| PDX Collection 0509 (continued) |
| 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 |
| 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 |
| D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
| D57214 | Sickle-cell/Hb-C disease with dactylitis |
| D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
| D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
| D573 | Sickle-cell trait |
| D5740 | Sickle-cell thalassemia without crisis |
| D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
| D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
| D57419 | Sickle-cell thalassemia, unspecified, with crisis |
| 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 |
| D5910 | Autoimmune hemolytic anemia, unspecified |
| D5911 | Warm autoimmune hemolytic anemia |
| D5912 | Cold autoimmune hemolytic anemia |
| D5913 | Mixed type autoimmune hemolytic anemia |
| D5919 | Other autoimmune hemolytic anemia |
| D592 | Drug-induced nonautoimmune hemolytic anemia |
| D5930 | Hemolytic-uremic syndrome, unspecified |
| D5931 | Infection-associated hemolytic-uremic syndrome |
| D5932 | Hereditary hemolytic-uremic syndrome |
| D5939 | Other hemolytic-uremic syndrome |
| D594 | Other nonautoimmune hemolytic anemias |
| D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
| D596 | Hemoglobinuria due to hemolysis from other external causes |
| D598 | Other acquired hemolytic anemias |
| D599 | Acquired hemolytic anemia, unspecified |
| D600 | Chronic acquired pure red cell aplasia |
| D601 | Transient acquired pure red cell aplasia |
| D608 | Other acquired pure red cell aplasias |
| D609 | Acquired pure red cell aplasia, unspecified |
| D6101 | Constitutional (pure) red blood cell aplasia |
| D6102 | Shwachman-Diamond syndrome |
| D6103 | Fanconi anemia |
| 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 |
| 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 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 |
| D6911 | Glanzmann thrombasthenia |
| D6919 | Other 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 |
| D6911 | Glanzmann thrombasthenia |
| D6919 | Other 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 |
| D6911 | Glanzmann thrombasthenia |
| D6919 | Other 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 |
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