PDX Collection 0501 (continued) |
D569 | Thalassemia, unspecified |
D5700 | Hb-SS disease with crisis, unspecified |
D5701 | Hb-SS disease with acute chest syndrome |
D5702 | Hb-SS disease with splenic sequestration |
D571 | Sickle-cell disease without crisis |
D5720 | Sickle-cell/Hb-C disease without crisis |
D57211 | Sickle-cell/Hb-C disease with acute chest syndrome |
D57212 | Sickle-cell/Hb-C disease with splenic sequestration |
D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
D573 | Sickle-cell trait |
D5740 | Sickle-cell thalassemia without crisis |
D57411 | Sickle-cell thalassemia with acute chest syndrome |
D57412 | Sickle-cell thalassemia with splenic sequestration |
D57419 | Sickle-cell thalassemia with crisis, unspecified |
D5780 | Other sickle-cell disorders without crisis |
D57811 | Other sickle-cell disorders with acute chest syndrome |
D57812 | Other sickle-cell disorders with splenic sequestration |
D57819 | Other sickle-cell disorders with crisis, unspecified |
D580 | Hereditary spherocytosis |
D581 | Hereditary elliptocytosis |
D582 | Other hemoglobinopathies |
D588 | Other specified hereditary hemolytic anemias |
D589 | Hereditary hemolytic anemia, unspecified |
D590 | Drug-induced autoimmune hemolytic anemia |
D591 | Other autoimmune hemolytic anemias |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D593 | Hemolytic-uremic syndrome |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6182 | Myelophthisis |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D62 | Acute posthemorrhagic anemia |
D630 | Anemia in neoplastic disease |
D631 | Anemia in chronic kidney disease |
D638 | Anemia in other chronic diseases classified elsewhere |
D640 | Hereditary sideroblastic anemia |
D641 | Secondary sideroblastic anemia due to disease |
D642 | Secondary sideroblastic anemia due to drugs and toxins |
D643 | Other sideroblastic anemias |
D644 | Congenital dyserythropoietic anemia |
D6481 | Anemia due to antineoplastic chemotherapy |
D6489 | Other specified anemias |
D649 | Anemia, unspecified |
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 |
D7581 | Myelofibrosis |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
T792XXA | Traumatic secondary and recurrent hemorrhage and seroma, initial encounter |
|
PDX Collection 0502 |
D474 | Osteomyelofibrosis |
D65 | Disseminated intravascular coagulation [defibrination syndrome] |
D66 | Hereditary factor VIII deficiency |
D67 | Hereditary factor IX deficiency |
D680 | Von Willebrand's disease |
D681 | Hereditary factor XI deficiency |
D682 | Hereditary deficiency of other clotting factors |
D68311 | Acquired hemophilia |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
D6832 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
D684 | Acquired coagulation factor deficiency |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D688 | Other specified coagulation defects |
D689 | Coagulation defect, unspecified |
D690 | Allergic purpura |
D691 | Qualitative platelet defects |
D692 | Other nonthrombocytopenic purpura |
D693 | Immune thrombocytopenic purpura |
D6941 | Evans syndrome |
D6942 | Congenital and hereditary thrombocytopenia purpura |
D6949 | Other primary thrombocytopenia |
D6951 | Posttransfusion purpura |
D6959 | Other secondary thrombocytopenia |
D696 | Thrombocytopenia, unspecified |
D698 | Other specified hemorrhagic conditions |
D699 | Hemorrhagic condition, unspecified |
D7581 | Myelofibrosis |
D7582 | Heparin induced thrombocytopenia (HIT) |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 0503 |
D474 | Osteomyelofibrosis |
D65 | Disseminated intravascular coagulation [defibrination syndrome] |
D66 | Hereditary factor VIII deficiency |
D67 | Hereditary factor IX deficiency |
D680 | Von Willebrand's disease |
D681 | Hereditary factor XI deficiency |
D682 | Hereditary deficiency of other clotting factors |
D68311 | Acquired hemophilia |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
D6832 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
D684 | Acquired coagulation factor deficiency |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D688 | Other specified coagulation defects |
D689 | Coagulation defect, unspecified |
D690 | Allergic purpura |
D691 | Qualitative platelet defects |
D692 | Other nonthrombocytopenic purpura |
D693 | Immune thrombocytopenic purpura |
D6941 | Evans syndrome |
D6942 | Congenital and hereditary thrombocytopenia purpura |
D6949 | Other primary thrombocytopenia |
D6951 | Posttransfusion purpura |
D6959 | Other secondary thrombocytopenia |
D696 | Thrombocytopenia, unspecified |
D698 | Other specified hemorrhagic conditions |
D699 | Hemorrhagic condition, unspecified |
D7582 | Heparin induced thrombocytopenia (HIT) |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 0504 |
D474 | Osteomyelofibrosis |
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 |
D721 | Eosinophilia |
D72810 | Lymphocytopenia |
D72818 | Other decreased white blood cell count |
D72819 | Decreased white blood cell count, unspecified |
D72820 | Lymphocytosis (symptomatic) |
D72821 | Monocytosis (symptomatic) |
D72822 | Plasmacytosis |
D72823 | Leukemoid reaction |
D72824 | Basophilia |
D72825 | Bandemia |
D72828 | Other elevated white blood cell count |
D72829 | Elevated white blood cell count, unspecified |
D7289 | Other specified disorders of white blood cells |
D729 | Disorder of white blood cells, unspecified |
D7381 | Neutropenic splenomegaly |
D7581 | Myelofibrosis |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D761 | Hemophagocytic lymphohistiocytosis |
D762 | Hemophagocytic syndrome, infection-associated |
D763 | Other histiocytosis syndromes |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 0505 |
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 |
D721 | Eosinophilia |
D72810 | Lymphocytopenia |
D72818 | Other decreased white blood cell count |
D72819 | Decreased white blood cell count, unspecified |
D72820 | Lymphocytosis (symptomatic) |
D72821 | Monocytosis (symptomatic) |
D72822 | Plasmacytosis |
D72823 | Leukemoid reaction |
D72824 | Basophilia |
D72825 | Bandemia |
D72828 | Other elevated white blood cell count |
D72829 | Elevated white blood cell count, unspecified |
D7289 | Other specified disorders of white blood cells |
D729 | Disorder of white blood cells, unspecified |
D7381 | Neutropenic splenomegaly |
D7581 | Myelofibrosis |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D761 | Hemophagocytic lymphohistiocytosis |
D762 | Hemophagocytic syndrome, infection-associated |
D763 | Other histiocytosis syndromes |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 0506 |
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 |
D591 | Other autoimmune hemolytic anemias |
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 0507 |
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 |
D7582 | Heparin induced thrombocytopenia (HIT) |
D759 | Disease of blood and blood-forming organs, unspecified |
|
PDX Collection 0508 |
D7801 | Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen |
D7802 | Intraoperative hemorrhage and hematoma of the spleen complicating other procedure |
D7821 | Postprocedural hemorrhage of the spleen following a procedure on the spleen |
D7822 | Postprocedural hemorrhage of the spleen following other procedure |
D7831 | Postprocedural hematoma of the spleen following a procedure on the spleen |
D7832 | Postprocedural hematoma of the spleen following other procedure |
D7833 | Postprocedural seroma of the spleen following a procedure on the spleen |
D7834 | Postprocedural seroma of the spleen following other procedure |
D7881 | Other intraoperative complications of the spleen |
D7889 | Other postprocedural complications of the spleen |
H95811 | Postprocedural stenosis of right external ear canal |
H95812 | Postprocedural stenosis of left external ear canal |
H95813 | Postprocedural stenosis of external ear canal, bilateral |
H95819 | Postprocedural stenosis of unspecified external ear canal |
H9588 | Other intraoperative complications and disorders of the ear and mastoid process, not elsewhere classified |
H9589 | Other postprocedural complications and disorders of the ear and mastoid process, not elsewhere classified |
I8501 | Esophageal varices with bleeding |
I8511 | Secondary esophageal varices with bleeding |
I973 | Postprocedural hypertension |
K219 | Gastro-esophageal reflux disease without esophagitis |
K228 | Other specified diseases of esophagus |
K23 | Disorders of esophagus in diseases classified elsewhere |
K250 | Acute gastric ulcer with hemorrhage |
K252 | Acute gastric ulcer with both hemorrhage and perforation |
K254 | Chronic or unspecified gastric ulcer with hemorrhage |
K256 | Chronic or unspecified gastric ulcer with both hemorrhage and perforation |
K260 | Acute duodenal ulcer with hemorrhage |
K262 | Acute duodenal ulcer with both hemorrhage and perforation |
K264 | Chronic or unspecified duodenal ulcer with hemorrhage |
K266 | Chronic or unspecified duodenal ulcer with both hemorrhage and perforation |
K270 | Acute peptic ulcer, site unspecified, with hemorrhage |
K272 | Acute peptic ulcer, site unspecified, with both hemorrhage and perforation |
K274 | Chronic or unspecified peptic ulcer, site unspecified, with hemorrhage |
K276 | Chronic or unspecified peptic ulcer, site unspecified, with both hemorrhage and perforation |
K280 | Acute gastrojejunal ulcer with hemorrhage |
K282 | Acute gastrojejunal ulcer with both hemorrhage and perforation |
K284 | Chronic or unspecified gastrojejunal ulcer with hemorrhage |
K286 | Chronic or unspecified gastrojejunal ulcer with both hemorrhage and perforation |
K2901 | Acute gastritis with bleeding |
K2921 | Alcoholic gastritis with bleeding |
K2931 | Chronic superficial gastritis with bleeding |
K2941 | Chronic atrophic gastritis with bleeding |
K2951 | Unspecified chronic gastritis with bleeding |
K2961 | Other gastritis with bleeding |
K2971 | Gastritis, unspecified, with bleeding |
K2981 | Duodenitis with bleeding |
K2991 | Gastroduodenitis, unspecified, with bleeding |
K31811 | Angiodysplasia of stomach and duodenum with bleeding |
K5521 | Angiodysplasia of colon with hemorrhage |
K5701 | Diverticulitis of small intestine with perforation and abscess with bleeding |
K5711 | Diverticulosis of small intestine without perforation or abscess with bleeding |
K5713 | Diverticulitis of small intestine without perforation or abscess with bleeding |
K5721 | Diverticulitis of large intestine with perforation and abscess with bleeding |
K5731 | Diverticulosis of large intestine without perforation or abscess with bleeding |
K5733 | Diverticulitis of large intestine without perforation or abscess with bleeding |
K5741 | Diverticulitis of both small and large intestine with perforation and abscess with bleeding |
K5751 | Diverticulosis of both small and large intestine without perforation or abscess with bleeding |
K5753 | Diverticulitis of both small and large intestine without perforation or abscess with bleeding |
K5781 | Diverticulitis of intestine, part unspecified, with perforation and abscess with bleeding |
K5791 | Diverticulosis of intestine, part unspecified, without perforation or abscess with bleeding |
K5793 | Diverticulitis of intestine, part unspecified, without perforation or abscess with bleeding |
K625 | Hemorrhage of anus and rectum |
K920 | Hematemesis |
K921 | Melena |
K922 | Gastrointestinal hemorrhage, unspecified |
M9689 | Other intraoperative and postprocedural complications and disorders of the musculoskeletal system |
N981 | Hyperstimulation of ovaries |
N982 | Complications of attempted introduction of fertilized ovum following in vitro fertilization |
N983 | Complications of attempted introduction of embryo in embryo transfer |
N988 | Other complications associated with artificial fertilization |
N989 | Complication associated with artificial fertilization, unspecified |
P541 | Neonatal melena |
P542 | Neonatal rectal hemorrhage |
P543 | Other neonatal gastrointestinal hemorrhage |
T8110XA | Postprocedural shock unspecified, initial encounter |
T8111XA | Postprocedural cardiogenic shock, initial encounter |
T8112XA | Postprocedural septic shock, initial encounter |
T8119XA | Other postprocedural shock, initial encounter |
T8182XA | Emphysema (subcutaneous) resulting from a procedure, initial encounter |
T8189XA | Other complications of procedures, not elsewhere classified, initial encounter |
T819XXA | Unspecified complication of procedure, initial encounter |
|
PDX Collection 0509 |
D7811 | Accidental puncture and laceration of the spleen during a procedure on the spleen |
D7812 | Accidental puncture and laceration of the spleen during other procedure |
D7881 | Other intraoperative complications of the spleen |
D7889 | Other postprocedural complications of the spleen |
E3611 | Accidental puncture and laceration of an endocrine system organ or structure during an endocrine system procedure |
E3612 | Accidental puncture and laceration of an endocrine system organ or structure during other procedure |
E368 | Other intraoperative complications of endocrine system |
E89810 | Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure |
E89811 | Postprocedural hemorrhage of an endocrine system organ or structure following other procedure |
E89820 | Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure |
E89821 | Postprocedural hematoma of an endocrine system organ or structure following other procedure |
E89822 | Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure |
E89823 | Postprocedural seroma of an endocrine system organ or structure following other procedure |
E8989 | Other postprocedural endocrine and metabolic complications and disorders |
G9611 | Dural tear |
G9741 | Accidental puncture or laceration of dura during a procedure |
G9748 | Accidental puncture and laceration of other nervous system organ or structure during a nervous system procedure |
G9749 | Accidental puncture and laceration of other nervous system organ or structure during other procedure |
H59011 | Keratopathy (bullous aphakic) following cataract surgery, right eye |
H59012 | Keratopathy (bullous aphakic) following cataract surgery, left eye |
H59013 | Keratopathy (bullous aphakic) following cataract surgery, bilateral |
H59019 | Keratopathy (bullous aphakic) following cataract surgery, unspecified eye |
H59031 | Cystoid macular edema following cataract surgery, right eye |
H59032 | Cystoid macular edema following cataract surgery, left eye |
H59033 | Cystoid macular edema following cataract surgery, bilateral |
H59039 | Cystoid macular edema following cataract surgery, unspecified eye |
H59091 | Other disorders of the right eye following cataract surgery |
H59092 | Other disorders of the left eye following cataract surgery |
H59093 | Other disorders of the eye following cataract surgery, bilateral |
H59099 | Other disorders of unspecified eye following cataract surgery |
H59211 | Accidental puncture and laceration of right eye and adnexa during an ophthalmic procedure |
H59212 | Accidental puncture and laceration of left eye and adnexa during an ophthalmic procedure |
H59213 | Accidental puncture and laceration of eye and adnexa during an ophthalmic procedure, bilateral |
H59219 | Accidental puncture and laceration of unspecified eye and adnexa during an ophthalmic procedure |
H59221 | Accidental puncture and laceration of right eye and adnexa during other procedure |
H59222 | Accidental puncture and laceration of left eye and adnexa during other procedure |
H59223 | Accidental puncture and laceration of eye and adnexa during other procedure, bilateral |