| PDX Collection 0509 (continued) |
| D6851 | Activated protein C resistance |
| D6852 | Prothrombin gene mutation |
| D6859 | Other primary thrombophilia |
| D6861 | Antiphospholipid syndrome |
| D6862 | Lupus anticoagulant syndrome |
| D6869 | Other thrombophilia |
| 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| T792XXA | Traumatic secondary and recurrent hemorrhage and seroma, initial encounter |
| |
| PDX Collection 0510 |
| D474 | Osteomyelofibrosis |
| 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 |
| D75821 | Non-immune heparin-induced thrombocytopenia |
| D75822 | Immune-mediated heparin-induced thrombocytopenia |
| D75828 | Other heparin-induced thrombocytopenia syndrome |
| D75829 | Heparin-induced thrombocytopenia, 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| |
| PDX Collection 0511 |
| D474 | Osteomyelofibrosis |
| 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 |
| D75821 | Non-immune heparin-induced thrombocytopenia |
| D75822 | Immune-mediated heparin-induced thrombocytopenia |
| D75828 | Other heparin-induced thrombocytopenia syndrome |
| D75829 | Heparin-induced thrombocytopenia, unspecified |
| 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| |
| PDX Collection 0512 |
| D474 | Osteomyelofibrosis |
| 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 |
| D68311 | Acquired hemophilia |
| D68312 | Antiphospholipid antibody with hemorrhagic disorder |
| D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
| D6851 | Activated protein C resistance |
| D6852 | Prothrombin gene mutation |
| D6859 | Other primary thrombophilia |
| D6861 | Antiphospholipid syndrome |
| D6862 | Lupus anticoagulant syndrome |
| D6869 | Other thrombophilia |
| 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 |
| D711 | Leukocyte adhesion deficiency |
| D718 | Other functional disorders of polymorphonuclear neutrophils |
| D719 | Functional disorders of polymorphonuclear neutrophils, unspecified |
| D720 | Genetic anomalies of leukocytes |
| 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 |
| D7381 | Neutropenic splenomegaly |
| 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| |
| PDX Collection 0513 |
| D474 | Osteomyelofibrosis |
| D68312 | Antiphospholipid antibody with hemorrhagic disorder |
| D6851 | Activated protein C resistance |
| D6852 | Prothrombin gene mutation |
| D6859 | Other primary thrombophilia |
| D6861 | Antiphospholipid syndrome |
| D6862 | Lupus anticoagulant syndrome |
| D6869 | Other thrombophilia |
| 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 |
| D711 | Leukocyte adhesion deficiency |
| D718 | Other functional disorders of polymorphonuclear neutrophils |
| D719 | Functional disorders of polymorphonuclear neutrophils, unspecified |
| D720 | Genetic anomalies of leukocytes |
| 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 |
| D7381 | Neutropenic splenomegaly |
| 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| |
| PDX Collection 0514 |
| D474 | Osteomyelofibrosis |
| D68312 | Antiphospholipid antibody with hemorrhagic disorder |
| D6851 | Activated protein C resistance |
| D6852 | Prothrombin gene mutation |
| D6859 | Other primary thrombophilia |
| D6861 | Antiphospholipid syndrome |
| D6862 | Lupus anticoagulant syndrome |
| D6869 | Other thrombophilia |
| 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 |
| D711 | Leukocyte adhesion deficiency |
| D718 | Other functional disorders of polymorphonuclear neutrophils |
| D719 | Functional disorders of polymorphonuclear neutrophils, unspecified |
| D720 | Genetic anomalies of leukocytes |
| 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 |
| D7381 | Neutropenic splenomegaly |
| D75838 | Other thrombocytosis |
| D75839 | Thrombocytosis, unspecified |
| 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| |
| PDX Collection 0515 |
| D474 | Osteomyelofibrosis |
| 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 |
| 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 |
| D892 | Hypergammaglobulinemia, unspecified |
| |
| PDX Collection 0516 |
| D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
| 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 |
| 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 |
| D644 | Congenital dyserythropoietic anemia |
| D6481 | Anemia due to antineoplastic chemotherapy |
| D6489 | Other specified anemias |
| D649 | Anemia, unspecified |
| D740 | Congenital methemoglobinemia |
| D748 | Other methemoglobinemias |
| D749 | Methemoglobinemia, unspecified |
| D759 | Disease of blood and blood-forming organs, unspecified |
| |
| PDX Collection 0517 |
| 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 |
| 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 |
| D65 | Disseminated intravascular coagulation [defibrination syndrome] |
| 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 |
| D72818 | Other decreased white blood cell count |
| D72819 | Decreased white blood cell count, unspecified |
| D75821 | Non-immune heparin-induced thrombocytopenia |
| D75822 | Immune-mediated heparin-induced thrombocytopenia |
| D75828 | Other heparin-induced thrombocytopenia syndrome |
| D75829 | Heparin-induced thrombocytopenia, unspecified |
| D7584 | Other platelet-activating anti-PF4 disorders |
| D759 | Disease of blood and blood-forming organs, unspecified |
| D761 | Hemophagocytic lymphohistiocytosis |
| |
| PDX Collection 0518 |
| 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 |
| 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 |
| D65 | Disseminated intravascular coagulation [defibrination syndrome] |
| 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 |
| D72818 | Other decreased white blood cell count |
| D72819 | Decreased white blood cell count, unspecified |
| D75821 | Non-immune heparin-induced thrombocytopenia |
| D75822 | Immune-mediated heparin-induced thrombocytopenia |
| D75828 | Other heparin-induced thrombocytopenia syndrome |
| D75829 | Heparin-induced thrombocytopenia, unspecified |
| D7584 | Other platelet-activating anti-PF4 disorders |
| D759 | Disease of blood and blood-forming organs, unspecified |
| D762 | Hemophagocytic syndrome, infection-associated |
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