D69.59

Other secondary thrombocytopenia

Billable code

This code does not map to a risk-adjusting HCC in the loaded models.

Coding notes

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

Inherited from D69.5Secondary thrombocytopenia

Excludes 1

heparin induced thrombocytopenia (HIT) (D75.82-) transient thrombocytopenia of newborn (P61.0)

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 D69.59

FY 2026 ›

I.C.3Chapter-specific guidanceChapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)

Find D69.59 in the alphabetic index

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