ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual
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DRAFT
ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual |
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| MDC 16 Diseases and disorders of blood, blood forming organs and immunologic disorders |
| Assignment of Diagnosis Codes |
| A182 | Tuberculous peripheral lymphadenopathy |
| A1885 | Tuberculosis of spleen |
| A281 | Cat-scratch disease |
| D150 | Benign neoplasm of thymus |
| D181 | Lymphangioma, any site |
| D360 | Benign neoplasm of lymph nodes |
| D3A091 | Benign carcinoid tumor of the thymus |
| D460 | Refractory anemia without ring sideroblasts, so stated |
| D461 | Refractory anemia with ring sideroblasts |
| D4620 | Refractory anemia with excess of blasts, unspecified |
| D4621 | Refractory anemia with excess of blasts 1 |
| D4622 | Refractory anemia with excess of blasts 2 |
| D464 | Refractory anemia, unspecified |
| D469 | Myelodysplastic syndrome, unspecified |
| D46A | Refractory cytopenia with multilineage dysplasia |
| D46B | Refractory cytopenia with multilineage dysplasia and ring sideroblasts |
| D46C | Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality |
| D46Z | Other myelodysplastic syndromes |
| D472 | Monoclonal gammopathy |
| D473 | Essential (hemorrhagic) thrombocythemia |
| D474 | Osteomyelofibrosis |
| 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 |
| D5521 | Anemia due to pyruvate kinase deficiency |
| D5529 | Anemia due to other 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 |
| D5703 | Hb-SS disease with cerebral vascular involvement |
| D5709 | Hb-SS disease with crisis with other specified complication |
| 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 |
| D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
| D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
| D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
| D573 | Sickle-cell trait |
| D5740 | Sickle-cell thalassemia without crisis |
| D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
| D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
| D57413 | Sickle-cell thalassemia, unspecified, with cerebral vascular involvement |
| D57418 | Sickle-cell thalassemia, unspecified, with crisis with other specified complication |
| D57419 | Sickle-cell thalassemia, unspecified, with crisis |
| D5742 | Sickle-cell thalassemia beta zero without crisis |
| D57431 | Sickle-cell thalassemia beta zero with acute chest syndrome |
| D57432 | Sickle-cell thalassemia beta zero with splenic sequestration |
| D57433 | Sickle-cell thalassemia beta zero with cerebral vascular involvement |
| D57438 | Sickle-cell thalassemia beta zero with crisis with other specified complication |
| D57439 | Sickle-cell thalassemia beta zero with crisis, unspecified |
| D5744 | Sickle-cell thalassemia beta plus without crisis |
| D57451 | Sickle-cell thalassemia beta plus with acute chest syndrome |
| D57452 | Sickle-cell thalassemia beta plus with splenic sequestration |
| D57453 | Sickle-cell thalassemia beta plus with cerebral vascular involvement |
| D57458 | Sickle-cell thalassemia beta plus with crisis with other specified complication |
| D57459 | Sickle-cell thalassemia beta plus 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 |
| D57813 | Other sickle-cell disorders with cerebral vascular involvement |
| D57818 | Other sickle-cell disorders with crisis with other specified complication |
| 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 |
| D5910 | Autoimmune hemolytic anemia, unspecified |
| D5911 | Warm autoimmune hemolytic anemia |
| D5912 | Cold autoimmune hemolytic anemia |
| D5913 | Mixed type autoimmune hemolytic anemia |
| D5919 | Other autoimmune hemolytic anemia |
| D592 | Drug-induced nonautoimmune hemolytic anemia |
| D5930 | Hemolytic-uremic syndrome, unspecified |
| D5931 | Infection-associated hemolytic-uremic syndrome |
| D5932 | Hereditary hemolytic-uremic syndrome |
| D5939 | Other 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 |
| 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 |
| D6800 | Von Willebrand disease, unspecified |
| D6801 | Von Willebrand disease, type 1 |
| D68020 | Von Willebrand disease, type 2A |
| D68021 | Von Willebrand disease, type 2B |
| D68022 | Von Willebrand disease, type 2M |
| D68023 | Von Willebrand disease, type 2N |
| D68029 | Von Willebrand disease, type 2, unspecified |
| D6803 | Von Willebrand disease, type 3 |
| D6804 | Acquired von Willebrand disease |
| D6809 | Other von Willebrand 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 |
| D7210 | Eosinophilia, unspecified |
| D72110 | Idiopathic hypereosinophilic syndrome [IHES] |
| D72111 | Lymphocytic Variant Hypereosinophilic Syndrome [LHES] |
| D72118 | Other hypereosinophilic syndrome |
| D72119 | Hypereosinophilic syndrome [HES], unspecified |
| D7212 | Drug rash with eosinophilia and systemic symptoms syndrome |
| D7218 | Eosinophilia in diseases classified elsewhere |
| D7219 | Other 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 |
| D75821 | Non-immune heparin-induced thrombocytopenia |
| D75822 | Immune-mediated heparin-induced thrombocytopenia |
| D75828 | Other heparin-induced thrombocytopenia syndrome |
| D75829 | Heparin-induced thrombocytopenia, unspecified |
| D75838 | Other thrombocytosis |
| D75839 | Thrombocytosis, unspecified |
| D7584 | Other platelet-activating anti-PF4 disorders |
| D7589 | Other specified diseases of blood and blood-forming organs |
| D759 | Disease of blood and blood-forming organs, unspecified |
| D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
| 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 |
| 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 |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| 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 |
| D8481 | Immunodeficiency due to conditions classified elsewhere |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D890 | Polyclonal hypergammaglobulinemia |
| 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 |
| D8944 | Hereditary alpha tryptasemia |
| 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 |
| D89831 | Cytokine release syndrome, grade 1 |
| D89832 | Cytokine release syndrome, grade 2 |
| D89833 | Cytokine release syndrome, grade 3 |
| D89834 | Cytokine release syndrome, grade 4 |
| D89835 | Cytokine release syndrome, grade 5 |
| D89839 | Cytokine release syndrome, grade unspecified |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| E320 | Persistent hyperplasia of thymus |
| E321 | Abscess of thymus |
| E328 | Other diseases of thymus |
| E329 | Disease of thymus, unspecified |
| I881 | Chronic lymphadenitis, except mesenteric |
| I888 | Other nonspecific lymphadenitis |
| I889 | Nonspecific lymphadenitis, unspecified |
| I898 | Other specified noninfective disorders of lymphatic vessels and lymph nodes |
| I899 | Noninfective disorder of lymphatic vessels and lymph nodes, unspecified |
| L040 | Acute lymphadenitis of face, head and neck |
| L041 | Acute lymphadenitis of trunk |
| L042 | Acute lymphadenitis of upper limb |
| L043 | Acute lymphadenitis of lower limb |
| L048 | Acute lymphadenitis of other sites |
| L049 | Acute lymphadenitis, unspecified |
| Q8901 | Asplenia (congenital) |
| Q8909 | Congenital malformations of spleen |
| R161 | Splenomegaly, not elsewhere classified |
| R233 | Spontaneous ecchymoses |
| R590 | Localized enlarged lymph nodes |
| R591 | Generalized enlarged lymph nodes |
| R599 | Enlarged lymph nodes, unspecified |
| R710 | Precipitous drop in hematocrit |
| R718 | Other abnormality of red blood cells |
| R75 | Inconclusive laboratory evidence of human immunodeficiency virus [HIV] |
| R760 | Raised antibody titer |
| R768 | Other specified abnormal immunological findings in serum |
| R769 | Abnormal immunological finding in serum, unspecified |
| S3600XA | Unspecified injury of spleen, initial encounter |
| S36020A | Minor contusion of spleen, initial encounter |
| S36021A | Major contusion of spleen, initial encounter |
| S36029A | Unspecified contusion of spleen, initial encounter |
| S36030A | Superficial (capsular) laceration of spleen, initial encounter |
| S36031A | Moderate laceration of spleen, initial encounter |
| S36032A | Major laceration of spleen, initial encounter |
| S36039A | Unspecified laceration of spleen, initial encounter |
| S3609XA | Other injury of spleen, initial encounter |
| T8030XA | ABO incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter |
| T80310A | ABO incompatibility with acute hemolytic transfusion reaction, initial encounter |
| T80311A | ABO incompatibility with delayed hemolytic transfusion reaction, initial encounter |
| T80319A | ABO incompatibility with hemolytic transfusion reaction, unspecified, initial encounter |
| T8039XA | Other ABO incompatibility reaction due to transfusion of blood or blood products, initial encounter |
| T8040XA | Rh incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter |
| T80410A | Rh incompatibility with acute hemolytic transfusion reaction, initial encounter |
| T80411A | Rh incompatibility with delayed hemolytic transfusion reaction, initial encounter |
| T80419A | Rh incompatibility with hemolytic transfusion reaction, unspecified, initial encounter |
| T8049XA | Other Rh incompatibility reaction due to transfusion of blood or blood products, initial encounter |
| T8082XA | Complication of immune effector cellular therapy, initial encounter |
| T8089XA | Other complications following infusion, transfusion and therapeutic injection, initial encounter |
| T80910A | Acute hemolytic transfusion reaction, unspecified incompatibility, initial encounter |
| T80911A | Delayed hemolytic transfusion reaction, unspecified incompatibility, initial encounter |
| T80919A | Hemolytic transfusion reaction, unspecified incompatibility, unspecified as acute or delayed, initial encounter |
| T8092XA | Unspecified transfusion reaction, initial encounter |
| T80A0XA | Non-ABO incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter |
| T80A10A | Non-ABO incompatibility with acute hemolytic transfusion reaction, initial encounter |
| T80A11A | Non-ABO incompatibility with delayed hemolytic transfusion reaction, initial encounter |
| T80A19A | Non-ABO incompatibility with hemolytic transfusion reaction, unspecified, initial encounter |
| T80A9XA | Other non-ABO incompatibility reaction due to transfusion of blood or blood products, initial encounter |
| T8600 | Unspecified complication of bone marrow transplant |
| T8601 | Bone marrow transplant rejection |
| T8602 | Bone marrow transplant failure |
| T8603 | Bone marrow transplant infection |
| T8609 | Other complications of bone marrow transplant |
| Z9481 | Bone marrow transplant status |
| Z9484 | Stem cells transplant status |
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Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 16 Mar 2022 17:08:13 CMS, code-revision=333, description-revision=1331 |