor

Inherited from D68.0Von Willebrand disease
Excludes 1

capillary fragility (hereditary) (D69.8) factor VIII deficiency NOS (D66) factor VIII deficiency with functional defect (D66)

Inherited from D68Other coagulation defects
Excludes 1

abnormal coagulation profile NOS (R79.1)

Excludes 2

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)

Inherited from chapter 3Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Excludes 2

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 ›