ICD-10-CM Code for Congenital and hereditary thrombocytopenia purpura D69.42

ICD-10 code D69.42 for Congenital and hereditary thrombocytopenia purpura is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

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Congenital and hereditary thrombocytopenia purpura
Congenital thrombocytopenia
Hereditary thrombocytopenia
Code first congential or hereditary disorder, such as:
thrombocytopenia with absent radius (TAR syndrome) (Q87.2)

D69.4

Excludes1: transient neonatal thrombocytopenia (P61.0)
Wiskott-Aldrich syndrome (D82.0)

D69

Excludes1: 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)

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Get crucial instructions for accurate ICD-10-CM D69.42 coding with all applicable Excludes 1 and Excludes 2 notes from the section level conveniently shown with each code.
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