Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
D75 Other diseases of blood and blood-forming organs Excludes: enlarged lymph nodes ( R59.- ) hypergammaglobulinaemia NOS ( D89.2 ) lymphadenitis: · NOS ( I88.9 ) · acute ( L04.- ) · chronic ( I88.1 ) · mesenteric (acute)(chronic) ( I88.0 ) D75.0 Familial erythrocytosis Polycythaemia: · benign · familial Excludes: hereditary ovalocytosis ( D58.1 ) D75.1 Secondary polycythaemia Erythrocytosis NOS Polycythaemia: · acquired · due to: · erythropoietin · fall in plasma volume · high altitude · stress · emotional · hypoxaemic · nephrogenous · relative Excludes: polycythaemia: · neonatorum ( P61.1 ) · vera ( D45 ) D75.2 Essential thrombocytosis Excludes: essential (haemorrhagic) thrombocythaemia ( D47.3 ) D75.8 Other specified diseases of blood and blood-forming organs Basophilia D75.9 Disease of blood and blood-forming organs, unspecified D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system Excludes: Letterer-Siwe disease ( C96.0 ) malignant histiocytosis ( C96.1 ) reticuloendotheliosis or reticulosis: · histiocytic medullary (C96.1 ) · leukaemic ( C91.4 ) · lipomelanotic ( I89.8 ) · malignant ( C85.7 ) · nonlipid ( C96.0 ) 136 WHO’s ICD-10
D76.0 Langerhans' cell histiocytosis, not elsewhere classified Eosinophilic granuloma Hand-Schüller-Christian disease Histiocytosis X (chronic) D76.1 Haemophagocytic lymphohistiocytosis Familial haemophagocytic reticulosis Histiocytoses of mononuclear phagocytes other than Langerhans' cells NOS D76.2 Haemophagocytic syndrome, infection-associated Use additional code, if desired, to identify infectious agent or disease D76.3 Other histiocytosis syndromes Reticulohistiocytoma (giant-cell) Sinus histiocytosis with massive lymphadenopathy Xanthogranuloma D77* Other disorders of blood and blood-forming organs in diseases classified elsewhere Fibrosis of spleen in schistosomiasis [bilharziasis] ( B65.-† ) Certain disorders involving the immune mechanism (D80-D89) Includes: defects in the complement system immunodeficiency disorders, except human immunodeficiency virus [HIV] disease sarcoidosis Excludes: autoimmune disease (systemic) NOS ( M35.9 ) functional disorders of polymorphonuclear neutrophils ( D71 ) human immunodeficiency virus [HIV] disease ( B20-B24 ) D80 Immunodeficiency with predominantly antibody defects D80.0 Hereditary hypogammaglobulinaemia Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency) D80.1 Nonfamilial hypogammaglobulinaemia Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS 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 Kappa light chain deficiency D80.9 Immunodeficiency with predominantly antibody defects, unspecified Version for 2007 137
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- Page 91 and 92: C49 Malignant neoplasm of other con
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D75<br />
Other <strong>diseases</strong> of blood <strong>and</strong> blood-forming organs<br />
Excludes: enlarged lymph nodes ( R59.- )<br />
hypergammaglobulinaemia NOS ( D89.2 )<br />
lymphadenitis:<br />
· NOS ( I88.9 )<br />
· acute ( L04.- )<br />
· chronic ( I88.1 )<br />
· mesenteric (acute)(chronic) ( I88.0 )<br />
D75.0 Familial erythrocytosis<br />
Polycythaemia:<br />
· benign<br />
· familial<br />
Excludes: hereditary ovalocytosis ( D58.1 )<br />
D75.1 Secondary polycythaemia<br />
Erythrocytosis NOS<br />
Polycythaemia:<br />
· acquired<br />
· due to:<br />
· erythropoietin<br />
· fall in plasma volume<br />
· high altitude<br />
· stress<br />
· emotional<br />
· hypoxaemic<br />
· nephrogenous<br />
· relative<br />
Excludes:<br />
polycythaemia:<br />
· neonatorum ( P61.1 )<br />
· vera ( D45 )<br />
D75.2 Essential thrombocytosis<br />
Excludes: essential (haemorrhagic) thrombocythaemia ( D47.3 )<br />
D75.8 Other specified <strong>diseases</strong> of blood <strong>and</strong> blood-forming organs<br />
Basophilia<br />
D75.9 Disease of blood <strong>and</strong> blood-forming organs, unspecified<br />
D76<br />
<strong>Certain</strong> <strong>diseases</strong> involving lymphoreticular tissue <strong>and</strong><br />
reticulohistiocytic system<br />
Excludes: Letterer-Siwe disease ( C96.0 )<br />
malignant histiocytosis ( C96.1 )<br />
reticuloendotheliosis or reticulosis:<br />
· histiocytic medullary (C96.1 )<br />
· leukaemic ( C91.4 )<br />
· lipomelanotic ( I89.8 )<br />
· malignant ( C85.7 )<br />
· nonlipid ( C96.0 )<br />
136 WHO’s ICD-10