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)


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


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)

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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