PDX Collection 0557 (continued) |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6182 | Myelophthisis |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D62 | Acute posthemorrhagic anemia |
D640 | Hereditary sideroblastic anemia |
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 |
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 |
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 0558 |
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 0559 |
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 0560 |
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 |
D71 | Functional disorders of polymorphonuclear neutrophils |
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 0561 |
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 |
D71 | Functional disorders of polymorphonuclear neutrophils |
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 0562 |
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 |
D71 | Functional disorders of polymorphonuclear neutrophils |
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 0563 |
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 0564 |
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 0565 |
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 0566 |
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 |