A00-B99 C00-D48D50-D89 E00-E90 F00-F99 G00-G99 H00-H59 H60-H95 I00-I99 J00-J99 K00-K93
L00-L99 M00-M99 N00-N99 O00-O99 P00-P96 Q00-Q99 R00-R99 S00-T98 V01-Y98 Z00-Z99 U00-U99

D70-D77 Other diseases of blood and blood-forming organs




 
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)

D70Agranulocytosis
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)

D71Functional disorders of polymorphonuclear neutrophils
Latin: Dysfunctiones cellularum neutrophilorum polymorphonucleorum
Cell membrane receptor complex [CR3] defect
Chronic (childhood) granulomatous disease
Congenital dysphagocytosis
Progressive septic granulomatosis

D72Other disorders of white blood cells
Latin: Morbi leucocytorum alii
Excludes:basophilia (D75.8)
immunity disorders (D80-D89)
neutropenia (D70)
preleukaemia (syndrome) (D46.9)
D72.0Genetic 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)
D72.1Eosinophilia
Eosinophilia:
· allergic
· hereditary
D72.8Other specified disorders of white blood cells
Leukaemoid reaction:
· lymphocytic
· monocytic
· myelocytic
Leukocytosis
Lymphocytosis (symptomatic)
Lymphopenia
Monocytosis (symptomatic)
Plasmacytosis
D72.9Disorder of white blood cells, unspecified

D73Diseases of spleen
Latin: Morbus splenis
D73.0Hyposplenism
Asplenia, postsurgical
Atrophy of spleen
Excludes:asplenia (congenital) (Q89.0)
D73.1Hypersplenism
Excludes:splenomegaly:
· NOS (R16.1)
· congenital (Q89.0)
D73.2Chronic congestive splenomegaly
D73.3Abscess of spleen
D73.4Cyst of spleen
D73.5Infarction of spleen
Splenic rupture, nontraumatic
Torsion of spleen
Excludes:traumatic rupture of spleen (S36.0)
D73.8Other diseases of spleen
Fibrosis of spleen NOS
Perisplenitis
Splenitis NOS
D73.9Disease of spleen, unspecified

D74Methaemoglobinaemia
Latin: Methaemoglobinaemia
D74.0Congenital methaemoglobinaemia
Congenital NADH-methaemoglobin reductase deficiency
Haemoglobin-M [Hb-M] disease
Methaemoglobinaemia, hereditary
D74.8Other methaemoglobinaemias
Acquired methaemoglobinaemia (with sulfhaemoglobinaemia)
Toxic methaemoglobinaemia
Use additional external cause code (Chapter XX), if desired, to identify cause.
D74.9Methaemoglobinaemia, unspecified

D75Other 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)
D75.0Familial erythrocytosis
Polycythaemia:
· benign
· familial
Excludes:hereditary ovalocytosis (D58.1)
D75.1Secondary 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)
D75.2Essential thrombocytosis
Excludes:essential (haemorrhagic) thrombocythaemia (D47.3)
D75.8Other specified diseases of blood and blood-forming organs
Basophilia
D75.9Disease of blood and blood-forming organs, unspecified

D76Certain 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)
D76.0Langerhans' cell histiocytosis, not elsewhere classified
Eosinophilic granuloma
Hand-Schüller-Christian disease
Histiocytosis X (chronic)
D76.1Haemophagocytic lymphohistiocytosis
Familial haemophagocytic reticulosis
Histiocytoses of mononuclear phagocytes other than Langerhans' cells NOS
D76.2Haemophagocytic syndrome, infection-associated
Use additional code, if desired, to identify infectious agent or disease.
D76.3Other 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.-+)