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.