ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism

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ICD-10 Chapter III

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ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism is an international classification of diseases, version 10 ICD-10 diagnostic codes.

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Resources for ICD-10 Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism

Medical classification


  • D500 Iron deficiency anemia secondary to blood loss (chronic)
  • D501 Sideropenic dysphagia
  • D508 Other iron deficiency anemias
  • D509 Iron deficiency anemia, unspecified
  • D510 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
  • D511 Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
  • D512 Transcobalamin II deficiency
  • D513 Other dietary vitamin B12 deficiency anemia
  • D518 Other vitamin B12 deficiency anemias
  • D519 Vitamin B12 deficiency anemia, unspecified
  • D520 Dietary folate deficiency anemia
  • D521 Drug-induced folate deficiency anemia
  • D528 Other folate deficiency anemias
  • D529 Folate deficiency anemia, unspecified
  • D530 Protein deficiency anemia
  • D531 Other megaloblastic anemias, not elsewhere classified
  • D532 Scorbutic anemia
  • D538 Other specified nutritional anemias
  • D539 Nutritional anemia, unspecified
  • D550 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
  • D551 Anemia due to other disorders of glutathione metabolism
  • D552 Anemia due to disorders of glycolytic enzymes
  • D553 Anemia due to disorders of nucleotide metabolism
  • D558 Other anemias due to enzyme disorders
  • D559 Anemia due to enzyme disorder, unspecified
  • D560 Alpha thalassemia
  • D561 Beta thalassemia
  • D562 Delta-beta thalassemia
  • D563 Thalassemia minor
  • D564 Hereditary persistence of fetal hemoglobin [HPFH]
  • D565 Hemoglobin E-beta thalassemia
  • D568 Other thalassemias
  • D569 Thalassemia, unspecified
  • D5700 Hb-SS disease with crisis, unspecified
  • D5701 Hb-SS disease with acute chest syndrome
  • D5702 Hb-SS disease with splenic sequestration
  • D571 Sickle-cell disease without crisis
  • D5720 Sickle-cell/Hb-C disease without crisis
  • D57211 Sickle-cell/Hb-C disease with acute chest syndrome
  • D57212 Sickle-cell/Hb-C disease with splenic sequestration
  • D57219 Sickle-cell/Hb-C disease with crisis, unspecified
  • D573 Sickle-cell trait
  • D5740 Sickle-cell thalassemia without crisis
  • D57411 Sickle-cell thalassemia with acute chest syndrome
  • D57412 Sickle-cell thalassemia with splenic sequestration
  • D57419 Sickle-cell thalassemia with crisis, unspecified
  • D5780 Other sickle-cell disorders without crisis
  • D57811 Other sickle-cell disorders with acute chest syndrome
  • D57812 Other sickle-cell disorders with splenic sequestration
  • D57819 Other sickle-cell disorders with crisis, unspecified
  • D580 Hereditary spherocytosis
  • D581 Hereditary elliptocytosis
  • D582 Other hemoglobinopathies
  • D588 Other specified hereditary hemolytic anemias
  • D589 Hereditary hemolytic anemia, unspecified
  • D590 Drug-induced autoimmune hemolytic anemia
  • D591 Other autoimmune hemolytic anemias
  • D592 Drug-induced nonautoimmune hemolytic anemia
  • D593 Hemolytic-uremic syndrome
  • D594 Other nonautoimmune hemolytic anemias
  • D595 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
  • D596 Hemoglobinuria due to hemolysis from other external causes
  • D598 Other acquired hemolytic anemias
  • D599 Acquired hemolytic anemia, unspecified
  • 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
  • D6101 Constitutional (pure) red blood cell aplasia
  • D6109 Other constitutional aplastic anemia
  • D611 Drug-induced aplastic anemia
  • D612 Aplastic anemia due to other external agents
  • D613 Idiopathic aplastic anemia
  • D61810 Antineoplastic chemotherapy induced pancytopenia
  • D61811 Other drug-induced pancytopenia
  • D6189 Other specified aplastic anemias and other bone marrow failure syndromes
  • D619 Aplastic anemia, unspecified
  • D62 Acute posthemorrhagic anemia
  • D630 Anemia in neoplastic disease
  • D631 Anemia in chronic kidney disease
  • D638 Anemia in other chronic diseases classified elsewhere
  • D640 Hereditary sideroblastic anemia
  • D641 Secondary sideroblastic anemia due to disease
  • D642 Secondary sideroblastic anemia due to drugs and toxins
  • D643 Other sideroblastic anemias
  • D644 Congenital dyserythropoietic anemia
  • D6481 Anemia due to antineoplastic chemotherapy
  • D6489 Other specified anemias
  • D649 Anemia, unspecified
  • D65 Disseminated intravascular coagulation [defibrination syndrome]
  • D66 Hereditary factor VIII deficiency
  • D67 Hereditary factor IX deficiency
  • D680 Von Willebrand's disease
  • D681 Hereditary factor XI deficiency
  • D682 Hereditary deficiency of other clotting factors
  • D68312 Antiphospholipid antibody with hemorrhagic disorder
  • D68318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
  • D6832 Hemorrhagic disorder due to extrinsic circulating anticoagulants
  • D684 Acquired coagulation factor deficiency
  • D6851 Activated protein C resistance
  • D6852 Prothrombin gene mutation
  • D6859 Other primary thrombophilia
  • D6861 Antiphospholipid syndrome
  • D6862 Lupus anticoagulant syndrome
  • D6869 Other thrombophilia
  • D688 Other specified coagulation defects
  • D689 Coagulation defect, unspecified
  • D690 Allergic purpura
  • D691 Qualitative platelet defects
  • D692 Other nonthrombocytopenic purpura
  • D693 Immune thrombocytopenic purpura
  • D6942 Congenital and hereditary thrombocytopenia purpura
  • D6949 Other primary thrombocytopenia
  • D6951 Posttransfusion purpura
  • D6959 Other secondary thrombocytopenia
  • D696 Thrombocytopenia, unspecified
  • D698 Other specified hemorrhagic conditions
  • D699 Hemorrhagic condition, unspecified
  • D700 Congenital agranulocytosis
  • D701 Agranulocytosis secondary to cancer chemotherapy
  • D702 Other drug-induced agranulocytosis
  • D703 Neutropenia due to infection
  • D704 Cyclic neutropenia
  • D708 Other neutropenia
  • D709 Neutropenia, unspecified
  • D71 Functional disorders of polymorphonuclear neutrophils
  • D720 Genetic anomalies of leukocytes
  • D72818 Other decreased white blood cell count
  • D72819 Decreased white blood cell count, unspecified
  • D72820 Lymphocytosis (symptomatic)
  • D72821 Monocytosis (symptomatic)
  • D72828 Other elevated white blood cell count
  • D72829 Elevated white blood cell count, unspecified
  • D7289 Other specified disorders of white blood cells
  • D729 Disorder of white blood cells, unspecified
  • D732 Chronic congestive splenomegaly
  • D733 Abscess of spleen
  • D735 Infarction of spleen
  • D7381 Neutropenic splenomegaly
  • D7389 Other diseases of spleen
  • D739 Disease of spleen, unspecified
  • D740 Congenital methemoglobinemia
  • D748 Other methemoglobinemias
  • D749 Methemoglobinemia, unspecified
  • D750 Familial erythrocytosis
  • D751 Secondary polycythemia
  • D7582 Heparin induced thrombocytopenia (HIT)
  • D7589 Other specified diseases of blood and blood-forming organs
  • D759 Disease of blood and blood-forming organs, unspecified
  • D761 Hemophagocytic lymphohistiocytosis
  • D762 Hemophagocytic syndrome, infection-associated
  • D763 Other histiocytosis syndromes
  • D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
  • D7801 Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
  • D7802 Intraoperative hemorrhage and hematoma of the spleen complicating other procedure
  • D7811 Accidental puncture and laceration of the spleen during a procedure on the spleen
  • D7812 Accidental puncture and laceration of the spleen during other procedure
  • D7821 Postprocedural hemorrhage of the spleen following a procedure on the spleen
  • D7822 Postprocedural hemorrhage of the spleen following other procedure
  • D7831 Postprocedural hematoma of the spleen following a procedure on the spleen
  • D7832 Postprocedural hematoma of the spleen following other procedure
  • D7833 Postprocedural seroma of the spleen following a procedure on the spleen
  • D7834 Postprocedural seroma of the spleen following other procedure
  • D7881 Other intraoperative complications of the spleen
  • D7889 Other postprocedural complications of the spleen
  • D800 Hereditary hypogammaglobulinemia
  • D801 Nonfamilial hypogammaglobulinemia
  • 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 hyperimmunoglobulinemia
  • D807 Transient hypogammaglobulinemia of infancy
  • D808 Other immunodeficiencies with predominantly antibody defects
  • D809 Immunodeficiency with predominantly antibody defects, unspecified
  • 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's syndrome
  • D815 Purine nucleoside phosphorylase [PNP] deficiency
  • D816 Major histocompatibility complex class I deficiency
  • D817 Major histocompatibility complex class II deficiency
  • D81818 Other biotin-dependent carboxylase deficiency
  • D81819 Biotin-dependent carboxylase deficiency, unspecified
  • D8189 Other combined immunodeficiencies
  • D819 Combined immunodeficiency, unspecified
  • D820 Wiskott-Aldrich syndrome
  • D821 Di George's 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
  • 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
  • D840 Lymphocyte function antigen-1 [LFA-1] defect
  • D841 Defects in the complement system
  • D848 Other specified immunodeficiencies
  • D849 Immunodeficiency, unspecified
  • D860 Sarcoidosis of lung
  • D861 Sarcoidosis of lymph nodes
  • D862 Sarcoidosis of lung with sarcoidosis of lymph nodes
  • D863 Sarcoidosis of skin
  • D8682 Multiple cranial nerve palsies in sarcoidosis
  • D8683 Sarcoid iridocyclitis
  • D8684 Sarcoid pyelonephritis
  • D8685 Sarcoid myocarditis
  • D8686 Sarcoid arthropathy
  • D8689 Sarcoidosis of other sites
  • D869 Sarcoidosis, unspecified
  • D890 Polyclonal hypergammaglobulinemia
  • D891 Cryoglobulinemia
  • D892 Hypergammaglobulinemia, unspecified
  • D893 Immune reconstitution syndrome
  • D8940 Mast cell activation, unspecified
  • D8941 Monoclonal mast cell activation syndrome
  • D8942 Idiopathic mast cell activation syndrome
  • D8943 Secondary mast cell activation
  • D8949 Other mast cell activation disorder
  • D89810 Acute graft-versus-host disease
  • D89811 Chronic graft-versus-host disease
  • D89812 Acute on chronic graft-versus-host disease
  • D89813 Graft-versus-host disease, unspecified
  • D8982 Autoimmune lymphoproliferative syndrome [ALPS]
  • D8989 Other specified disorders involving the immune mechanism, not elsewhere classified
  • D899 Disorder involving the immune mechanism, unspecified
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