D70 | 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
|
D72 | Other disorders of white blood cells | |||||||
Excludes: | basophilia
immunity disorders neutropenia preleukaemia (syndrome) |
|||||||
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
|
|||||||
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 | |||||||
D73.0 | Hyposplenism | |||||||
Asplenia, postsurgical
Atrophy of spleen |
||||||||
Excludes: | asplenia (congenital)
|
|||||||
D73.1 | Hypersplenism | |||||||
Excludes: | splenomegaly:
· NOS · congenital |
|||||||
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
|
|||||||
D73.8 | Other diseases of spleen | |||||||
Fibrosis of spleen NOS
Perisplenitis Splenitis NOS |
||||||||
D73.9 | Disease of spleen, unspecified |
D75 | Other diseases of blood and blood-forming organs | |||||||
Excludes: | enlarged lymph nodes
hypergammaglobulinaemia NOS lymphadenitis: · NOS · acute · chronic · mesenteric (acute)(chronic) |
|||||||
D75.0 | Familial erythrocytosis | |||||||
Polycythaemia:
· benign · familial |
||||||||
Excludes: | hereditary ovalocytosis
|
|||||||
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 · vera |
|||||||
D75.2 | Essential thrombocytosis | |||||||
Excludes: | essential (haemorrhagic) thrombocythaemia
|
|||||||
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
malignant histiocytosis reticuloendotheliosis or reticulosis: · histiocytic medullary · leukaemic · lipomelanotic · malignant · nonlipid |
|||||||
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]
|