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 |
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 |
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 |
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 |
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 |
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 |
D848 | Other specified immunodeficiencies |
D849 | Immunodeficiency, unspecified |
D890 | Polyclonal hypergammaglobulinemia |
D892 | Hypergammaglobulinemia, unspecified |
D893 | Immune reconstitution syndrome |
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 |
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 |
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 |