ICD-10 Chapter III



Coding system
ICD-10
Organisation
OpenSAFELY
Codelist ID
opensafely/icd-10-chapter-iii
ID
5ec57aee

Versions
  • 5ec57aee

No metadata has been provided for this codelist.

code term
D50 Iron deficiency anaemia
D50-D53 Nutritional anaemias
D500 Iron deficiency anaemia secondary to blood loss (chronic)
D501 Sideropenic dysphagia
D508 Other iron deficiency anaemias
D509 Iron deficiency anaemia, unspecified
D51 Vitamin B 12 deficiency anaemia
D510 Vitamin B 12 deficiency anaemia due to intrinsic factor deficiency
D511 Vitamin B 12 deficiency anaemia due to selective vitamin B 12 malabsorption with proteinuria
D512 Transcobalamin II deficiency
D513 Other dietary vitamin B 12 deficiency anaemia
D518 Other vitamin B 12 deficiency anaemias
D519 Vitamin B 12 deficiency anaemia, unspecified
D52 Folate deficiency anaemia
D520 Dietary folate deficiency anaemia
D521 Drug-induced folate deficiency anaemia
D528 Other folate deficiency anaemias
D529 Folate deficiency anaemia, unspecified
D53 Other nutritional anaemias
D530 Protein deficiency anaemia
D531 Other megaloblastic anaemias, not elsewhere classified
D532 Scorbutic anaemia
D538 Other specified nutritional anaemias
D539 Nutritional anaemia, unspecified
D55 Anaemia due to enzyme disorders
D55-D59 Haemolytic anaemias
D550 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551 Anaemia due to other disorders of glutathione metabolism
D552 Anaemia due to disorders of glycolytic enzymes
D553 Anaemia due to disorders of nucleotide metabolism
D558 Other anaemias due to enzyme disorders
D559 Anaemia due to enzyme disorder, unspecified
D56 Thalassaemia
D560 Alpha thalassaemia
D561 Beta thalassaemia
D562 Delta-beta thalassaemia
D563 Thalassaemia trait
D564 Hereditary persistence of fetal haemoglobin [HPFH]
D568 Other thalassaemias
D569 Thalassaemia, unspecified
D57 Sickle-cell disorders
D570 Sickle-cell anaemia with crisis
D571 Sickle-cell anaemia without crisis
D572 Double heterozygous sickling disorders
D573 Sickle-cell trait
D578 Other sickle-cell disorders
D58 Other hereditary haemolytic anaemias
D580 Hereditary spherocytosis
D581 Hereditary elliptocytosis
D582 Other haemoglobinopathies
D588 Other specified hereditary haemolytic anaemias
D589 Hereditary haemolytic anaemia, unspecified
D59 Acquired haemolytic anaemia
D590 Drug-induced autoimmune haemolytic anaemia
D591 Other autoimmune haemolytic anaemias
D592 Drug-induced nonautoimmune haemolytic anaemia
D593 Haemolytic-uraemic syndrome
D594 Other nonautoimmune haemolytic anaemias
D595 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
D596 Haemoglobinuria due to haemolysis from other external causes
D598 Other acquired haemolytic anaemias
D599 Acquired haemolytic anaemia, unspecified
D60 Acquired pure red cell aplasia [erythroblastopenia]
D60-D64 Aplastic and other anaemias
D600 Chronic acquired pure red cell aplasia
D601 Transient acquired pure red cell aplasia
D608 Other acquired pure red cell aplasias
D609 Acquired pure red cell aplasia, unspecified
D61 Other aplastic anaemias
D610 Constitutional aplastic anaemia
D611 Drug-induced aplastic anaemia
D612 Aplastic anaemia due to other external agents
D613 Idiopathic aplastic anaemia
D618 Other specified aplastic anaemias
D619 Aplastic anaemia, unspecified
D62 Acute posthaemorrhagic anaemia
D63 Anaemia in chronic diseases classified elsewhere
D630 Anaemia in neoplastic disease C00-D48
D638 Anaemia in other chronic diseases classified elsewhere
D64 Other anaemias
D640 Hereditary sideroblastic anaemia
D641 Secondary sideroblastic anaemia due to disease
D642 Secondary sideroblastic anaemia due to drugs and toxins
D643 Other sideroblastic anaemias
D644 Congenital dyserythropoietic anaemia
D648 Other specified anaemias
D649 Anaemia, unspecified
D65 Disseminated intravascular coagulation [defibrination syndrome]
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions
D66 Hereditary factor VIII deficiency
D67 Hereditary factor IX deficiency
D68 Other coagulation defects
D680 Von Willebrand disease
D681 Hereditary factor XI deficiency
D682 Hereditary deficiency of other clotting factors
D683 Haemorrhagic disorder due to circulating anticoagulants
D684 Acquired coagulation factor deficiency
D685 Primary thrombophilia
D686 Other thrombophilia
D688 Other specified coagulation defects
D689 Coagulation defect, unspecified
D69 Purpura and other haemorrhagic conditions
D690 Allergic purpura
D691 Qualitative platelet defects
D692 Other nonthrombocytopenic purpura
D693 Idiopathic thrombocytopenic purpura
D694 Other primary thrombocytopenia
D695 Secondary thrombocytopenia
D696 Thrombocytopenia, unspecified
D698 Other specified haemorrhagic conditions
D699 Haemorrhagic condition, unspecified
D70 Agranulocytosis
D70-D77 Other diseases of blood and blood-forming organs
D71 Functional disorders of polymorphonuclear neutrophils
D72 Other disorders of white blood cells
D720 Genetic anomalies of leukocytes
D721 Eosinophilia
D728 Other specified disorders of white blood cells
D729 Disorder of white blood cells, unspecified
D73 Diseases of spleen
D730 Hyposplenism
D731 Hypersplenism
D732 Chronic congestive splenomegaly
D733 Abscess of spleen
D734 Cyst of spleen
D735 Infarction of spleen
D738 Other diseases of spleen
D739 Disease of spleen, unspecified
D74 Methaemoglobinaemia
D740 Congenital methaemoglobinaemia
D748 Other methaemoglobinaemias
D749 Methaemoglobinaemia, unspecified
D75 Other diseases of blood and blood-forming organs
D750 Familial erythrocytosis
D751 Secondary polycythaemia
D758 Other specified diseases of blood and blood-forming organs
D759 Disease of blood and blood-forming organs, unspecified
D76 Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue
D761 Haemophagocytic lymphohistiocytosis
D762 Haemophagocytic syndrome, infection-associated
D763 Other histiocytosis syndromes
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
D80 Immunodeficiency with predominantly antibody defects
D80-D89 Certain disorders involving the immune mechanism
D800 Hereditary hypogammaglobulinaemia
D801 Nonfamilial hypogammaglobulinaemia
D802 Selective deficiency of immunoglobulin A [IgA]
D803 Selective deficiency of immunoglobulin G [IgG] subclasses
D804 Selective deficiency of immunoglobulin M [IgM]
D805 Immunodeficiency with increased immunoglobulin M [IgM]
D806 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
D807 Transient hypogammaglobulinaemia of infancy
D808 Other immunodeficiencies with predominantly antibody defects
D809 Immunodeficiency with predominantly antibody defects, unspecified
D81 Combined immunodeficiencies
D810 Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D813 Adenosine deaminase [ADA] deficiency
D814 Nezelof syndrome
D815 Purine nucleoside phosphorylase [PNP] deficiency
D816 Major histocompatibility complex class I deficiency
D817 Major histocompatibility complex class II deficiency
D818 Other combined immunodeficiencies
D819 Combined immunodeficiency, unspecified
D82 Immunodeficiency associated with other major defects
D820 Wiskott-Aldrich syndrome
D821 Di George syndrome
D822 Immunodeficiency with short-limbed stature
D823 Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824 Hyperimmunoglobulin E [IgE] syndrome
D828 Immunodeficiency associated with other specified major defects
D829 Immunodeficiency associated with major defect, unspecified
D83 Common variable immunodeficiency
D830 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832 Common variable immunodeficiency with autoantibodies to B- or T-cells
D838 Other common variable immunodeficiencies
D839 Common variable immunodeficiency, unspecified
D84 Other immunodeficiencies
D840 Lymphocyte function antigen-1 [LFA-1] defect
D841 Defects in the complement system
D848 Other specified immunodeficiencies
D849 Immunodeficiency, unspecified
D86 Sarcoidosis
D860 Sarcoidosis of lung
D861 Sarcoidosis of lymph nodes
D862 Sarcoidosis of lung with sarcoidosis of lymph nodes
D863 Sarcoidosis of skin
D868 Sarcoidosis of other and combined sites
D869 Sarcoidosis, unspecified
D89 Other disorders involving the immune mechanism, not elsewhere classified
D890 Polyclonal hypergammaglobulinaemia
D891 Cryoglobulinaemia
D892 Hypergammaglobulinaemia, unspecified
D893 Immune reconstitution syndrome
D898 Other specified disorders involving the immune mechanism, not elsewhere classified
D899 Disorder involving the immune mechanism, unspecified
III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Codes not in the full codelist are in faint grey.