Tabular List. Categories and Subcategories of ICD-10
Tabular List. Categories and Subcategories of ICD-10 Tabular List. Categories and Subcategories of ICD-10
Tabular List. Categories and Subcategories of ICD-10 D58.8 Other specified hereditary haemolytic anaemias D58.9 Hereditary haemolytic anaemia, unspecified D59 Acquired haemolytic anaemia D59.0 Drug-induced autoimmune haemolytic anaemia D59.1 Other autoimmune haemolytic anaemias D59.2 Drug-induced nonautoimmune haemolytic anaemia D59.3 Haemolytic-uraemic syndrome D59.4 Other nonautoimmune haemolytic anaemias D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava- Micheli] D59.6 Haemoglobinuria due to haemolysis from other external causes D59.8 Other acquired haemolytic anaemias D59.9 Acquired haemolytic anaemia, unspecified D60 Acquired pure red cell aplasia [erythroblastopenia] D60.0 Chronic acquired pure red cell aplasia D60.1 Transient acquired pure red cell aplasia D60.8 Other acquired pure red cell aplasias D60.9 Acquired pure red cell aplasia, unspecified D61 Other aplastic anaemias D61.0 Constitutional aplastic anaemia D61.1 Drug-induced aplastic anaemia D61.2 Aplastic anaemia due to other external agents D61.3 Idiopathic aplastic anaemia D61.8 Other specified aplastic anaemias D61.9 Aplastic anaemia, unspecified D62 Acute posthaemorrhagic anaemia D63 Anaemia in chronic diseases classified elsewhere D63.0 Anaemia in neoplastic disease (C00-D48) D63.8 Anaemia in other chronic diseases classified elsewhere D64 Other anaemias D64.0 Hereditary sideroblastic anaemia D64.1 Secondary sideroblastic anaemia due to disease D64.2 Secondary sideroblastic anaemia due to drugs and toxins D64.3 Other sideroblastic anaemias D64.4 Congenital dyserythropoietic anaemia D64.8 Other specified anaemias D64.9 Anaemia, unspecified D65 Disseminated intravascular coagulation [defibrination syndrome] D66 Hereditary factor VIII deficiency D67 Hereditary factor IX deficiency D68 Other coagulation defects D68.0 Von Willebrand's disease D68.1 Hereditary factor XI deficiency D68.2 Hereditary deficiency of other clotting factors D68.3 Haemorrhagic disorder due to circulating anticoagulants D68.4 Acquired coagulation factor deficiency D68.8 Other specified coagulation defects D68.9 Coagulation defect, unspecified D69 Purpura and other haemorrhagic conditions D69.0 Allergic purpura D69.1 Qualitative platelet defects D69.2 Other nonthrombocytopenic purpura D69.3 Idiopathic thrombocytopenic purpura D69.4 Other primary thrombocytopenia D69.5 Secondary thrombocytopenia D69.6 Thrombocytopenia, unspecified 34
Tabular List. Categories and Subcategories of ICD-10 D69.8 Other specified haemorrhagic conditions D69.9 Haemorrhagic condition, unspecified D70 Agranulocytosis D71 Functional disorders of polymorphonuclear neutrophils D72 Other disorders of white blood cells D72.0 Genetic anomalies of leukocytes D72.1 Eosinophilia D72.8 Other specified disorders of white blood cells D72.9 Disorder of white blood cells, unspecified D73 Diseases of spleen D73.0 Hyposplenism D73.1 Hypersplenism D73.2 Chronic congestive splenomegaly D73.3 Abscess of spleen D73.4 Cyst of spleen D73.5 Infarction of spleen D73.8 Other diseases of spleen D73.9 Disease of spleen, unspecified D74 Methaemoglobinaemia D74.0 Congenital methaemoglobinaemia D74.8 Other methaemoglobinaemias D74.9 Methaemoglobinaemia, unspecified D75 Other diseases of blood and blood-forming organs D75.0 Familial erythrocytosis D75.1 Secondary polycythaemia D75.2 Essential thrombocytosis D75.8 Other specified diseases of blood and blood-forming organs D75.9 Disease of blood and blood-forming organs, unspecified D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system D76.0 Langerhans' cell histiocytosis, not elsewhere classified D76.1 Haemophagocytic lymphohistiocytosis D76.2 Haemophagocytic syndrome, infection-associated D76.3 Other histiocytosis syndromes D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere D80 Immunodeficiency with predominantly antibody defects D80.0 Hereditary hypogammaglobulinaemia D80.1 Nonfamilial hypogammaglobulinaemia D80.2 Selective deficiency of immunoglobulin A [IgA] D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses D80.4 Selective deficiency of immunoglobulin M [IgM] D80.5 Immunodeficiency with increased immunoglobulin M [IgM] D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia D80.7 Transient hypogammaglobulinaemia of infancy D80.8 Other immunodeficiencies with predominantly antibody defects D80.9 Immunodeficiency with predominantly antibody defects, unspecified D81 Combined immunodeficiencies D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis D81.1 Severe combined immunodeficiency [SCID] with low T- and B- cell numbers D81.2 Severe combined immunodeficiency [SCID] with low or normal B- cell numbers D81.3 Adenosine deaminase [ADA] deficiency D81.4 Nezelof's syndrome D81.5 Purine nucleoside phosphorylase [PNP] deficiency D81.6 Major histocompatibility complex class I deficiency D81.7 Major histocompatibility complex class II deficiency D81.8 Other combined immunodeficiencies 35
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<strong>Tabular</strong> <strong>List</strong>. <strong>Categories</strong> <strong>and</strong> <strong>Subcategories</strong> <strong>of</strong> <strong>ICD</strong>-<strong>10</strong><br />
D69.8 Other specified haemorrhagic conditions<br />
D69.9 Haemorrhagic condition, unspecified<br />
D70 Agranulocytosis<br />
D71 Functional disorders <strong>of</strong> polymorphonuclear neutrophils<br />
D72 Other disorders <strong>of</strong> white blood cells<br />
D72.0 Genetic anomalies <strong>of</strong> leukocytes<br />
D72.1 Eosinophilia<br />
D72.8 Other specified disorders <strong>of</strong> white blood cells<br />
D72.9 Disorder <strong>of</strong> white blood cells, unspecified<br />
D73 Diseases <strong>of</strong> spleen<br />
D73.0 Hyposplenism<br />
D73.1 Hypersplenism<br />
D73.2 Chronic congestive splenomegaly<br />
D73.3 Abscess <strong>of</strong> spleen<br />
D73.4 Cyst <strong>of</strong> spleen<br />
D73.5 Infarction <strong>of</strong> spleen<br />
D73.8 Other diseases <strong>of</strong> spleen<br />
D73.9 Disease <strong>of</strong> spleen, unspecified<br />
D74 Methaemoglobinaemia<br />
D74.0 Congenital methaemoglobinaemia<br />
D74.8 Other methaemoglobinaemias<br />
D74.9 Methaemoglobinaemia, unspecified<br />
D75 Other diseases <strong>of</strong> blood <strong>and</strong> blood-forming organs<br />
D75.0 Familial erythrocytosis<br />
D75.1 Secondary polycythaemia<br />
D75.2 Essential thrombocytosis<br />
D75.8 Other specified diseases <strong>of</strong> blood <strong>and</strong> blood-forming organs<br />
D75.9 Disease <strong>of</strong> blood <strong>and</strong> blood-forming organs, unspecified<br />
D76 Certain diseases involving lymphoreticular tissue <strong>and</strong> reticulohistiocytic system<br />
D76.0 Langerhans' cell histiocytosis, not elsewhere classified<br />
D76.1 Haemophagocytic lymphohistiocytosis<br />
D76.2 Haemophagocytic syndrome, infection-associated<br />
D76.3 Other histiocytosis syndromes<br />
D77 Other disorders <strong>of</strong> blood <strong>and</strong> blood-forming organs in diseases classified elsewhere<br />
D80 Immunodeficiency with predominantly antibody defects<br />
D80.0 Hereditary hypogammaglobulinaemia<br />
D80.1 Nonfamilial hypogammaglobulinaemia<br />
D80.2 Selective deficiency <strong>of</strong> immunoglobulin A [IgA]<br />
D80.3 Selective deficiency <strong>of</strong> immunoglobulin G [IgG] subclasses<br />
D80.4 Selective deficiency <strong>of</strong> immunoglobulin M [IgM]<br />
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]<br />
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia<br />
D80.7 Transient hypogammaglobulinaemia <strong>of</strong> infancy<br />
D80.8 Other immunodeficiencies with predominantly antibody defects<br />
D80.9 Immunodeficiency with predominantly antibody defects, unspecified<br />
D81 Combined immunodeficiencies<br />
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis<br />
D81.1 Severe combined immunodeficiency [SCID] with low T- <strong>and</strong> B- cell numbers<br />
D81.2 Severe combined immunodeficiency [SCID] with low or normal B- cell numbers<br />
D81.3 Adenosine deaminase [ADA] deficiency<br />
D81.4 Nezel<strong>of</strong>'s syndrome<br />
D81.5 Purine nucleoside phosphorylase [PNP] deficiency<br />
D81.6 Major histocompatibility complex class I deficiency<br />
D81.7 Major histocompatibility complex class II deficiency<br />
D81.8 Other combined immunodeficiencies<br />
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