D69.9

Hemorrhagic condition, unspecified

Risk-adjusting (HCC)Billable code

HCC risk adjustment mapping

CMS-HCC ESRD V24

HCC48

Coagulation Defects and Other Specified Hematological Disorders

Coding notes

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

Inherited from D69Purpura and other hemorrhagic conditions
Excludes 1

benign hypergammaglobulinemic purpura (D89.0) cryoglobulinemic purpura (D89.1) essential (hemorrhagic) thrombocythemia (D47.3) hemorrhagic thrombocythemia (D47.3) purpura fulminans (D65) thrombotic thrombocytopenic purpura (M31.19) Waldenström hypergammaglobulinemic purpura (D89.0)

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 D69.9

FY 2026 ›