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» D50-D89. Diseases of the blood & immune mechanism
» D65-D69. Coagulation defects, purpura and other haemorrhagic conditions
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D69. Purpura and other haemorrhagic conditions


Excludes: benign hypergammaglobulinaemic purpura ( D89.0 ) cryoglobulinaemic purpura ( D89.1 ) essential (haemorrhagic) thrombocythaemia ( D47.3 ) purpura fulminans ( D65 ) thrombotic thrombocytopenic purpura ( M31.1 ) D69.0 Allergic purpura Purpura: · anaphylactoid · Henoch(-Schönlein) · nonthrombocytopenic: · haemorrhagic · idiopathic · vascular Vasculitis, allergic D69.1 Qualitative platelet defects Bernard-Soulier [giant platelet] syndrome Glanzmann's disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy Excludes: von Willebrand's disease ( D68.0 ) D69.2 Other nonthrombocytopenic purpura Purpura: · NOS · senile · simplex D69.3 Idiopathic thrombocytopenic purpura Evans' syndrome D69.4 Other primary thrombocytopenia Excludes: thrombocytopenia with absent radius ( Q87.2 ) transient neonatal thrombocytopenia ( P61.0 ) Wiskott-Aldrich syndrome ( D82.0 ) D69.5 Secondary thrombocytopenia Use additional external cause code (Chapter XX), if desired, to identify cause. D69.6 Thrombocytopenia, unspecified D69.8 Other specified haemorrhagic conditions Capillary fragility (hereditary) Vascular pseudohaemophilia D69.9 Haemorrhagic condition, unspecified

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