Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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(D65–D69) Coagulation defects, purpura and other haemorrhagic conditions[edit] |
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D65 |
Disseminated intravascular coagulation (defibrination syndrome) Afibrinogenaemia, acquired Consumption coagulopathy Diffuse or disseminated intravascular coagulation (DIC) Fibrinolytic haemorrhage, acquired Fibrinolytic purpura Purpura fulminans |
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D66 |
Hereditary factor VIII deficiency Haemophilia A |
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D67 |
Hereditary factor IX deficiency Christmas disease Haemophilia B |
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D68 |
Other coagulation defects |
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D68.0 |
Von Willebrand's disease |
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D68.1 |
Hereditary factor XI deficiency Haemophilia C |
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D68.2 |
Hereditary deficiency of other clotting factors |
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D68.3 |
Haemorrhagic disorder due to circulating anticoagulants |
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D68.4 |
Acquired coagulation factor deficiency Haemophilia A |
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D67 |
Hereditary factor IX deficiency Christmas disease Haemophilia B |
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D68 |
Other coagulation defects |
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D68.0 |
Von Willebrand's disease |
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D68.1 |
Hereditary factor XI deficiency Haemophilia C |
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D68.2 |
Hereditary deficiency of other clotting factors |
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D68.3 |
Haemorrhagic disorder due to circulating anticoagulants |
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D68.4 |
Acquired coagulation factor deficiency |
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D68.8 |
Other specified coagulation defects |
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D68.9 |
Coagulation defect, unspecified |
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D69 |
Purpura and other haemorrhagic conditions |
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D69.0 |
Allergic purpura anaphylactoid purpura Henoch-Schönlein purpura |
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D69.1 |
Qualitative platelet defects Bernard-Soulier syndrome (giant platelet) Glanzmann's disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy |
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D69.2 |
Other nonthrombocytopenic purpura |
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D69.3 |
Idiopathic thrombocytopenic purpura Evans' syndrome |
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D69.4 |
Other primary thrombocytopenia |
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D69.5 |
Secondary thrombocytopenia |
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D69.6 |
Thrombocytopenia, unspecified |
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D69.8 |
Other specified haemorrhagic conditions |
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D69.9 |
Haemorrhagic condition, unspecified |
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(D70–D77) Other diseases of blood and blood-forming organs |
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D70 |
Agranulocytosis Agranulocytic angina Infantile genetic agranulocytosis Kostmann's disease Neutropenia, NOS |
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D71 |
Functional disorders of polymorphonuclear neutrophils Cell membrane receptor complex (CR3) defect Chronic (childhood) granulomatous disease Congenital dysphagocytosis Progressive septic granulomatosis |
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D72 |
Other disorders of white blood cells |
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D72.0 |
Genetic anomalies of leukocytes Alder anomaly May-Hegglin anomaly Pelger-Huët anomaly |
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D72.1 |
Eosinophilia |
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D72.8 |
Other specified disorders of white blood cells Leukaemoid reaction: lymphocytic, monocytic, myelocytic Leukocytosis Lymphocytosis (symptomatic) Lymphopenia Monocytosis (symptomatic) Plasmacytosis |
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D72.9 |
Disorder of white blood cells, unspecified |
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D73 |
Diseases of spleen |
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D73.0 |
Hyposplenism |
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D73.1 |
Hypersplenism |
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D73.2 |
Chronic congestive splenomegaly |
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D73.3 |
Abscess of spleen |
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D73.4 |
Cyst of spleen |
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D73.5 |
Infarction of spleen |
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D73.8 |
Other diseases of spleen |
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D73.9 |
Disease of spleen, unspecified |
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D74 |
Methaemoglobinaemia |
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D74.0 |
Congenital methaemoglobinaemia Congenital NADH-methaemoglobin reductase deficiency Haemoglobin-M (Hb-M) disease Methaemoglobinaemia, hereditary |
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D74.8 |
Other methaemoglobinaemias Acquired methaemoglobinaemia (with sulfhaemoglobinaemia) Toxic methaemoglobinaemia |
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D74.9 |
Methaemoglobinaemia, unspecified |
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D75 |
Other diseases of blood and blood-forming organs |
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D75.0 |
Familial erythrocytosis |
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D75.1 |
Secondary polycythaemia |
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D75.2 |
Essential thrombocytosis |
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D75.8 |
Other specified diseases of blood and blood-forming organs Basophilia |
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D75.9 |
Disease of blood and blood-forming organs, unspecified |
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D76 |
Certain diseases involving lymphoreticular tissue and reticulohistiocytic system |
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D76.0 |
Langerhans' cell histiocytosis, not elsewhere classified Eosinophilic granuloma Hand-Schüller-Christian disease Histiocytosis X (chronic) |
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D76.1 |
Haemophagocytic lymphohistiocytosis Familial haemophagocytic reticulosis |
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D76.2 |
Haemophagocytic syndrome, infection-associated |
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D76.3 |
Other histiocytosis syndromes Reticulohistiocytoma (giant-cell) Sinus histiocytosis with massive lymphadenopathy Xanthogranuloma |
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D77 |
Other disorders of blood and blood-forming organs in diseases classified elsewhere |
