D69 |
 |
Purpura and other hemorrhagic conditions  |
| |
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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D69.0 |
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Allergic purpura |
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Allergic vasculitis | Nonthrombocytopenic hemorrhagic purpura | Nonthrombocytopenic idiopathic purpura | Purpura anaphylactoid | Purpura Henoch(-Schönlein) | Purpura rheumatica | Vascular purpura |
Excludes1 |
thrombocytopenic hemorrhagic purpura (D69.3)
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D69.1 |
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Qualitative platelet defects |
| |
Bernard-Soulier [giant platelet] syndrome | Glanzmann's disease | Grey platelet syndrome | Thromboasthenia (hemorrhagic) (hereditary) | Thrombocytopathy |
Excludes1 |
hemolytic-uremic syndrome (D59.3-)
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Excludes2 |
von Willebrand disease (D68.0-)
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D69.2 |
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Other nonthrombocytopenic purpura |
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Purpura NOS | Purpura simplex | Senile purpura |
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D69.3 |
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Immune thrombocytopenic purpura |
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Hemorrhagic (thrombocytopenic) purpura | Idiopathic thrombocytopenic purpura | Tidal platelet dysgenesis |
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D69.4 |
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Other primary thrombocytopenia |
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Excludes1 |
transient neonatal thrombocytopenia (P61.0) Wiskott-Aldrich syndrome (D82.0)
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D69.41 |
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Evans syndrome |
| | |
D69.42 |
 |
Congenital and hereditary thrombocytopenia purpura |
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Congenital thrombocytopenia | Hereditary thrombocytopenia |
CodeFirst |
congential or hereditary disorder, such as: thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
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|
| | |
D69.49 |
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Other primary thrombocytopenia |
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Megakaryocytic hypoplasia | Primary thrombocytopenia NOS |
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D69.5 |
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Secondary thrombocytopenia |
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Excludes1 |
heparin induced thrombocytopenia (HIT) (D75.82-) transient thrombocytopenia of newborn (P61.0)
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|
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D69.51 |
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Posttransfusion purpura |
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Posttransfusion purpura from whole blood (fresh) or blood products | PTP |
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D69.59 |
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Other secondary thrombocytopenia |
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D69.6 |
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Thrombocytopenia, unspecified |
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D69.8 |
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Other specified hemorrhagic conditions |
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Capillary fragility (hereditary) | Vascular pseudohemophilia |
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D69.9 |
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Hemorrhagic condition, unspecified |
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