AutoICD API

Chapter 3: Diseases of the Blood and Blood-Forming Organs

ICD-10 to ICD-11 crosswalk mappings for codes D50-D89

192 ICD-10 codes in this chapter have ICD-11 crosswalk mappings from the WHO.

Covers anemia (iron deficiency, sickle cell, aplastic), coagulation disorders including hemophilia and thrombocytopenia, immune deficiencies, and other blood disorders. Iron deficiency anemia (D50) and other anemias are among the most frequently coded conditions in this chapter.

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D50-D53: Nutritional Anemias

23 codes with ICD-11 mappings

D55-D59: Hemolytic Anemias

37 codes with ICD-11 mappings

D55Anemia due to enzyme disorders1 mappingD55.0Anemia due to glucose-6-phosphate dehydrogenase deficiency1 mappingD55.1Anemia due to other disorders of glutathione metabolism1 mappingD55.2Anemia due to disorders of glycolytic enzymes1 mappingD55.3Anemia due to disorders of nucleotide metabolism1 mappingD55.8Other anemias due to enzyme disorders1 mappingD55.9Anemia due to enzyme disorder, unspecified1 mappingD56Thalassemia1 mappingD56.0Alpha thalassemia1 mappingD56.1Beta thalassemia1 mappingD56.2Delta-beta thalassemia1 mappingD56.3Thalassemia minor1 mappingD56.4Hereditary persistence of fetal hemoglobin [HPFH]1 mappingD56.8Other thalassemias1 mappingD56.9Thalassemia, unspecified1 mappingD57Sickle-cell disorders1 mappingD57.0Hb-SS disease with crisis1 mappingD57.1Sickle-cell disease without crisis1 mappingD57.2Sickle-cell/Hb-C disease1 mappingD57.3Sickle-cell trait1 mappingD57.8Other sickle-cell disorders1 mappingD58Other hereditary hemolytic anemias1 mappingD58.0Hereditary spherocytosis1 mappingD58.1Hereditary elliptocytosis1 mappingD58.2Other hemoglobinopathies1 mappingD58.8Other specified hereditary hemolytic anemias1 mappingD58.9Hereditary hemolytic anemia, unspecified1 mappingD59Acquired hemolytic anemia1 mappingD59.0Drug-induced autoimmune hemolytic anemia1 mappingD59.1Other autoimmune hemolytic anemias1 mappingD59.2Drug-induced nonautoimmune hemolytic anemia1 mappingD59.3Hemolytic-uremic syndrome1 mappingD59.4Other nonautoimmune hemolytic anemias1 mappingD59.5Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]1 mappingD59.6Hemoglobinuria due to hemolysis from other external causes1 mappingD59.8Other acquired hemolytic anemias1 mappingD59.9Acquired hemolytic anemia, unspecified1 mapping

D60-D64: Aplastic and Other Anemias and Other Bone Marrow Failure Syndromes

24 codes with ICD-11 mappings

D65-D69: Coagulation Defects, Purpura and Other Hemorrhagic Conditions

23 codes with ICD-11 mappings

D70-D77: Other Disorders of Blood and Blood-Forming Organs

30 codes with ICD-11 mappings

D80-D89: Certain Disorders Involving the Immune Mechanism

55 codes with ICD-11 mappings

D80Immunodeficiency with predominantly antibody defects1 mappingD80.0Hereditary hypogammaglobulinemia1 mappingD80.1Nonfamilial hypogammaglobulinemia1 mappingD80.2Selective deficiency of immunoglobulin A [IgA]1 mappingD80.3Selective deficiency of immunoglobulin G [IgG] subclasses1 mappingD80.4Selective deficiency of immunoglobulin M [IgM]1 mappingD80.5Immunodeficiency with increased immunoglobulin M [IgM]1 mappingD80.6Antibody defic w near-norm immunoglob or w hyperimmunoglob1 mappingD80.7Transient hypogammaglobulinemia of infancy1 mappingD80.8Other immunodeficiencies with predominantly antibody defects1 mappingD80.9Immunodeficiency with predominantly antibody defects, unsp1 mappingD81Combined immunodeficiencies1 mappingD81.0Severe combined immunodeficiency with reticular dysgenesis1 mappingD81.1Severe combined immunodeficiency w low T- and B-cell numbers1 mappingD81.2Severe combined immunodef w low or normal B-cell numbers1 mappingD81.3Adenosine deaminase [ADA] deficiency1 mappingD81.4Nezelof's syndrome1 mappingD81.5Purine nucleoside phosphorylase [PNP] deficiency1 mappingD81.6Major histocompatibility complex class I deficiency1 mappingD81.7Major histocompatibility complex class II deficiency1 mappingD81.8Other combined immunodeficiencies1 mappingD81.9Combined immunodeficiency, unspecified1 mappingD82Immunodeficiency associated with other major defects1 mappingD82.0Wiskott-Aldrich syndrome1 mappingD82.1Di George's syndrome1 mappingD82.2Immunodeficiency with short-limbed stature1 mappingD82.3Immunodef fol heredit defctv response to Epstein-Barr virus1 mappingD82.4Hyperimmunoglobulin E [IgE] syndrome1 mappingD82.8Immunodeficiency associated with oth major defects1 mappingD82.9Immunodeficiency associated with major defect, unspecified1 mappingD83Common variable immunodeficiency1 mappingD83.0Com variab immunodef w predom abnlt of B-cell nums & functn1 mappingD83.1Com variab immunodef w predom immunoreg T-cell disorders1 mappingD83.2Common variable immunodef w autoantibodies to B- or T-cells1 mappingD83.8Other common variable immunodeficiencies1 mappingD83.9Common variable immunodeficiency, unspecified1 mappingD84Other immunodeficiencies1 mappingD84.0Lymphocyte function antigen-1 [LFA-1] defect1 mappingD84.1Defects in the complement system1 mappingD84.8Other specified immunodeficiencies1 mappingD84.9Immunodeficiency, unspecified1 mappingD86Sarcoidosis1 mappingD86.0Sarcoidosis of lung1 mappingD86.1Sarcoidosis of lymph nodes1 mappingD86.2Sarcoidosis of lung with sarcoidosis of lymph nodes1 mappingD86.3Sarcoidosis of skin1 mappingD86.8Sarcoidosis of other sites1 mappingD86.9Sarcoidosis, unspecified1 mappingD89Oth disorders involving the immune mechanism, NEC1 mappingD89.0Polyclonal hypergammaglobulinemia1 mappingD89.1Cryoglobulinemia1 mappingD89.2Hypergammaglobulinemia, unspecified1 mappingD89.3Immune reconstitution syndrome1 mappingD89.8Oth disrd involving the immune mechanism, NEC1 mappingD89.9Disorder involving the immune mechanism, unspecified1 mapping