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| Chapter | Blocks | Title |
|---|---|---|
| I | A00–B99 | Certain infectious and parasitic diseases |
| II | C00–D48 | Neoplasms |
| III | D50–D89 | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism |
| IV | E00–E90 | Endocrine, nutritional and metabolic diseases |
| V | F00–F99 | Mental and behavioural disorders |
| VI | G00–G99 | Diseases of the nervous system |
| VII | H00–H59 | Diseases of the eye and adnexa |
| VIII | H60–H95 | Diseases of the ear and mastoid process |
| IX | I00–I99 | Diseases of the circulatory system |
| X | J00–J99 | Diseases of the respiratory system |
| XI | K00–K93 | Diseases of the digestive system |
| XII | L00–L99 | Diseases of the skin and subcutaneous tissue |
| XIII | M00–M99 | Diseases of the musculoskeletal system and connective tissue |
| XIV | N00–N99 | Diseases of the genitourinary system |
| XV | O00–O99 | Pregnancy, childbirth and the puerperium |
| XVI | P00–P96 | Certain conditions originating in the perinatal period |
| XVII | Q00–Q99 | Congenital malformations, deformations and chromosomal abnormalities |
| XVIII | R00–R99 | Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified |
| XIX | S00–T98 | Injury, poisoning and certain other consequences of external causes |
| XX | V01–Y98 | External causes of morbidity and mortality |
| XXI | Z00–Z99 | Factors influencing health status and contact with health services |
| XXII | U00–U99 | Codes for special purposes |
The International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings, complaints, social circumstances and external causes of injury or diseases, as classified by the World Health Organization (WHO).[1] This page contains ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism.
D50–D89 – Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism [edit]
(D50–D53) Nutritional anemias [edit]
- (D50) Iron deficiency anaemia
- (D50.0) Iron deficiency anaemia secondary to blood loss (chronic)
- (D50.1) Sideropenic dysphagia
- (D50.8) Other iron deficiency anaemias
- (D50.9) Iron deficiency anaemia, unspecified
- (D51) Vitamin B12 deficiency anaemia
- (D51.0) Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
- (D51.1) Vitamin B 12 deficiency anaemia due to selective vitamin B 12 malabsorption with proteinuria
- (D51.2) Transcobalamin II deficiency
- (D51.3) Other dietary vitamin B 12 deficiency anaemia
- (D51.8) Other vitamin B 12 deficiency anaemias
- (D51.9) Vitamin B 12 deficiency anaemia, unspecified
- (D52) Folate deficiency anaemia
- (D53) Other nutritional anaemias
- (D53.0) Protein deficiency anaemia
- (D53.1) Other megaloblastic anaemias, not elsewhere classified
- (D53.2) Scorbutic anaemia
- (D53.8) Other specified nutritional anaemias
- (D53.9) Nutritional anaemia, unspecified
(D55–D59) Haemolytic anaemias [edit]
- (D55) Anaemia due to enzyme disorders
- (D55.0) Anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency
- (D55.1) Anaemia due to other disorders of glutathione metabolism
- (D55.2) Anaemia due to disorders of glycolytic enzymes
- (D55.3) Anaemia due to disorders of nucleotide metabolism
- (D55.8) Other anaemias due to enzyme disorders
- (D55.9) Anaemia due to enzyme disorder, unspecified
- (D56) Thalassaemia
- (D56.0) Alpha thalassaemia
- (D56.1) Beta thalassaemia
- (D56.2) Delta-beta thalassaemia
- (D56.3) Thalassaemia trait
- (D56.4) Hereditary persistence of fetal haemoglobin (HPFH)
- (D56.8) Other thalassaemias
- (D56.9) Thalassaemia, unspecified
- (D57) Sickle-cell disorders
- (D57.0) Sickle-cell anaemia with crisis
- (D57.1) Sickle-cell anaemia without crisis
- (D57.2) Double heterozygous sickling disorders
- (D57.3) Sickle-cell trait
- (D57.8) Other sickle-cell disorders
- (D58) Other hereditary haemolytic anaemias
- (D58.0) Hereditary spherocytosis
- (D58.1) Hereditary elliptocytosis
- Elliptocytosis (congenital)
- Ovalocytosis (congenital)(hereditary)
- (D58.2) Other haemoglobinopathies
- (D58.8) Other specified hereditary haemolytic anaemias
- (D59) Acquired haemolytic anaemia
- (D59.0) Drug-induced autoimmune haemolytic anaemia
- (D59.1) Other autoimmune haemolytic anaemias
- (D59.2) Drug-induce nonautoimmune haemolytic anaemia
- (D59.3) Haemolytic-uraemic syndrome
- (D59.4) Other nonautoimmune haemolytic anaemias
- (D59.5) Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli)
- (D59.6) Haemoglobinuria due to haemolysis from other external causes
- (D59.8) Other acquired haemolytic anaemias
- (D59.9) Acquired haemolytic anaemia, unspecified
(D60–D64) Aplastic and other anaemias [edit]
- (D60) Acquired pure red cell aplasia (erythroblastopenia)
- (D61) Other aplastic anaemias
- (D61.0) Constitutional aplastic anaemia
- (D61.1) Drug-induced aplastic anaemia
- (D61.2) Aplastic anaemia due to other external agents
- (D61.3) Idiopathic aplastic anaemia
- (D61.8) Other specified aplastic anaemias
- (D61.9) Aplastic anaemia, unspecified
- (D62) Acute posthaemorrhagic anaemia
- (D63) Anaemia in chronic diseases classified elsewhere
- (D64) Other anaemias
- (D64.0) Hereditary sideroblastic anaemia
- (D64.1) Secondary sideroblastic anaemia due to disease
- (D64.2) Secondary sideroblastic anaemia due to drugs and toxins
- (D64.3) Other sideroblastic anaemias
- (D64.4) Congenital dyserythropoietic anaemia
- (D64.8) Other specified anaemias
- (D64.9) Anaemia, unspecified
(D65–D69) Coagulation defects, purpura and other haemorrhagic conditions [edit]
- (D65) Disseminated intravascular coagulation (defibrination syndrome)
- Afibrinogenaemia, acquired
- Consumption coagulopathy
- Diffuse or disseminated intravascular coagulation (DIC)
- Fibrinolytic haemorrhage, acquired
- Fibrinolytic purpura
- Purpura fulminans
- (D66) Hereditary factor VIII deficiency
- (D67) Hereditary factor IX deficiency
- (D68) Other coagulation defects
- (D68.0) Von Willebrand's disease
- (D68.1) Hereditary factor XI deficiency
- (D68.2) Hereditary deficiency of other clotting factors
- (D68.3) Haemorrhagic disorder due to circulating anticoagulants
- (D68.4) Acquired coagulation factor deficiency
- (D68.8) Other specified coagulation defects
- (D68.9) Coagulation defect, unspecified
- (D69) Purpura and other haemorrhagic conditions
- (D69.0) Allergic purpura
- (D69.1) Qualitative platelet defects
- Bernard-Soulier syndrome (giant platelet)
- Glanzmann's disease
- Grey platelet syndrome
- Thromboasthenia (haemorrhagic)(hereditary)
- Thrombocytopathy
- (D69.2) Other nonthrombocytopenic purpura
- (D69.3) Idiopathic thrombocytopenic purpura
- (D69.4) Other primary thrombocytopenia
- (D69.5) Secondary thrombocytopenia
- (D69.6) Thrombocytopenia, unspecified
- (D69.8) Other specified haemorrhagic conditions
- (D69.9) Haemorrhagic condition, unspecified
(D70–D77) Other diseases of blood and blood-forming organs [edit]
- (D70) Agranulocytosis
- (D71) Functional disorders of polymorphonuclear neutrophils
- (D72) Other disorders of white blood cells
- (D72.0) Genetic anomalies of leukocytes
- (D72.1) Eosinophilia
- (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
- (D73.1) Hypersplenism
- (D73.2) Chronic congestive splenomegaly
- (D73.3) Abscess of spleen
- (D73.4) Cyst of spleen
- (D73.5) Infarction of spleen
- (D73.8) Other diseases of spleen
- (D73.9) Disease of spleen, unspecified
- (D74) Methaemoglobinaemia
- (D74.0) Congenital methaemoglobinaemia
- Congenital NADH-methaemoglobin reductase deficiency
- Haemoglobin-M (Hb-M) disease
- Methaemoglobinaemia, hereditary
- (D74.8) Other methaemoglobinaemias
- (D74.9) Methaemoglobinaemia, unspecified
- (D74.0) Congenital methaemoglobinaemia
- (D75) Other diseases of blood and blood-forming organs
- (D75.0) Familial erythrocytosis
- (D75.1) Secondary polycythaemia
- (D75.2) Essential thrombocytosis
- (D75.8) Other specified diseases of blood and blood-forming organs
- (D75.9) Disease of blood and blood-forming organs, unspecified
- (D76) Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
- (D76.0) Langerhans' cell histiocytosis, not elsewhere classified
- (D76.1) Haemophagocytic lymphohistiocytosis
- (D76.2) Haemophagocytic syndrome, infection-associated
- (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
(D80–D89) Certain disorders involving the immune mechanism [edit]
- (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
- (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
- (D80.8) Immunodeficiency with predominantly antibody defects, unspecified
- (D80.0) Hereditary hypogammaglobulinaemia
- (D81) Combined immunodeficiencies
- (D81.0) Severe combined immunodeficiency (SCID) with reticular dysgenesis
- (D81.1) Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers
- (D81.2) Severe combined immunodeficiency (SCID) with low or normal B-cell numbers
- (D81.3) Adenosine deaminase deficiency (ADA)
- (D81.4) Nezelof's syndrome
- (D81.5) Purine nucleoside phosphorylase deficiency (PNP)
- (D81.6) Major histocompatibility complex class I deficiency
- (D81.7) Major histocompatibility complex class II deficiency
- (D81.8) Other combined immunodeficiencies
- (D81.9) Combined immunodeficiency, unspecified
- Severe combined immunodeficiency disorder (SCID) NOS
- (D82) Immunodeficiency associated with other major defects
- (D82.0) Wiskott-Aldrich syndrome
- (D82.1) Di George's syndrome
- (D82.2) Immunodeficiency with short-limbed stature
- (D82.3) Immunodeficiency following hereditary defective response to Epstein-Barr virus
- (D82.4) Hyperimmunoglobulin E syndrome (IgE)
- (D83) Common variable immunodeficiency
- (D84) Other immunodeficiencies
- (D84.0) Lymphocyte function antigen-1 (LFA-1) defect
- (D84.1) Defects in the complement system
- (D84.8) Other specified immunodeficiencies
- (D84.9) Immunodeficiency, unspecified
- (D86) Sarcoidosis
- (D86.0) Sarcoidosis of lung
- (D86.1) Sarcoidosis of lymph nodes
- (D86.2) Sarcoidosis of lung with sarcoidosis of lymph nodes
- (D86.3) Sarcoidosis of skin
- (D86.8) Sarcoidosis of other and combined sites
- (D89) Other disorders involving the immune mechanism, not elsewhere classified
- (D89.0) Polyclonal hypergammaglobulinaemia
- (D89.1) Cryoglobulinaemia
- (D89.2) Hypergammaglobulinaemia, unspecified
- (D89.8) Other specified disorders involving the immune mechanism, not elsewhere classified
- (D89.9) Disorder involving the immune mechanism, unspecified
See also [edit]
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
- List of ICD-9 codes 140–239: neoplasms
References [edit]
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