delta-aminolevulinic acid dehydratase porphyria, ADP, plumboporphyria, ALA, porphobilinogen, PBG, coproporphyrin III, erythrocyte protoporphyrin IX, acute hepatic porphyria, ALA dehydratase deficiency porphyria acute lymphoblastic leukemia, ALL, lymphoid precursor cells, lymphoblasts, malignant lymphoid disorder, cancer, bone marrow malignancy, bone marrow cancer, leukemia, bone marrow failure, lymphoma, bone marrow carcinoma, anemia, thrombocytopenia, neutropenia, leukemia in children, bone pain, acute nonlymphoblastic leukemia, acute nonlymphocytic leukemia, acute non-lymphoblastic leukemia, acute non-lymphocytic leukemia, nonlymphoblastic leukemia, nonlymphocytic leukemia, non-lymphoblastic leukemia, non-lymphocytic leukemia, leukemia, cancer, acute myeloid leukemia, AML, bone marrow cancer, bone marrow failure, radiation exposure, Bloom syndrome, Down syndrome, trisomy 21, congenital neutropenia, Fanconi anemia, neurofibromatosis, acute promyelocytic leukemia, APL, M3, promyelocytic leukemia, immature bone marrow cells, chromosomal translocation, genetic abnormality, cytogenetic abnormalities, anemia, thrombocytopenia, neutropenia, myelodysplastic syndrome, MDS, antecedent hematologic disorder, AHD, disseminated intravascular coagulation, DIC, organ infiltration with leukemic cells, leukostasis, familial erythroleukemia, bone marrow transplantation, bone marrow transplant, BMT, allogeneic BMT, autologous BMT, alkylating agents, topoisomerase-II inhibitors, acute monocytic leukemia, M5, acute myelomonocytic leukemia, M4, blast count, acute undifferentiated leukemia, M0, acute megakaryocytic leukemia, M7, bone marrow aspiration, arabinosylcytosine, araC, fibrinolysis, all-trans-retinoic acid, ATRA, retinoic acid syndrome, malignant disease of bone marrow, bleeding gums, multiple ecchymoses, gingivitis, petechiae, leukemia cutis, chloromata, soft-tissue chloroma, granulocytic sarcoma, Li-Fraumeni syndrome, aplastic anemia, pancytopenia, myelofibrosis, paroxysmal nocturnal hemoglobinuria, polycythemia vera AMM, idiopathic myelofibrosis, aleukemic myelosis, myelosclerosis, leukoerythroblastic anemia with diffuse osteosclerosis, megakaryocytic splenomegaly, anemia, bone marrow fibrosis, extramedullary hematopoiesis, leukoerythroblastosis, hepatosplenomegaly, hematopoietic system, chronic myeloid leukemia, chronic myelogenous leukemia, chronic myelocytic leukemia, CML, polycythemia vera, essential thrombocytosis granulocytopenia, neutropenia, neutrophils, absolute neutrophil count, ANC, stomatitis, periodontitis, pharyngitis, autoimmune hemolytic anemia, idiopathic thrombocytopenic neutropenia, Kostmann syndrome, granulocyte colony-stimulating factor, G-CSF, ELA2 α2-plasmin inhibitor deficiency, alpha2-antiplasmin, fast-acting plasmin inhibitor, α2PI deficiency, bleeding disorders, hemostasis, plasmin inhibitors, inherited alpha2-plasmin inhibitor deficiency, acquired alpha2-plasmin inhibitor deficiency, prolonged bleeding, mucosal bleeding, increased bruising, increased hematomas, muscle bleeding, bleeding into joints, excessive bleeding, excessive bruising AL, light chain amyloidosis, primary amyloidosis, primary systemic amyloidosis, myeloma-associated amyloidosis, Ig-related amyloidosis, immunoglobulin-related amyloidosis, monoclonal plasma cell dyscrasias, monoclonal plasma cell disorder, amyloid deposits, amyloid L chain type, multiple myeloma, monoclonal gammopathy of undetermined significance, MGUS, nonamyloid monoclonal immunoglobulin deposition disease, MIDD red blood cell count, RBC, hemoglobin concentration, Hb, hematocrit, Hct, reticulocytes, erythrocytes, sickle cell anemia, thalassemia, malaria, hookworm, chronic infections, iron deficiency, folic acid deficiency, mean corpuscular volume, MCV, mean corpuscular hemoglobin concentration, MCHC, blood loss, increased RBC destruction, hemolysis, decreased production of RBCs, heme iron, anemia, decrease in red blood cell, decrease in RBC mass, hereditary spherocytosis, glucose-6-phosphate dehydrogenase deficiency, G-6-PD deficiency, chronic hemolytic anemia, pernicious anemia, calf cramps, hemoglobinopathies, sex-linked sideroblastic anemias, Fanconi syndrome, use of aspirin, use of nonsteroidal anti-inflammatory drugs, use of NSAIDs, use of Coumadin, gastrointestinal bleeding, tarry stools, neoplasms of colon, hemorrhoidal blood loss, pagophagia, cramps in the calves, sore tongue, cheilosis, steatorrhea, coagulopathy, thrombocytopenia, bleeding disorders, hypothyroidism, lupus erythematosus, paroxysmal cold hemoglobinuria, macroglobulinemias, march hemoglobinuria, paroxysmal nocturnal hemoglobinuria, endocrinopathy, pallor, hepatomegaly, splenomegaly, bacterial endocarditis

enzyme abnormalities of the glycolytic pathways, hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, toxoplasmosis, leishmaniasis, gram-negative sepsis, cytomegalovirus, infectious mononucleosis, hepatitis, collagen vascular diseases, neoplasia, hepatic disease, renal disease, malignancies, chronic diseases, megaloblastic anemia, aplastic anemia, frostbite, burns, trauma, hemorrhage, generalized malnutrition, folate deficiency, vitamin B-12 deficiency, Fanconi anemia, AT deficiency, antithrombin III, AT III, ATIII, anticoagulation, anticoagulant, coagulation factors, hemostatic pathway, coagulation pathway, serine protease inhibitor, deep vein thrombosis, DVT, venous thrombosis, pulmonary embolism, PE, venous thromboembolism, VTE, thrombotic disease, acute respiratory distress syndrome, ARDS, venoocclusive disease, veno-occlusive disease, VOD, bone marrow transplantation, BMT, chronic leg ulcerations, severe venous varicosities, postphlebitic syndrome, low molecular weight heparin, low-molecular-weight heparin, LMWH, pooled plasma treated with solvent-detergent, PLAS+SD, Budd-Chiari syndrome, estrogen, hormone replacement therapy, HRT aplastic anemia, progressive hypocythemia, aregeneratory anemia, aleukia hemorrhagica, panmyelophthisis, hypoplastic anemia, toxic paralytic anemia, bone marrow failure syndrome, peripheral pancytopenia oxygen carriers, artificial oxygen carriers, oxygen-carrying volume expanders, hemoglobin-based oxygen carriers, perfluorocarbons, PFCs, blood, stroma-free hemoglobin bone marrow examination, bone marrow pathology, evaluation of hematologic disorders, bone marrow biopsy, fever of unknown origin, FUO pancytopenia, stem cell defect, hypoplastic anemia, aplastic anemia, single cytopenias, acquired bone marrow failure, inherited bone marrow failure, bone marrow failure syndromes, Fanconi anemia, dyskeratosis congenital, Diamond-Blackfan anemia, inherited bone marrow failure syndromes, IBMFS CLL, monoclonal disorders, well-differentiated lymphoma, small lymphocytic lymphoma, prolymphocytic leukemia, weight loss, extreme fatigue, night sweats, progressive marrow failure, autoimmune anemia, thrombocytopenia, progressive splenomegaly, massive lymphadenopathy, progressive lymphocytosis chronic myelogenous leukemia, CML, chronic granulocytic leukemia, Philadelphia chromosome positive myeloproliferative disorder, lymphoblastic leukemia, leukemia, leukocytosis, splenomegaly, blast crisis, enlarged spleen, lymphoproliferative disorder, blood cell cancer, Philadelphia chromosome, Ph chromosome, BCR/ABL, BCR-ABL severe combined immunodeficiency, SCID, X-linked severe combined immunodeficiency, XSCID, JAK3 deficiency, adenosine deaminase deficiency, ADA deficiency, reticular dysgenesis, X-linked hyper-IgM syndrome, common lymphoid progenitor, CLP, X-linked agammaglobulinemia, XLA, XHM, reticular dysgenesis, cartilage-hair hypoplasia, CHH, malnutrition, HIV infection, combined immunodeficiency, human immunodeficiency virus infection, bacterial pneumonia, viral pneumonia, Pneumocystis carinii infection, P carinii infection, PCP, cytomegalovirus infection, CMV infection, disseminated bacille Calmette-Guerin infection, disseminated BCG infection, atypical mycobacterial infection, skin candidiasis, opportunistic infection, failure to thrive, short-limbed dwarfism, Omenn syndrome, reticular dysgenesis, Wiskott-Aldrich syndrome, WAS, common variable immunodeficiency, CVID Cooley's anemia, beta thalassemia, beta thalassemia major, thalassanemia, splenomegaly, mongoloid facial features, blood disorder, hemoglobin disorder, blood disease, beta thalassemia, beta thalassemia intermedia, beta thalassemia minor, beta thalassemia major, Cooley's anemia, alpha thalassemia, hemoglobin, beta-globin gene production, hemoglobin A DIC, consumptive coagulopathy, bleeding, thrombosis, thrombin, plasmin, disseminated intravascular coagulation congenital dysfibrinogenemia, cirrhosis, hepatoma, hepatitis, abnormal clot formation, fibrinopeptide, fibrinolysis, thrombotic events, fibrin, dysfibrinogenemia of liver disease, acquired dysfibrinogenemia hereditary elliptocytosis, HE, elliptical red cells, Southeast Asian ovalocytosis, SAO, hereditary pyropoikilocytosis, HPP, elliptocytes, hemolytic anemia, folate deficiency, splenectomy eosinophilic leukocytes, idiopathic hypereosinophilic syndrome, HES, CHINA, Ascaris lumbricoides, Löffler syndrome, simple pulmonary eosinophilia, tropical eosinophilia erythroleukemia, Di Guglielmo disease, Di Guglielmo syndrome, acute myelogenous leukemia, AML, neoplastic proliferation, erythroid precursor, myeloid precursor, M6 AML primary erythromelalgia, secondary erythromelalgia, erythermalgia, myeloproliferative disorder, arteriolar fibrosis, idiopathic erythromelalgia, platelet-mediated erythromelalgia, aspirin-sensitive erythromelalgia, primary erythermalgia, secondary erythermalgia, polycythemia vera, essential thrombocytosis acquired factor II deficiency, inherited factor II deficiency, deficiency of factor II, prothrombin deficiency, FII, F II, prothrombin, vitamin K–dependent proenzyme, vitamin K deficiency, prothrombin abnormality, clotting, coagulation, blood coagulation cascade, hypoprothrombinemia, dysprothrombinemia, prothrombin complex concentrates, prothrombin 20210a, thrombophilia hemophilia B, Christmas disease, hemophiliac, hemophilia, blood factors, factor 9, FIX, bleeding disorder, blood disease, blood disorder, hemarthrosis, hematomas, mucocutaneous bleeding, inherited blood disease, familial bleeding disorder, familial blood disease, factor replacement therapy FVII, F7 gene, proconvertin, stable factor, serum prothrombin conversion accelerator, SPCA, autoprothrombin I, recombinant factor VIIa, rFVIIa, NovoSeven, coagulation, procoagulants, coagulation cascade, anticoagulant factors, Dubin-Johnson syndrome, Rotor syndrome, prothrombin conversion accelerator deficiency, coagulation disorder, blood disorder blood disease, hemophilia A, hemophilia, hemophilia B factor VIII coagulant activity, F VIII-C, FVIII-C, F VIII clotting activity, FVIII clotting activity, antihemophilic globulin, blood disease, blood disorder, hematologic disorder, bleeding disorder, hemostatic system, plasma coagulation system, hemophilia A, hemophilia B, hemophilia, haemophilia, hemorrhagic disorder, coagulation disorder, clotting disorder, blood clotting, coagulopathies, coagulopathy factor X deficiency, FX, FX deficiency, Stuart factor, Prower factor, Stuart-Prower factor, autoprothrombin III, thrombokinase, vitamin K deficiency, liver disease, hepatic disease, blood disorder, factor disorder, coagulation disorder, clotting disorder, bleeding disorder, blood factor deficiency, factor deficiency, easy bruising, hematuria, soft tissue hemorrhages, hemarthroses, recurrent epistaxis, menorrhagia, congenital factor X deficiency, acquired factor X deficiency factor XI deficiency, FXI deficiency, hemophilia C, plasma thromboplastin antecedent deficiency, Rosenthal's syndrome, Rosenthal syndrome, PTA deficiency, bleeding disorder plasma transglutaminase, fibrin stabilizing factor, transligase, factor XIII deficiency, fibrin stabilizing factor deficiency, FXIII, FXIII deficiency, rFXIII, FXIIIa, hemophilia, bleeding diathesis, autosomal blood disorder, blood disorder, congenital hemorrhagic diathesis, coagulation disorder, tissue transglutaminase, thrombin folic acid deficiency, folate deficiency, vitamin deficiency, vitamin deficiencies, folate, p-aminobenzoic acid, PABA, polyglutamates, tetrahydrofolic acid, THFA, macrocytosis, hypersegmented polymorphonuclear leucocytes, PMNs, anemia Glanzmann disease, Glanzmann thrombasthenia, Glanzmann's thrombasthenia, hemorrhagic disorders, genetic platelet disorders, platelet glycoprotein IIB, GP IIb, platelet glycoprotein IIIa, GP IIIa, GP IIa/IIIb, defective platelet aggregation, von Willebrand factor, vWF, bleeding G-6-PD deficiency, X-linked disorders, nicotinamide adenine dinucleotide phosphate, NADP+, nicotinamide adenine dinucleotide phosphate, NADPH, enzyme deficiency, chronic nonspherocytic hemolytic anemia, neonatal jaundice, acute hemolytic anemia, fava beans, favism, enzymopathy granulopenia, hypogranulocytosis, neutropenia, neutrophils, eosinophils, basophils, granulocytes, agranulocytosis, granulocytopenia leukemic reticuloendotheliosis, hairy cell leukemia, HCL, chronic lymphoid leukemia, B-cell disease, clonal B-cell lymphocyte, hairy cell leukemia, pancytopenia, anemia, thrombocytopenia, neutropenia, hepatosplenomegaly HCD, gamma-HCD, Franklin disease, rheumatoid arthritis, Sjögren syndrome, lupus erythematosus, autoimmune hemolytic anemia, lymphadenopathy, hepatosplenomegaly, heavy-chain disease, lymphoplasmacytic proliferative disorders mu-HCD, heavy chain disease, HCD, B-cell proliferative disorder, immunoglobulin heavy chain, Ig heavy chain, plasma cell disorder, monoclonal gammopathy of unknown significance, gammopathies, chronic lymphocytic leukemia, CLL, multiple myeloma, plasmacytoma, splenomegaly, peripheral lymphadenopathy, hepatomegaly, osteolytic lesion, pathologic fractures HSCT, bone marrow transplantation, BMT, peripheral blood progenitor cells, PBPCs, peripheral blood progenitor cell transplantation, PBPCT, stem cell transplantation, SCT, hematopoietic stem cell transplantation, HSCT, autologous proximal stem cell rescue, total body irradiation, TBI, allogenic transplant, allogeneic transplant, syngeneic transplant, syngenic transplant, autologous transplant, Hodgkin's disease, Hodgkin's lymphoma, Hodgkin disease, Hodgkin lymphoma, non-Hodgkin lymphoma, NHL, multiple myeloma, breast cancer, germ cell tumors, leukemia, myelodysplastic syndromes, aplastic anemia, thalassemia, sickle cell anemia, neuroblastoma, testicular carcinoma, malignant melanoma, soft tissue sarcoma, small-cell lung cancer, colon cancer, ovarian cancer, uterine cancer, severe combined immunodeficiency disorders, SCID, Wiskott-Aldrich syndrome, WIS, Chediak-Higashi syndrome, graft versus host disease, graft-versus-host disease, graft-vs-host disease, GVHD, National Marrow Donor Program, NMDP HbC disease, mild hemolytic anemia, benign hemoglobinopathies, musculoskeletal pain, joint pain, iron deficiency, iron supplementation, angioid streaks, hemoglobin C, gallstones, pigmented gallstones, malaria, Bruch membrane, retinopathy, cholelithiasis, dental infarction, hemolysis, HbC, splenomegaly Donath-Landsteiner hemolytic anemia, cold-induced immune hemolytic anemia, PCH, paroxysmal cold hemoglobinuria, autoimmune hemolytic anemia, AIHA, intravascular hemolysis, anemia, blood disorder, blood disease, cold exposure, biphasic hemolysin hemolysis, premature erythrocyte destruction, hereditary hemoglobin abnormalities, glucose-6-phosphate dehydrogenase deficiency, G6PD deficiency, G-6-PD deficiency, hereditary spherocytosis, sickle cell anemia, sickle cell trait, sickle cell disease, AIHA, autoimmune hemolytic anemia, microangiopathic anemia, disseminated intravascular coagulation, DIC, hemolytic uremic syndrome, HUS, hemolytic-uremic syndrome, TTP, thrombotic thrombocytopenic purpura, defective prosthetic cardiac valves, parvovirus B19 infection, anemia hemolytic-uremic syndrome, HUS, progressive renal failure, microangiopathic hemolytic anemia, thrombocytopenia, acute renal failure, ARF, thrombotic thrombocytopenic purpura, TTP, thrombotic microangiopathies, TMAs, verotoxin-producing Escherichia coli, E coli, VTEC, hamburger disease, Gasser syndrome, Shiga-like toxin–associated HUS, Stx-HUS, non-Stx–associated HUS, non-Stx-HUS, Shigella dysenteriae, S dysenteriae hemophilia A, HA, hemophilia B, HB, Christmas disease, clotting disorder, blood disease, blood disorder, coagulation disorder, factor VIII, FVIII, factor IX, FIX, factor XIII, FXIII, factor XI, FXI, hemophiliac, thrombin, coagulation cascade, joint hemorrhage, hemophilic arthropathy, acute hemarthroses, hemorrhagic death, F8C gene, F9 gene afibrinogenemia, dysfibrinogenemia, nonplatelet hemostasis, coagulation, thrombosis, thromboses, clotting, thrombophilia, hemorrhage, bleeding, factor V deficiency, FV deficiency, Owren disease, parahemophilia, factor VII deficiency, FVII deficiency, factor VIII deficiency, FVIII deficiency, factor X deficiency, FX deficiency, factor XI deficiency, FXI deficiency, factor XII deficiency, FXII deficiency, factor XIII deficiency, FXIII deficiency, factor V Leiden deficiency, disseminated intravascular coagulation, DIC, protein C deficiency, activated protein C resistance, aPCR, protein S deficiency, hemophilia, antithrombin III deficiency, hemostatic disorders, hypoprothrombinemias, cryoglobulinemias, multiple myeloma, Waldenstrom macroglobulinemia, Henoch-Schönlein purpura, hyperglobulinemic purpura, cavernous hemangioma, hereditary hemorrhagic telangiectasia, pseudoxanthoma elasticum, Ehlers-Danlos syndrome, scurvy, Cushing syndrome,Shwartzman phenomenon, vitamin K deficiency, von Willebrand disease, Waterhouse-Friderichsen syndrome, Wiskott-Aldrich syndrome Hodgkin lymphoma, Hodgkin disease, Hodgkin's disease, Hodgkin's lymphoma, malignant lymphoma, lymph cancer, Epstein-Barr virus, EBV, nodular sclerosis Hodgkin disease, mixed cellularity Hodgkin disease, lymphocyte depleted Hodgkin disease, lymphocyte-depleted Hodgkin disease, lymphocyte-rich Hodgkin disease, nodular Hodgkin disease, nodular lymphocyte-predominant Hodgkin disease, lymph node cancer idiopathic hypereosinophilic syndrome, HES, IHS, IHES, eosinophilia, eosinophilic leukemia, acute eosinophilic leukemia, chronic eosinophilic leukemia, CEL, overproduction of eosinophils immune thrombocytopenic purpura, ITP, autoimmune thrombocytopenia purpura, AITP, idiopathic thrombocytopenic purpura, neonatal alloimmune thrombocytopenia, NAIT, fetomaternal alloimmune thrombocytopenia, FMAIT idiopathic thrombocytopenic purpura, ITP, autoimmune thrombocytopenic purpura, primary thrombocytopenic purpura, thrombocytopenia, purpura, petechiae, thrombocytopenic purpura, bleeding disorder, platelet disorder, splenectomy, intravenous immune globulin therapy, IVIG therapy, IV RhIG therapy, intravenous RhIG therapy, intravenous Rho immune globulin therapy IVIG, gamma globulin, gammaglobulin, intravenous Ig, immunoglobulin preparations, Ig preparations, immunomodulating agents, idiopathic thrombocytopenic purpura, ITP, Kawasaki disease, Kawasaki's disease, graft versus host disease, GVHD, graft vs host disease, graft-vs-host disease, graft-versus-host disease, Guillain-Barre syndrome, polymyositis/dermatomyositis, polymyositis, dermatomyositis, blood disease, hematological disease, hematologic disease, immune dysfunction sideropenia, posthemorrhagic anemia, erythropoiesis, hemosiderosis, sprue, celiac disease, regional enteritis, ferric iron, ferrous iron, small bowel disease, regional enteritis, previous gastrointestinal surgery, intestinal parasites, hookworms, gastrointestinal neoplasms, gastrointestinal bleeding, pica eating, clay eating, starch eating, hematuria, hematemesis, hemoptysis, hemorrhage, melanotic stool, pagophagia, leg cramps, dysphagia with esophageal webbing, koilonychia, glossitis, angular stomatitis, gastric atrophy, atrophic changes of the tongue, splenomegaly, phytates, oxalates, phosphates, carbonates, tannates, hemosiderinuria, hemoglobinuria, pulmonary hemosiderosis, paroxysmal nocturnal hemoglobinuria, brisk intravascular hemolytic anemia, prolonged achlorhydria, celiac syndrome, sex-linked anemia, microcytic anemia, metabolic processes KMS, Kaposi hemangioendothelioma, Kaposi's hemangioendothelioma, kaposiform hemangioendothelioma, consumptive thrombocytopenia, thrombocytopenic purpura, tufted angiomas, vascular lesions, ecchymotic lesions, interferon alfa, Kasabach Merritt syndrome, vascular tumor, mitogen KD, histiocytic necrotizing lymphadenitis, cervical lymphadenopathy, Kikuchi disease, Kikuchi-Fujimoto disease, Kikuchi's disease, lymph node enlargement, lymphoma, systemic lupus erythematosus, SLE, upper respiratory tract infections, URTIs, cytomegalovirus, Epstein-Barr virus, human herpesvirus, varicella-zoster virus, parainfluenza virus, parvovirus B19, paramyxovirus, lymphadenitis LCDD, light chain disease, renal disease, renal insufficiency, proteinuria, nephrotic syndrome, multiple myeloma, lymphoproliferative disease, end-stage renal disease, ESRD, light-chain deposition disease non-Hodgkin lymphoma, NHL, lymph node, lymphoid tissue, indolent lymphomas, aggressive lymphomas, Burkitt lymphoma, B-cell neoplasms, T/NK-cell neoplasms, Hodgkin lymphoma, Hodgkin's lymphoma, B-cell chronic lymphocytic leukemia, CLL, B-cell CLL, B-cell small lymphocytic lymphoma, lymphoblastic lymphomas, T-cell acute lymphocytic leukemias, diffuse large B-cell lymphoma, follicular lymphoma, follicular large cell lymphoma, mantle cell NHL, small lymphocytic lymphoma, splenic marginal zone lymphoma, extranodal B-cell lymphoma of mucosa-associated lymphoid tissue, MALT, mediastinal diffuse large B-cell lymphoma, indolent NHL, lymphoproliferative malignancy, lymphoproliferative disease, Revised European-American Lymphoma Classification, REAL Classification, immunocytoma, mycosis fungoides, Sézary syndrome, lymphadenopathy, Waldeyer ring, bcl-2 apoptotic inhibitor oncogene cutaneous T-cell lymphoma, CTCL, lymphoma, skin cancer, lymphoproliferative disorder, mycosis fungoides, MF, Sézary syndrome, follicular MF, pagetoid reticulosis, Woringer-Kolopp disease, anaplastic large cell lymphoma, ALCL, lymphomatoid papulosis, LyP, peripheral T-cell lymphoma, PTCL diffuse large cell lymphoma, intermediate-grade lymphoma, large cell lymphoma, immunoblastic lymphoma, non-Hodgkin lymphoma, NHL intermediate grade lymphoma, diffuse small and large cell lymphoma, malignant lymphoma, diffuse mixed type, intermediate-grade lymphoma, mixed histiocytic-lymphocytic malignant lymphoma, malignant lymphoma, mixed small and large cell lymphoma, diffuse mixed lymphomas, cancer, malignant histiocytes, malignant lymphocytes follicular lymphoma, nodular lymphomas, low-grade lymphomas, indolent lymphomas, non-Hodgkin Lymphoma, lymphoid tissue, lymph nodes, spleen, bone marrow, primary extranodal lymphoma high-grade lymphoma, large-cell immunoblastic lymphoma, high-grade malignant immunoblastic lymphoma, diffuse histiocytic lymphoma, diffuse large B-cell lymphoma, DLBCL, immunoblastic lymphoma, IBL, B-cell disorder, high-grade non-Hodgkin lymphoma, NHL, high-grade NHL, intermediate-grade NHL, diffuse large cell NHL, diffuse large-cell NHL, diffuse large cell lymphoma, diffuse large-cell lymphoma, DLCL, cancer lymphoblastic lymphoma, LBL, non-Hodgkin lymphoma, NHL, non-Hodgkin's lymphoma, acute lymphoblastic leukemia, ALL, cancer, childhood cancer, painless lymphadenopathy, constitution B symptoms, neoplastic disease, cancerous tumor, lymph node biopsy, LNB, high-grade lymphoma, immunoblastic lymphoma, malignant lymphoproliferative disorder, lymph node–based disease anaplastic large cell lymphoma, ALCL, anaplastic lymphoma kinase-positive lymphoma, ALK-positive lymphoma, anaplastic Ki-1+ large cell lymphoma, lymphoma, large cell anaplastic CD30+ Ki-1 lymphoma, Ki-1 large cell lymphoma, cutaneous and nodal Ki-1 positive anaplastic large cell lymphoma, cutaneous lymphoma, skin cancer, cancer, extranodal lymphoma, extra-nodal lymphoma, systemic lymphoma, systemic cancer, anaplastic lymphoma small noncleaved cell lymphoma, SNCC lymphoma, Burkitt's lymphoma in children, Burkitt lymphoma in children, BL, Burkittlike lymphoma in adults, BLL, high-grade non-Hodgkin lymphoma, high-grade non-Hodgkin's lymphoma, NHL, B-cell lymphoma MCL, lymphocytic lymphoma of intermediate differentiation, intermediate lymphocytic lymphoma, ILL, diffuse poorly differentiated lymphocytic lymphoma, PDL, centrocytic lymphoma, diffuse small-cleaved cell lymphoma, DSCCL, mental zone lymphoma primary mediastinal B-cell lymphoma, PMBL, B-cell neoplasm non-Hodgkin lymphoma, NHL, non-Hodgkin's lymphoma, Hodgkin disease, Hodgkin's disease, Revised European-American Lymphoma classification, REAL classification, lymphoid tissues, lymph, hematopoietic neoplasm, mantle cell lymphoma, T/NK lymphoma, Burkitt lymphoma, Burkitt's lymphoma, indolent NHL, follicular lymphoma, small lymphocytic lymphoma, SLL, lymphoplasmacytoid lymphoma, marginal zone lymphoma, diffuse large B-cell lymphoma, immunoblastic lymphoma, anaplastic lymphoma, lymphoblastic lymphoma, Burkitt-like lymphoma, Burkitt's-like lymphoma XLP syndrome, Duncan syndrome, Duncan's syndrome, X-linked recessive progressive combined variable immunodeficiency syndrome, Epstein-Barr virus, EBV, infectious mononucleosis, hypogammaglobulinemia, lymphoma, lymphoproliferative diseases megaloblastic anemia, vitamin B-12 deficiency, folate deficiency, chronic alcoholism, accelerated erythropoiesis, alcoholism, chronic obstructive pulmonary disease, COPD, Lesch-Nyhan syndrome, deficient enzymes for folate metabolism, homocystinuria, myelodysplastic anemia, myelophthisic anemia, aplastic anemia, acquired sideroblastic anemia, liver disease, hypothyroidism systemic mast cell disease, SMCD, cutaneous mastocytosis, urticaria pigmentosa, systemic mastocytosis, mast cell disease, extracutaneous mast cell disease, extra-cutaneous mast cell disease, myeloproliferative disease, myeloproliferative disorders blood disorder, megaloblastosis, cobalamin deficiency, vitamin B-12 deficiency, folate deficiency, pernicious anemia, PA, cobalamin neuropathy, ineffective erythropoiesis, food-cobalamin malabsorption, gastrectomy, Zollinger-Ellison syndrome, ZES, ileal resection, regional ileitis, intestinal lymphoma, Diphyllobothrium latum, D latum, fish tapeworm, blind loop syndrome, nitrous oxide exposure, NO exposure, surgical intestinal resection, amyloidosis, Whipple disease, scleroderma, psoriasis, exfoliative dermatitis, pregnancy, neural tube defects, drug reactions, chemotherapy, neurological impairment methemoglobin, metHB, NADH-metHb reductase deficiencies, acquired methemoglobinemia, enterogenous methemoglobinemia, secondary methemoglobinemia, congenital methemoglobinemia, hereditary methemoglobinemia, hereditary methemoglobinemic cyanosis, primary methemoglobinemia, cyanosis, cytochrome b5reductase deficiency, hemoglobin M monoclonal gammopathy of undetermined significance, MGUS, plasma cell dyscrasias, multiple myeloma, MM, Waldenström macroglobulinemia, WM, AL amyloidosis, other lymphoproliferative disorders lymphoid tissue, lymph node, mucus membrane, mucus, mucosal tissue, tonsils, Peyer patches, Peyer's patches, vermiform appendix, non-Hodgkin lymphoma, non-Hodgkin's lymphoma, NHL, lymphoma, malignancy, malignancies, cancer, Hashimoto thyroiditis, Hashimoto's thyroiditis, Crohn disease, Crohn's disease, celiac disease, Sjögren syndrome, Helicobacter pylori, H pylori, MALT, gut-associated lymphoid tissue, GALT, bronchial/tracheal-associated lymphoid tissue, BALT, nose-associated lymphoid tissue, NALT, vulvovaginal-associated lymphoid tissue, VALT, MALToma, MALT lymphoma, gastric MALT lymphoma, nongastric MALT lymphoma, gastric MALToma, nongastric MALToma, human mucosa myeloma, bone marrow malignancy, bone marrow cancer, myeloma multiple, plasma cell myeloma, Kahler's disease, Kahler disease, plasma cell dyscrasia, plasma cell leukemia, leukopenia, anemia, thrombocytopenia, bone pain, hypercalcemia, spinal cord compression, hyperviscosity, amyloidosis, renal failure, monoclonal gammopathy of unknown significance, MGUS, M and P chemotherapy, leukemia, plasma cell leukemia, VAD chemotherapy, plasmacytoma, renal impairment, compression fracture of vertebral body, shingles, herpes zoster, Haemophilus infections, epistaxis, stroke, myocardial ischemia, myocardial infarction, carpal tunnel syndrome, meningitis, peripheral neuropathies, ecchymoses, purpura, macroglossia mycosis fungoides, MF, cutaneous T-cell lymphoma, CTCL, Sézary syndrome, SS, erythroderma, malignant lymphoma, skin lesions, Staphylococcus aureus, S aureus, Pseudomonas aeruginosa, P aeruginosa MDS, preleukemia, refractory dysmyelopoietic anemia, smoldering leukemia, subacute myelogenous leukemia, dysmyelopoiesis, refractory anemia, RA, RA with ringed sideroblasts, RARS, RA with excess blasts, RAEB, RAEB in transformation, RAEB-T, anemia, blood disease, hematopoietic disorders, leukemia, acute leukemia, refractory anemia with ringed sideroblasts, refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, chronic myelomonocytic leukemia, CMML, hematopoietic stem cell injury, apoptosis, programmed cell death, petechiae, thrombocytopenia, neutropenia, epistaxis, gum bleeding, hemoptysis, hematuria, enlarged spleen, pneumonias, urinary tract infections, secondary acute leukemia, primary MDS, secondary MDS, leukemogenic chemicals, insecticides, weed killers, fungicides myelophthisis, secondary myelofibrosis, marrow infiltration, marrow granuloma, infiltrative myelopathy, nonhematopoietic cells, cytopenia, thrombocytopenia, neutropenia, pancytopenia MPD, polycythemia vera, PV, polycythemia rubra vera, primary thrombocythemia, PT, agnogenic myeloid metaplasia, AMM, chronic myelogenous leukemia, CML, myelofibrosis, MF, acute leukemia, myelodysplastic syndrome, essential thrombocythemia, ET, Budd-Chiari syndrome, chronic idiopathic myelofibrosis, CIM, chronic neutrophilic leukemia, (CNL), chronic eosinophilic leukemia (CEL), hypereosinophilic syndrome, HES neutropenia, Schultz disease, agranulocytosis, granulocytopenia, leukopenia, neutropenic fever, circulating neutrophils, granulocyte colony-stimulating factor, G-CSF, bone marrow transplantation leukocytosis, granulocytosis, neutrophils, host defense PNH, hemolytic anemia, hemoglobinuria, hemosiderinuria, Marchiafava-Micheli syndrome, dark-colored urine, hemolysis, paroxysmal nocturnal hemoglobinuria vitamin B-12 deficiency, cobalamin deficiency, Cbl deficiency, addisonian anemia, Biermer anemia, Hunter-Addison anemia, Lederer anemia, Biermer-Ehrlich anemia, Addison-Biermer disease, macrocytic achylic anemia, malignant anemia, cobalamine deficiency, adenosylcobalamin, methylcobalamin, intrinsic factor, IF, macrocytic anemia, neurological complications, severe gastric atrophy, achlorhydria, gastrectomy, gastric stapling, bypass procedures for obesity, extensive infiltrative disease of the gastric mucosa, Zollinger-Ellison syndrome, tropical sprue, regional enteritis, ulcerative colitis, ileal lymphoma, Imerslьnd-Grasbeck syndrome, chronic pancreatitis, sore tongue, smooth tongue with loss of papillae, paresthesias, megaloblastic madness, tapeworm infestation, Diphyllobothrium latum, congenital pernicious anemia, hereditary transcobalamin I deficiency, megaloblastic anemia, homocystinuria, homocystinemia plasma cell tumor, plasmocytoma, plasmacytoma of the skeletal system, solitary bone plasmacytoma, SBP, soft tissue plasmacytoma, SEP, extramedullary plasmacytoma, neoplastic monoclonal cell, bone marrow platelet disorders, autoimmune thrombocytopenia, alloimmune thrombocytopenia, drug-induced thrombocytopenia, thrombotic thrombocytopenic purpura, blood disorders, bleeding disorders, hematologic disorders, hemostatic disorders, clotting disorders, hemostatic plug, prolonged bleeding time, petechiae, purpura, immune thrombocytopenic purpura, ITP, TTP, posttransfusion purpura, post-transfusion purpura, neonatal alloimmune thrombocytopenia, hemolytic uremic syndrome, HUS, von Willebrand disease, vWD, Bernard-Soulier syndrome, Glanzmann thrombasthenia, diffuse intravascular coagulation, DIC polycythemia vera, PV, plethora vera, primary polycythemia, stem cell disorders, bone marrow disorder, red cell hyperproliferation, increased red blood cells, blood hyperviscosity, impaired microcirculation, leukemia, red blood cell hyperproliferation, bone marrow cancer, bone marrow neoplasm, marrow neoplasm, bone marrow malignancy, neoplastic marrow disorder, panhyperplastic marrow disorder, pan-hyperplastic marrow disorder, malignant marrow disorder, unregulated neoplastic proliferation, Budd-Chiari syndrome, hepatic portal vein thrombosis, mesenteric vein thrombosis, uncontrolled red blood cell production, panmyelosis, myeloproliferative disease, MPD, hyperhomocystinemia, acquired von Willebrand syndrome, von Willebrand factor, headache, dizziness, vertigo, tinnitus, angina pectoris, intermittent claudications, epistaxis, gum bleeding, ecchymoses, GI bleeding, venous thrombosis, thromboembolism, stroke, arterial thromboses, splenomegaly, splenic infarction, hepatomegaly, plethora, ruddy complexion, hypertension, deletion of 20q, deletion of 13q, trisomy 8 , trisomy 9, trisomy of 1q, deletion of 5q, monosomy 5, deletion of 7q, monosomy 7, Janus kinase-2, JAK2 polycythemia, secondary erythrocytosis, hypoxemia-induced polycythemia, myeloproliferative disorders, secondary polycythemia, secondary polycythemic disorders, congenital heart disease, hypoxia, tissue hypoxia, blood disorder, secondary blood disorder, erythrocythemia acute intermittent porphyria, AIP, defects in heme metabolism, increased secretion of porphobilinogen, abdominal pain, psychiatric problems, hysteria, peripheral neuropathies, abdominal pain, neuropathy, constipation Dobson's complaint, heme biosynthesis, enzyme defects, acute intermittent porphyria, AIP, acute porphyria, intermittent acute porphyria, IAP, biochemical defects, variegate porphyria, VP, neurovisceral dysfunction, metabolism error, hypertension, abdominal colic, psychosis, neuropathy, Chester porphyria gene, inborn error of metabolism, porphobilinogen deaminase, protoporphyrinogen oxidase coproporphyria, defects in heme metabolism, excessive secretion of porphyrins, excessive secretion of porphyrin precursors, abdominal pain, peripheral neuropathies, psychiatric disturbance, hysteria protein C deficiency, thrombophilia, hypercoagulability, anticoagulant protein C, thrombosis, deep venous thrombosis, acquired protein C deficiency, zymogen, protein S, factor X, prothrombin, arterial thrombosis, activated protein C, APC purpura fulminans, protein S deficiency, vitamin K–dependent anticoagulant protein, protein S, activated protein C, APC, activated factor V, FVa, activated factor VIII, FVIIIa, thrombosis, venous thromboembolism, VTE, arterial thrombosis X-linked immunodeficiency with hyper-IgM, XHM, common variable immunodeficiency, CVID, immunodeficiency, immunodeficiencies, lymphoma, leukemia, B-cell immunodeficiency, B-cell immunodeficiencies, primary lymphopoiesis, PL, secondary lymphopoiesis, SL, X-linked agammaglobulinemia, XLA, Bruton agammaglobulinemia, IgA deficiency, immunoglobulin A deficiency, selective immunoglobulin M deficiency, selective IgM deficiency, Wiskott-Aldrich syndrome, WAS, malnutrition, antibody deficiency syndrome, B-cell disorder, B cell disorder, hypogammaglobulinemia, Good syndrome, transient hypogammaglobulinemia of infancy, THI, immunodeficiency with thymoma, IgG subclass deficiency, immunoglobulin G subclass deficiency, IgE hypogammaglobulinemia, immunoglobulin E hypogammaglobulinemia, Omenn syndrome, Job syndrome, hyperimmunoglobulin E syndrome, HIE syndrome, kappa light-chain deficiency, lambda light-chain deficiency PRCA, red blood cell aplasia, pure red blood cell aplasia, red cell aplasia, erythroblastic hypoplasia, erythroblastopenia, erythroid hypoplasia, red cell agenesis, absence of red blood cell precursors in bone marrow, RBC precursors, erythroid precursors, absence of reticulocytes, normoblastic normochromic anemia, normoblastic-normochromic anemia, Diamond-Blackfan syndrome, anemia, aplasia hereditary pyropoikilocytosis, congenital hemolytic anemia, homozygous hereditary elliptocytosis, partial spectrin deficiency, growth retardation, frontal bossing, gallbladder disease, irregular red blood cells, severe anemia, abnormal red blood cell morphology, splenectomy, low hemoglobin level, nonhemolytic hereditary elliptocytosis, spectrin deficiency, autosomal recessive gene hemoglobin SS disease, homozygous hemoglobin S disease, sickle cell disease, SCD, mutant hemoglobins, Hb S, Hb SS, Hb A, Hb SA, anemia, red blood cells, RBC, sickle shaped, vasoocclusive crisis, sickle cell crisis hereditary spherocytosis, HS, familial hemolytic disorder, hemolytic anemia, anemia, blood disorder, hereditary hemolytic anemia, aplastic crisis, megaloblastic crisis, hemolytic crisis, cholecystitis, cholelithiasis, neonatal hemolysis, splenomegaly enlarged spleen, splenic enlargement, subacute bacterial endocarditis, SBE, infectious mononucleosis, hereditary spherocytosis, thalassemia major, splenic vein thrombosis, portal hypertension, chronic myeloid metaplasia, sarcoidosis, neoplasm, chronic lymphocytic leukemia, CLL, lymphoma, trauma, cyst, hemangioma, metastasis, giant abscess, tropical splenomegaly syndrome, hyperactive malarial syndrome, splenic injury, splenectomy, hypersplenism acanthocyte cell hemolytic anemia, acanthocytosis, neuroacanthocytosis, abetalipoproteinemia, chorea-acanthocytosis syndrome, McLeod phenotype hemoglobin H, hydrops fetalis, alpha thalassemia minor, alpha thalassemia major, thalassemia intermedia, alpha globin chains, beta globin chains, silent carrier state, homozygous alpha+ thalassemia, heterozygous alpha0 thalassemia, hemoglobin H disease, hemoglobin Barts, hydrops fetalis beta thalassemia syndromes, Cooley anemia, Mediterranean anemia, thalassemia major, thalassemia intermedia, thalassemia minor, thalassemia trait, hemoglobin E, hereditary disorder essential thrombocytosis, ET, primary thrombocythemia, idiopathic thrombocythemia, essential thrombocythemia, vascular thrombosis, acute myelogenous leukemia, AML, chronic myelogenous leukemia, CML reactive thrombocytosis, thrombocythemia, bone marrow progenitor cells, pro-inflammatory cytokines, granulocyte colony-stimulating factor, G-CSF, granulocyte-macrophage colony-stimulating factor, GM-CSF, clonal thrombocytosis, platelet, secondary thrombocytosis, benign, interleukin, IL, IL-1, IL-6, IL-11 Moschowitz syndrome, thrombotic thrombocytopenic purpura, TTP, hemolytic-uremic syndrome, HUS, microangiopathic hemolytic anemia, von Willebrand factor, vWF, bland thrombi, petechiae, paralysis, coma blood transfusions, blood products, acute hemolytic transfusion reactions, transfusion complications, blood product reactions, allergic transfusion reaction, blood type, circulatory volume overload, anaphylactic transfusion reaction, blood anaphylaxis, hemolytic reactions, allergic reactions, anaphylactic reaction, anaphylaxis, transfusion-related acute lung injury, TRALI, transfusion-related lung injury, ABO antibody reaction, blood contamination, contaminated blood Waldenström hypergammaglobulinemia, malignant lymphoproliferative disease, monoclonal gammopathy, malignant monoclonal gammopathies, Waldenström macroglobulinemia, Waldenstrom macroglobulinemia, WM, lymphoproliferative disorder, clonal disorder, B-lymphocyte disorder, blood malignancy, hematologic malignancy, blood cell cancer von Willebrand disease, von Willebrand's disease, vWD, VWD, von Willebrand factor, VWF, vWF, mucocutaneous bleeding disorder, primary hemostasis impairment, bleeding disorder, hematological disorder, partial quantitative deficiency, qualitative deficiency, total deficiency