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

ICD-10 Chapter III

• 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

• D61818 Other pancytopenia

• D6182 Myelophthisis

• 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

• D68311 Acquired hemophilia

• 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

• D6941 Evans syndrome

• 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

• D721 Eosinophilia

• D72810 Lymphocytopenia

• D72818 Other decreased white blood cell count

• D72819 Decreased white blood cell count, unspecified

• D72820 Lymphocytosis (symptomatic)

• D72821 Monocytosis (symptomatic)

• D72822 Plasmacytosis

• D72823 Leukemoid reaction

• D72824 Basophilia

• D72825 Bandemia

• 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

• D730 Hyposplenism

• D731 Hypersplenism

• D732 Chronic congestive splenomegaly

• D733 Abscess of spleen

• D734 Cyst 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

• D7581 Myelofibrosis

• 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

• D81810 Biotinidase 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

• D8681 Sarcoid meningitis

• D8682 Multiple cranial nerve palsies in sarcoidosis

• D8683 Sarcoid iridocyclitis

• D8684 Sarcoid pyelonephritis

• D8685 Sarcoid myocarditis

• D8686 Sarcoid arthropathy

• D8687 Sarcoid myositis

• 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