Chapter III
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
(D50-D89)
Other diseases of blood and blood-forming organs
(D70-D77)
| D70 | Agranulocytosis Latin: Agranulocytosis | |||||||
| Agranulocytic angina Infantile genetic agranulocytosis Kostmann's disease Neutropenia: · NOS · congenital · cyclic · drug-induced · periodic · splenic (primary) · toxic Neutropenic splenomegaly | ||||||||
| Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced. | ||||||||
| Excludes: | transient neonatal neutropenia (P61.5) | |||||||
| D71 | Functional disorders of polymorphonuclear neutrophils Latin: Dysfunctiones cellularum neutrophilorum polymorphonucleorum | |||||||
| Cell membrane receptor complex [CR3] defect Chronic (childhood) granulomatous disease Congenital dysphagocytosis Progressive septic granulomatosis | ||||||||
| D72 | Other disorders of white blood cells Latin: Morbi leucocytorum alii | |||||||
| Excludes: | basophilia (D75.8) immunity disorders (D80-D89) neutropenia (D70) preleukaemia (syndrome) (D46.9) | |||||||
| D72.0 | Genetic anomalies of leukocytes | |||||||
| Anomaly (granulation)(granulocyte) or syndrome: · Alder · May-Hegglin · Pelger-Huët Hereditary: · leukocytic: · hypersegmentation · hyposegmentation · leukomelanopathy | ||||||||
| Excludes: | Chediak(-Steinbrinck)-Higashi syndrome (E70.3) | |||||||
| D72.1 | Eosinophilia | |||||||
| Eosinophilia: · allergic · hereditary | ||||||||
| D72.8 | Other specified disorders of white blood cells | |||||||
| Leukaemoid reaction: · lymphocytic · monocytic · myelocytic Leukocytosis Lymphocytosis (symptomatic) Lymphopenia Monocytosis (symptomatic) Plasmacytosis | ||||||||
| D72.9 | Disorder of white blood cells, unspecified | |||||||
| D73 | Diseases of spleen Latin: Morbus splenis | |||||||
| D73.0 | Hyposplenism | |||||||
| Asplenia, postsurgical Atrophy of spleen | ||||||||
| Excludes: | asplenia (congenital) (Q89.0) | |||||||
| D73.1 | Hypersplenism | |||||||
| Excludes: | splenomegaly: · NOS (R16.1) · congenital (Q89.0) | |||||||
| D73.2 | Chronic congestive splenomegaly | |||||||
| D73.3 | Abscess of spleen | |||||||
| D73.4 | Cyst of spleen | |||||||
| D73.5 | Infarction of spleen | |||||||
| Splenic rupture, nontraumatic Torsion of spleen | ||||||||
| Excludes: | traumatic rupture of spleen (S36.0) | |||||||
| D73.8 | Other diseases of spleen | |||||||
| Fibrosis of spleen NOS Perisplenitis Splenitis NOS | ||||||||
| D73.9 | Disease of spleen, unspecified | |||||||
| D74 | Methaemoglobinaemia Latin: Methaemoglobinaemia | |||||||
| D74.0 | Congenital methaemoglobinaemia | |||||||
| Congenital NADH-methaemoglobin reductase deficiency Haemoglobin-M [Hb-M] disease Methaemoglobinaemia, hereditary | ||||||||
| D74.8 | Other methaemoglobinaemias | |||||||
| Acquired methaemoglobinaemia (with sulfhaemoglobinaemia) Toxic methaemoglobinaemia | ||||||||
| Use additional external cause code (Chapter XX), if desired, to identify cause. | ||||||||
| D74.9 | Methaemoglobinaemia, unspecified | |||||||
| D75 | Other diseases of blood and blood-forming organs Latin: Morbi sanguinis et morbi systematis haematopoietici alii | |||||||
| 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 Latin: Morbi telae lymphoreticularis et morbi systematis reticulohistiocytici | |||||||
| 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) | |||||||
| 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 Latin: Disordines sanguinis et disordines systematis haematipoietici alii in morbis aliis | |||||||
| Fibrosis of spleen in schistosomiasis [bilharziasis] (B65.-+) | ||||||||
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