ICD-10 CM Code D69.42
D69.42
Congenital and hereditary thrombocytopenia purpura
Inclusion Term
- Congenital thrombocytopenia
- Hereditary thrombocytopenia
Excludes Type 1
- transient neonatal thrombocytopenia (P61.0)
- Wiskott-Aldrich syndrome (D82.0)
- benign hypergammaglobulinemic purpura (D89.0)
- cryoglobulinemic purpura (D89.1)
- essential (hemorrhagic) thrombocythemia (D47.3)
- hemorrhagic thrombocythemia (D47.3)
- purpura fulminans (D65)
- thrombotic thrombocytopenic purpura (M31.1)
- Waldenström hypergammaglobulinemic purpura (D89.0)
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