C00-D48 - Neoplasms

D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

(D50-D53) Nutritional anemias

• Iron deficiency anaemia
• Iron deficiency anaemia secondary to blood loss (chronic)
• Sideropenic dysphagia
• Kelly-Paterson syndrome
• Plummer-Vinson syndrome
• Other iron deficiency anaemias
• Iron deficiency anaemia, unspecified

• Vitamin B12 deficiency anaemia
• Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
• Pernicious anemia
• Vitamin B 12 deficiency anaemia due to selective vitamin B 12 malabsorption with proteinuria
• Megaloblastic hereditary anaemia
• Transcobalamin II deficiency
• Other dietary vitamin B 12 deficiency anaemia
• Other vitamin B 12 deficiency anaemias
• Vitamin B 12 deficiency anaemia, unspecified

• Folate deficiency anaemia
• Dietary folate deficiency anaemia
• Nutritional megaloblastic anaemia
• Drug-induced folate deficiency anaemia
• Other folate deficiency anaemias
• Folate deficiency anaemia, unspecified

• Other nutritional anaemias
• Protein deficiency anaemia
• Other megaloblastic anaemias, not elsewhere classified
• Scorbutic anaemia
• Other specified nutritional anaemias
• Nutritional anaemia, unspecified

(D55-D59) Haemolytic anaemias

• Anaemia due to enzyme disorders
• Anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency
• Favism
• G6PD deficiency anaemia
• Anaemia due to other disorders of glutathione metabolism
• Anaemia due to disorders of glycolytic enzymes
• hexokinase deficiency
• pyruvate kinase deficiency
• triose-phosphate isomerase deficiency
• Anaemia due to disorders of nucleotide metabolism
• Other anaemias due to enzyme disorders
• Anaemia due to enzyme disorder, unspecified

• Thalassaemia
• Alpha thalassaemia
• Beta thalassaemia
• Delta-beta thalassaemia
• Thalassaemia trait
• Hereditary persistence of fetal haemoglobin (HPFH)
• Other thalassaemias
• Thalassaemia, unspecified

• Sickle-cell disorders
• Sickle-cell anaemia with crisis
• Sickle-cell anaemia without crisis
• Double heterozygous sickling disorders
• Sickle-cell trait
• Other sickle-cell disorders

• Other hereditary haemolytic anaemias
• Hereditary spherocytosis
• Acholuric (familial) jaundice
• Congenital (spherocytic) haemolytic icterus
• Minkowski-Chauffard syndrome
• Hereditary elliptocytosis
• Elliptocytosis (congenital)
• Ovalocytosis (congenital)(hereditary)
• Other haemoglobinopathies
• Abnormal haemoglobin NOS
• Congenital Heinz body anaemia
• Haemoglobinopathy NOS
• Unstable haemoglobin haemolytic disease
• Other specified hereditary haemolytic anaemias
• Stomatocytosis

• Acquired haemolytic anaemia
• Drug-induced autoimmune haemolytic anaemia
• Other autoimmune haemolytic anaemias
• Warm autoimmune hemolytic anemia
• Drug-induced nonautoimmune haemolytic anaemia
• Haemolytic-uraemic syndrome
• Other nonautoimmune haemolytic anaemias
• Microangiopathic hemolytic anemia
• Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli)
• Haemoglobinuria due to haemolysis from other external causes
• paroxysmal cold haemoglobinuria
• Other acquired haemolytic anaemias
• Acquired haemolytic anaemia, unspecified

(D60-D64) Aplastic and other anaemias

• Acquired pure red cell aplasia (erythroblastopenia)
• Other aplastic anaemias
• Constitutional aplastic anaemia
• Fanconi anemia
• Acute posthaemorrhagic anaemia
• Anaemia in chronic diseases classified elsewhere
• Other anaemias
• Hereditary sideroblastic anaemia
• Secondary sideroblastic anaemia due to disease
• Secondary sideroblastic anaemia due to drugs and toxins
• Other sideroblastic anaemias
• Congenital dyserythropoietic anaemia
• Other specified anaemias
• Anaemia, unspecified

(D65-D69) Coagulation defects, purpura and other haemorrhagic conditions

• Disseminated intravascular coagulation (defibrination syndrome)
• Afibrinogenaemia, acquired
• Consumption coagulopathy
• Diffuse or disseminated intravascular coagulation (DIC)
• Fibrinolytic haemorrhage, acquired
• Fibrinolytic purpura
• Purpura fulminans

• Hereditary factor VIII deficiency
• Haemophilia A

• Hereditary factor IX deficiency
• Christmas disease

• Other coagulation defects
• Von Willebrand's disease
• Hereditary factor XI deficiency
• Haemophilia C
• Hereditary deficiency of other clotting factors
• Haemorrhagic disorder due to circulating anticoagulants
• Acquired coagulation factor deficiency
• Other specified coagulation defects
• Coagulation defect, unspecified

• Purpura and other haemorrhagic conditions
• Allergic purpura
• anaphylactoid purpura
• Henoch-Schönlein purpura
• Qualitative platelet defects
• Bernard-Soulier syndrome (giant platelet)
• Glanzmann's disease
• Grey platelet syndrome
• Thromboasthenia (haemorrhagic)(hereditary)
• Thrombocytopathy
• Other nonthrombocytopenic purpura
• Idiopathic thrombocytopenic purpura
• Evans' syndrome
• Other primary thrombocytopenia
• Secondary thrombocytopenia
• Thrombocytopenia, unspecified
• Other specified haemorrhagic conditions
• Haemorrhagic condition, unspecified

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

• Agranulocytosis
• Agranulocytic angina
• Infantile genetic agranulocytosis
• Kostmann's disease
• Neutropenia, NOS

• Functional disorders of polymorphonuclear neutrophils
• Cell membrane receptor complex (CR3) defect
• Chronic (childhood) granulomatous disease
• Congenital dysphagocytosis
• Progressive septic granulomatosis

• Other disorders of white blood cells
• Genetic anomalies of leukocytes
• Alder anomaly
• May-Hegglin anomaly
• Pelger-Huët anomaly
• Eosinophilia
• Other specified disorders of white blood cells
• Leukaemoid reaction: lymphocytic, monocytic, myelocytic
• Leukocytosis
• Lymphocytosis (symptomatic)
• Lymphopenia
• Monocytosis (symptomatic)
• Plasmacytosis
• Disorder of white blood cells, unspecified

• Diseases of spleen
• Hyposplenism
• Hypersplenism
• Chronic congestive splenomegaly
• Abscess of spleen
• Cyst of spleen
• Infarction of spleen
• Other diseases of spleen
• Disease of spleen, unspecified

• Methaemoglobinaemia
• Congenital methaemoglobinaemia
• Congenital NADH-methaemoglobin reductase deficiency
• Haemoglobin-M (Hb-M) disease
• Methaemoglobinaemia, hereditary
• Other methaemoglobinaemias
• Acquired methaemoglobinaemia (with sulfhaemoglobinaemia)
• Toxic methaemoglobinaemia
• Methaemoglobinaemia, unspecified

• Other diseases of blood and blood-forming organs
• Familial erythrocytosis
• Secondary polycythaemia
• Essential thrombocytosis
• Other specified diseases of blood and blood-forming organs
• Basophilia
• Disease of blood and blood-forming organs, unspecified

• Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
• Langerhans' cell histiocytosis, not elsewhere classified
• Eosinophilic granuloma
• Hand-Schüller-Christian disease
• Histiocytosis X (chronic)
• Haemophagocytic lymphohistiocytosis
• Familial haemophagocytic reticulosis
• Haemophagocytic syndrome, infection-associated
• Other histiocytosis syndromes
• Reticulohistiocytoma (giant-cell)
• Sinus histiocytosis with massive lymphadenopathy
• Xanthogranuloma

• Other disorders of blood and blood-forming organs in diseases classified elsewhere

(D80-D89) Certain disorders involving the immune mechanism

• Immunodeficiency with predominantly antibody defects
• Hereditary hypogammaglobulinaemia
• Autosomal recessive agammaglobulinaemia (Swiss type)
• X-linked agammaglobulinaemia (Bruton) (with growth hormone deficiency)
• Nonfamilial hypogammaglobulinaemia
• Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes
• Common variable agammaglobulinaemia (CVAgamma)
• Hypogammaglobulinaemia NOS
• Selective deficiency of immunoglobulin A (IgA)
• Selective deficiency of immunoglobulin G (IgG) subclasses
• Selective deficiency of immunoglobulin M (IgM)
• Immunodeficiency with increased immunoglobulin M (IgM)
• Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
• Transient hypogammaglobulinaemia of infancy
• Other immunodeficiencies with predominantly antibody defects
• Kappa light chain deficiency
• Immunodeficiency with predominantly antibody defects, unspecified

• Combined immunodeficiencies
• Severe combined immunodeficiency (SCID) with reticular dysgenesis
• Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers
• Severe combined immunodeficiency (SCID) with low or normal B-cell numbers
• Adenosine deaminase deficiency (ADA)
• Nezelof's syndrome
• Purine nucleoside phosphorylase deficiency (PNP)
• Major histocompatibility complex class I deficiency
• Bare lymphocyte syndrome
• Major histocompatibility complex class II deficiency
• Other combined immunodeficiencies
• Biotin-dependent carboxylase deficiency
• Combined immunodeficiency, unspecified
• Severe combined immunodeficiency disorder (SCID) NOS

• Immunodeficiency associated with other major defects
• Wiskott-Aldrich syndrome
• Immunodeficiency with thrombocytopenia and eczema
• Di George's syndrome
• Immunodeficiency with short-limbed stature
• Immunodeficiency following hereditary defective response to Epstein-Barr virus
• X-linked lymphoproliferative disease
• Hyperimmunoglobulin E syndrome (IgE)
• Common variable immunodeficiency
• Other immunodeficiencies
• Lymphocyte function antigen-1 (LFA-1) defect
• Defects in the complement system
• C1 esterase inhibitor deficiency (C1-INH)
• Other specified immunodeficiencies
• Immunodeficiency, unspecified

• Sarcoidosis
• Sarcoidosis of lung
• Sarcoidosis of lymph nodes
• Sarcoidosis of lung with sarcoidosis of lymph nodes
• Sarcoidosis of skin
• Sarcoidosis of other and combined sites
• Other disorders involving the immune mechanism, not elsewhere classified
• Polyclonal hypergammaglobulinaemia
• Benign hypergammaglobulinaemic purpura
• Polyclonal gammopathy NOS
• Cryoglobulinaemia
• Hypergammaglobulinaemia, unspecified
• Other specified disorders involving the immune mechanism, not elsewhere classified
• Disorder involving the immune mechanism, unspecified

See also

• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems
• List of ICD-9 codes 140-239: Neoplasms