Opportunities for Engaging Long-Term and Post-Acute Care Providers in Health Information Exchange Activities: Exchanging Interoperable Patient Assessment Information. Anemia

12/01/2011

(Excel file available at: http://aspe.hhs.gov/daltcp/reports/2011/SE-D/AnemiaFindings.xls)

Refset Name: Anemia findings refset
  refset_ID   SCTID FSN
806 183005 Autoimmune pancytopenia (disorder)
806 1.27E+08 Pancytopenia (disorder)
806 359007 Kernicterus due to isoimmunization (disorder)
806 2.34E+08 Neonatal anemia (disorder)
806   3.88E+08 Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)
806 862001 Anemia due to chlorates (disorder)
806 4.25E+08 Anemia due to substance (disorder)
806 934007 Thalassemia intermedia (disorder)
806 40108008 Thalassemia (disorder)
806 1.27E+08 Paroxysmal cold hemoglobinuria (disorder)
806 3.99E+08 Cold autoimmune hemolytic anemia (disorder)
806 1963002 Paroxysmal nocturnal hemoglobinuria (disorder)
806 3.24E+08 Anemia due to intrinsic red cell abnormality (disorder)
806 2694001 Myelophthisic anemia (disorder)
806 2.72E+08 Anemia (disorder)
806 2835000 Traumatic cardiac hemolytic anemia (disorder)
806 34247008 Anemia due to mechanical damage (disorder)
806 1.91E+08 Aplastic anemia due to radiation (disorder)
806 3272007 Stomatocytosis (disorder)
806 3571004 Megaloblastic anemia due to pancreatic insufficiency (disorder)
806 53165003 Megaloblastic anemia (disorder)
806 3978000 Warm autoimmune hemolytic anemia (disorder)
806 4.14E+08 Autoimmune hemolytic anemia (disorder)
806 4854004 Acquired hemolytic anemia (disorder)
806 61261009 Hemolytic anemia (disorder)
806 4939006 Hemolytic anemia due to nonlymphoid neoplasm (disorder)
806 4984008 Microcytic normochromic anemia (disorder)
806 2.34E+08 Microcytic anemia (disorder)
806 5300004 Hemoglobin Bart's hydrops syndrome (disorder)
806 68913001 alpha Thalassemia (disorder)
806 5315003 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to increased adenosine deaminase activity (disorder)
806 3.01E+08 Hereditary nonspherocytic hemolytic anemia (disorder)
806 5430006 Megaloblastic anemia due to total parenteral nutrition (disorder)
806 5603006 Autoimmune hemolytic anemia due to IgG (disorder)
806 1.27E+08 Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement (disorder)
806 5876000 Acquired pancytopenia (disorder)
806 5967006 A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis (disorder)
806 39586009 Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia (disorder)
806 5994005 Hereditary elliptocytosis due to deficiency of protein 4.1 (disorder)
806 6398009 Idiopathic chronic cold agglutinin disease (disorder)
806 1.27E+08 Chronic cold agglutinin disease (disorder)
806 22098000 Chronic idiopathic autoimmune hemolytic anemia (disorder)
806 3.6E+08 Familial megaloblastic anemia (disorder)
806 2.34E+08 Selective malabsorption of cyanocobalamin (disorder)
806 6659005 Megaloblastic anemia due to nontropical sprue (disorder)
806 82895008 Megaloblastic anemia due to disease of small intestine (disorder)
806 8857001 Hereditary elliptocytosis due to alpha spectrin defect (disorder)
806 2.68E+08 Aplastic anemia due to drugs (disorder)
806 9364004 Feline infectious anemia (disorder)
806 4.22E+08 Mycoplasmal anemia (disorder)
806 1.12E+08 Anemia due to infection (disorder)
806 9434008 Hereditary pyropoikilocytosis (disorder)
806 9764001 Anemia due to radiation (disorder)
806 1.12E+08 Anemia due to physical agent (disorder)
806 10205009 Megaloblastic anemia due to exfoliative dermatitis (disorder)
806 10564005 Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)
806 47516005 Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)
806 10619002 Megaloblastic anemia due to poor nutrition (disorder)
806 11491000 Anemia due to niacin deficiency (disorder)
806 52565000 Non megaloblastic anemia associated with nutritional deficiency (disorder)
806 11503009 Relative anemia (disorder)
806 1.27E+08 Hereditary hemoglobinopathy disorder homozygous for hemoglobin S (disorder)
806 11781007 Autoimmune hemolytic anemia due to complement (disorder)
806 12109003 Hemolytic anemia associated with ulcerative colitis (disorder)
806 18889005 Hemolytic anemia associated with chronic inflammatory disease (disorder)
806 12189000 Coombs negative hemolytic anemia (disorder)
806 12238007 Megaloblastic anemia due to gastrectomy (disorder)
806 1.11E+08 Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization (disorder)
806 12907000 Thiamine-responsive megaloblastic anemia (disorder)
806 34925000 Megaloblastic anemia due to inborn errors of metabolism (disorder)
806 14024008 Humoral immunologic aplastic anemia (disorder)
806 77084001 Immunologic aplastic anemia (disorder)
806 14087004 Hereditary stomatocytosis (disorder)
806 14126008 Autosomal-linked pyridoxine refractory sideroblastic anemia (disorder)
806 41841004 Sideroblastic anemia (disorder)
806 14379009 Dimorphic anemia (disorder)
806 45098004 Anemia due to multiple mechanisms (disorder)
806 14514008 Anemia due to disturbance of hemoglobin synthesis (disorder)
806 15121005 Hereditary elliptocytosis due to glycophorin C deficiency (disorder)
806 15276008 Drug-induced enzyme deficiency anemia (disorder)
806 1.12E+08 Anemia due to enzyme deficiency (disorder)
806 4.28E+08 Anemia due to medication (disorder)
806 15326009 beta^+^ Thalassemia, normal Hb A>2<, type 2 (disorder)
806 79592006 beta^+^ Thalassemia (disorder)
806 15332004 Goats' milk anemia (disorder)
806 15539009 Hydrops fetalis due to isoimmunization (disorder)
806 16360009 delta beta Thalassemia (disorder)
806 65959000 beta Thalassemia (disorder)
806 16427007 delta Thalassemia (disorder)
806 16645003 Anemia due to insect venoms (disorder)
806 16964007 Hereditary persistence of fetal hemoglobin thalassemia (disorder)
806 2.4E+08 Oroya fever (disorder)
806 18273004 Unstable hemoglobin disease (disorder)
806 63565007 Congenital anemia (disorder)
806 18323000 Drug-induced immune hemolytic anemia, immune complex type (disorder)
806 1.27E+08 Drug-induced immune hemolytic anemia (disorder)
806 18637002 Megaloblastic anemia of premature infant (disorder)
806 66612000 Nutritional anemia (disorder)
806 18662002 Acquired Heinz body anemia (disorder)
806 1.27E+08 Secondary autoimmune hemolytic anemia (disorder)
806 19442009 Heterozygous thalassemia (disorder)
806 21412009 X chromosome-linked pyridoxine refractory sideroblastic anemia (disorder)
806 62677000 Hereditary sideroblastic anemia (disorder)
806 21914002 Anemia of thyroid dysfunction (disorder)
806 31820007 Anemia of endocrine disorder (disorder)
806 4.16E+08 Hemoglobin SS disease without crisis (disorder)
806 1.27E+08 Primary (idiopathic) autoimmune hemolytic anemia (disorder)
806 1.91E+08 Chronic anemia (disorder)
806 22347002 Anemia of gonadal dysfunction (disorder)
806 59106005 Anemia due to decreased red cell production (disorder)
806 22438006 Anemia due to disturbance of proliferation AND/OR differentiation of hematopoietic stem cells (disorder)
806 22933009 G-6-PD class I variant anemia (disorder)
806 62403005 Glucose-6-phosphate dehydrogenase deficiency anemia (disorder)
806 23371004 epsilon gamma delta beta Thalassemia (disorder)
806 24620004 Hemolytic anemia due to babesiosis (disorder)
806 38689004 Hemolytic anemia due to infection (disorder)
806 24661004 G-6-PD class III variant anemia (disorder)
806 24962009 Anemia due to vitamin E deficiency (disorder)
806 24975009 Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)
806 32648007 Mild hereditary spherocytosis due to spectrin deficiency (disorder)
806 25251008 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to gamma glutamyl cysteine synthetase deficiency (disorder)
806 25266006 Hereditary spherocytosis due to spectrin deficiency (disorder)
806 55995005 Hereditary spherocytosis (disorder)
806 25443007 X chromosome-linked pyridoxine responsive sideroblastic anemia (disorder)
806 26333003 Megaloblastic anemia due to vitamin B>12< malabsorption with proteinuria (disorder)
806 26409005 Congenital dyserythropoietic anemia, type III (disorder)
806 52951008 Congenital dyserythropoietic anemia (disorder)
806 26682008 Homozygous beta thalassemia (disorder)
806 26944003 Acute megaloblastic anemia due to dialysis (disorder)
806 82430007 Acute megaloblastic anemia (disorder)
806 27080008 beta^0^ Thalassemia, deletion type (disorder)
806 86715000 beta^0^ Thalassemia (disorder)
806 27342004 Anemia of pregnancy (disorder)
806 45828008 Anemia in mother complicating pregnancy, childbirth AND/OR puerperium (disorder)
806 27366005 Megaloblastic anemia due to hemodialysis (disorder)
806 27798002 Megaloblastic anemia due to impaired absorption of folate (disorder)
806 85649008 Megaloblastic anemia due to folate deficiency (disorder)
806 28147001 Hemolytic anemia due to Clostridium welchii (disorder)
806 28975000 Constitutional aplastic anemia (disorder)
806 3.06E+08 Aplastic anemia (disorder)
806 29177004 Anemia due to pentose phosphate pathway defect (disorder)
806 29551000 Anemia due to oxygen (disorder)
806 30418008 Anemia of adrenal dysfunction (disorder)
806 30575002 Fanconi's anemia (disorder)
806 31206006 Refractory megaloblastic anemia (disorder)
806 4.14E+08 Aplastic anemia associated with pancreatitis (disorder)
806 32094009 Megaloblastic anemia due to fish tapeworm (disorder)
806 32855007 Hereditary persistence of fetal hemoglobin (HPF) unlinked to beta-globulin gene cluster (disorder)
806 32858009 Hemolytic disease of fetus OR newborn due to ABO immunization (disorder)
806 3.88E+08 Perinatal anemia (disorder)
806 33491002 Autoimmune hemolytic anemia due to IgA plus complement (disorder)
806 91411007 Autoimmune hemolytic anemia due to IgA (disorder)
806 33905008 Hereditary spherocytosis due to deficiency of protein 4.2 (disorder)
806 34194007 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to pyrimidine-5'-nucleotidase deficiency (disorder)
806 44288006 Anemia due to abnormality extrinsic to the red cell (disorder)
806 34629009 Anemia due to zinc deficiency (disorder)
806 34852006 G-6-PD class II variant anemia (disorder)
806 4.21E+08 Anemia associated with AIDS (disorder)
806 35703006 Post-viral paroxysmal cold hemoglobinuria (disorder)
806 35778001 Megaloblastic anemia due to error of folate metabolism (disorder)
806 4.21E+08 Deficiency anemia associated with AIDS (disorder)
806 36467003 alpha^+^ Thalassemia (disorder)
806 36472007 Sickle cell-thalassemia disease (disorder)
806 47047009 Thalassemia with other hemoglobinopathy (disorder)
806 36568005 Hemolytic uremic syndrome of childhood (disorder)
806 1.11E+08 Hemolytic uremic syndrome (disorder)
806 36919001 Anemia due to lead (disorder)
806 37272000 Rh deficiency syndrome (disorder)
806 37370005 Megaloblastic anemia due to drugs (disorder)
806 3.1E+08 Drug-induced autoimmune hemolytic anemia (disorder)
806 38911009 Hereditary hemolytic anemia (disorder)
806 38970002 Doan-Wright syndrome (disorder)
806 40387008 Polyagglutinable erythrocyte syndrome (disorder)
806 66309005 Antibody-mediated anemia (disorder)
806 41387000 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphofructokinase deficiency (disorder)
806 41462006 Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells (disorder)
806 41614006 Hypoplastic anemia (disorder)
806 42461002 Anemia due to copper (disorder)
806 42484009 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency (disorder)
806 1.91E+08 Hemolytic anemia due to hexokinase deficiency (disorder)
806 42601008 Congenital hemolytic anemia (disorder)
806 4.14E+08 Anemia due to chronic blood loss (disorder)
806 2.68E+08 Acute posthemorrhagic anemia (disorder)
806 43707008 Anemia due to heat (disorder)
806 43858000 Secondary aplastic anemia (disorder)
806 44206008 Hapten type low affinity hemolytic anemia (disorder)
806 1.27E+08 Drug-induced immune hemolytic anemia, hapten type (disorder)
806 44452003 Normocytic hypochromic anemia (disorder)
806 44641000 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency (disorder)
806 44666001 Microcytic hypochromic anemia (disorder)
806 44910003 Megaloblastic anemia due to decreased intake of vitamin B>12< (disorder)
806 84027009 Pernicious anemia (disorder)
806 46737006 Normocytic normochromic anemia (disorder)
806 46760003 Estren-Dameshek anemia (disorder)
806 47084006 beta^+^ Thalassemia, normal Hb A>2<, type 1, silent (disorder)
806 47100003 Anemia of prematurity (disorder)
806 4.14E+08 Aplastic anemia associated with pregnancy (disorder)
806 47526003 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency (disorder)
806 47844003 Megaloblastic anemia due to chronic hemolytic anemia (disorder)
806 48553001 Hemoglobin H disease (disorder)
806 48580008 Anemia due to starvation (disorder)
806 1.91E+08 Aplastic anemia due to toxic cause (disorder)
806 49284006 Juvenile type megaloblastic anemia (disorder)
806 49472006 Megaloblastic anemia due to vitamin B>12< deficiency (disorder)
806 1.91E+08 Combined B12 and folate deficiency anemia (disorder)
806 49708008 Anemia of chronic renal failure (disorder)
806 2.34E+08 Anemia of chronic disorder (disorder)
806 3.11E+08 Anemia secondary to renal failure (disorder)
806 50220002 Cellular immunologic aplastic anemia (disorder)
806 50253007 Secondary paroxysmal cold hemoglobinuria (disorder)
806 50715003 Pure red cell aplasia (disorder)
806 51071000 Microangiopathic hemolytic anemia (disorder)
806 51667002 Anemia due to riboflavin deficiency (disorder)
806 52212006 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glutathione reductase deficiency (disorder)
806 52413004 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glucose phosphate isomerase deficiency (disorder)
806 2.68E+08 Deficiency anemias (disorder)
806 83414005 Macrocytic anemia (disorder)
806 1.06E+08 Anemia related to disturbed DNA synthesis (disorder)
806 53743006 Anemia following fetal blood loss (disorder)
806 4.14E+08 Anemia due to blood loss (disorder)
806 54006005 Hereditary persistence of fetal hemoglobin (HPFH) delta beta^0^ thalassemia (disorder)
806 76336008 delta beta^0^ Thalassemia (disorder)
806 54698001 Megaloblastic anemia due to Zollinger-Ellison syndrome (disorder)
806 3.23E+08 Intracorpuscular hemolytic anemia (disorder)
806 55907008 Acquired aplastic anemia (disorder)
806 1.12E+08 Anemia due to membrane defect (disorder)
806 56205004 Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type (disorder)
806 1.91E+08 Folate deficiency anemia, drug-induced (disorder)
806 57192008 Acute pure red cell aplasia (disorder)
806 59548005 Congenital dyserythropoietic anemia, type I (disorder)
806 59644002 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphoglycerate kinase deficiency (disorder)
806 60138009 Anemia of pituitary deficiency (disorder)
806 60164003 Megaloblastic anemia due to blind loop syndrome (disorder)
806 60504009 Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder)
806 2.34E+08 Congenital deficiency of intrinsic factor (disorder)
806 60805002 Hemolytic anemia with emphysema AND cutis laxa (disorder)
806 61395005 Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia (disorder)
806 61777009 Thalassemia-hemoglobin C disease (disorder)
806 62074008 delta^0^ Thalassemia (disorder)
806 62268000 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to diphosphoglycerate mutase deficiency (disorder)
806 62389006 Acute megaloblastic anemia due to severe illness (disorder)
806 62609001 Autoimmune hemolytic anemia due to IgG plus complement (disorder)
806 62871001 Idiopathic paroxysmal cold hemoglobinuria (disorder)
806 65560000 Amino acid deficiency anemia (disorder)
806 1.91E+08 Protein-deficiency anemia (disorder)
806 66055002 alpha^0^ Thalassemia (disorder)
806 66184009 Hemolytic anemia associated with lymphoproliferative disorder (disorder)
806 66262001 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder)
806 1.91E+08 Aplastic anemia due to chronic disease (disorder)
806 1.91E+08 Vitamin C deficiency anemia (disorder)
806 67894009 Megaloblastic anemia due to increased requirements (disorder)
806 4.22E+08 Acquired hemolytic anemia associated with AIDS (disorder)
806 68361004 Late anemia due to isoimmunization (disorder)
806 68700003 Megaloblastic anemia due to error of cobalamin metabolism (disorder)
806 68870007 Congenital dyserythropoietic anemia, type II (disorder)
806 2.69E+08 Beta thalassemia trait (disorder)
806 69216008 Hb Lepore thalassemia (disorder)
806 4.14E+08 Aplastic anemia associated with metabolic alteration (disorder)
806 69574002 Anemia of parathyroid dysfunction (disorder)
806 69746005 Hemolytic anemia associated with systemic lupus erythematosus (disorder)
806 1.12E+08 Hemolytic anemia associated with rheumatic disorder (disorder)
806 69981004 Hereditary spherocytosis due to beta spectrin defect (disorder)
806 70517008 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methemoglobin reductase deficiency (disorder)
806 71832003 Autoimmune hemolytic anemia due to IgM (disorder)
806 71855000 Acute megaloblastic anemia secondary to total parenteral nutrition (disorder)
806 4.17E+08 Hemoglobin SS disease with crisis (disorder)
806 72501006 Anemia due to arsenic hydride (disorder)
806 73073009 Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder)
806 73190000 epsilon gamma delta beta^0^ Thalassemia (disorder)
806 73891003 Acute megaloblastic anemia due to nitrous oxide (disorder)
806 74703006 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to pyruvate kinase deficiency (disorder)
806 74789008 Coombs positive hemolytic anemia (disorder)
806 75331009 Evans syndrome (disorder)
806 75443009 Hereditary elliptocytosis due to abnormal protein 4.1 (disorder)
806 75451007 Thalassemia major (disorder)
806 2.9E+08 Sideropenic anemia with reticuloendothelial siderosis (disorder)
806 2.91E+08 Simple chronic anemia (disorder)
806 3.71E+08 Iron deficiency anemia secondary to inadequate dietary iron intake (disorder)
806 76366001 Hemolytic anemia due to Bartonella (disorder)
806 77413008 Severe hereditary spherocytosis due to spectrin deficiency (disorder)
806 77607006 Drug-induced sideroblastic anemia (disorder)
806 90175006 Secondary acquired sideroblastic anemia (disorder)
806 77663007 Hemolytic anemia due to malaria (disorder)
806 78129009 Thrombotic thrombocytopenic purpura (disorder)
806 78209002 Hemolytic uremic syndrome, adult type (disorder)
806 78677008 Anemia due to pantothenic deficiency (disorder)
806 78908001 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to decreased adenosine deaminase activity (disorder)
806 78997000 Megaloblastic anemia due to vegetarianism (disorder)
806 79035003 Anemia due to unknown mechanism (disorder)
806 80126007 Plummer-Vinson syndrome (disorder)
806 87522002 Iron deficiency anemia (disorder)
806 80875006 Achlorhydric anemia (disorder)
806 80963002 G-6-PD class V variant anemia (disorder)
806 81711008 Hemolytic anemia due to drugs (disorder)
806 82003006 G-6-PD class IV variant anemia (disorder)
806 82980005 Anemia of diabetes (disorder)
806 1.91E+08 Aplastic anemia due to infection (disorder)
806 4.21E+08 Aplastic anemia associated with AIDS (disorder)
806 84188003 Thalassemia syndrome (disorder)
806 85422000 alpha^+^ Thalassemia, nondeletion type (disorder)
806 85557000 Hereditary persistence of fetal hemoglobin (HPFH) deletion type (disorder)
806 85570009 Anemia due to vitamin A deficiency (disorder)
806 85746008 Anemia due to protein deficiency (disorder)
806 86225009 Hapten type high affinity hemolytic anemia (disorder)
806 86242003 alpha^+^ Thalassemia, deletion type (disorder)
806 86325007 Non megaloblastic anemia due to alcoholism (disorder)
806 86448001 Anemia due to vitamin B>6< deficiency (disorder)
806 86859003 G-6-PD variant enzyme deficiency anemia (disorder)
806 86986002 Hemolytic disease of fetus OR newborn due to RhD isoimmunization (disorder)
806 87190009 Infectious avian anemia (disorder)
806 87806008 Megaloblastic anemia due to tropical sprue (disorder)
806 87810006 Megaloblastic anemia due to alcoholism (disorder)
806 87994004 Xerocytosis (disorder)
806 88854002 Congenital hypoplastic anemia (disorder)
806 89112009 Aregenerative anemia (disorder)
806 89459006 Hereditary persistence of fetal hemoglobin (HPFH) linked to beta-globulin gene cluster (disorder)
806 89810003 ^A^gamma delta beta^0^ thalassemia (disorder)
806 90414007 Chronic acquired pure red cell aplasia (disorder)
806 2.34E+08 Acquired red cell aplasia (disorder)
806 91217009 Megaloblastic anemia due to pregnancy (disorder)
806 1.1E+08 Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts (disorder)
806 1.1E+08 Refractory anemia with ringed sideroblasts (disorder)
806 3.99E+08 Refractory anemia with excess blasts (disorder)
806 1.1E+08 Refractory anemia with excess blasts in transformation (disorder)
806 1.1E+08 Chicken anemia virus infection (disorder)
806 1.12E+08 Congenital atransferinemia (disorder)
806 1.12E+08 beta^0^ Thalassemia, nondeletion type (disorder)
806 1.12E+08 Anemia due to unknown or multiple mechanisms (disorder)
806 1.12E+08 Anemia due to copper deficiency (disorder)
806 1.12E+08 Acquired stomatocytosis (disorder)
806 1.12E+08 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to aldolase A deficiency (disorder)
806 1.12E+08 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glutathione synthetase deficiency (disorder)
806 3.88E+08 Sports anemia (disorder)
806 1.16E+08 Regenerative anemia (disorder)
806 1.27E+08 Sickle cell-beta-thalassemia (disorder)
806 1.27E+08 Sickle cell-beta^+^-thalassemia (disorder)
806 1.27E+08 Sickle cell-beta^0^-thalassemia (disorder)
806 1.27E+08 Sickle cell-delta beta^0^-thalassemia (disorder)
806 1.27E+08 Sickle cell anemia with coexistent alpha-thalassemia (disorder)
806 1.27E+08 Sickle cell trait with coexistent alpha-thalassemia (disorder)
806 1.27E+08 Primary (idiopathic) warm autoimmune hemolytic anemia (disorder)
806 1.27E+08 Secondary warm autoimmune hemolytic anemia (disorder)
806 1.27E+08 Post-infectious cold agglutinin disease (disorder)
806 1.27E+08 Cold agglutinin disease due to Epstein-Barr virus infection (disorder)
806 1.27E+08 Chronic cold agglutinin disease associated with B-cell neoplasm (disorder)
806 1.27E+08 Paroxysmal cold hemoglobinuria associated with tertiary syphilis (disorder)
806 1.27E+08 Anemia due to alloimmune destruction of transfused red cells (disorder)
806 1.3E+08 Hemolytic anemia due to hyperbaric oxygen (disorder)
806 1.64E+08 On examination - equivocally anemic (disorder)
806 1.64E+08 On examination - clinically anemic (disorder)
806 1.64E+08 On examination - profoundly anemic (disorder)
806 2.87E+08 Deficiency anemias, excluding iron (disorder)
806 1.91E+08 Alpha trait thalassemia (disorder)
806 1.91E+08 Non-autoimmune hemolytic anemia (disorder)
806 2.74E+08 Anemia due to isoimmunization (disorder)
806 1.9E+08 Refractory anemia without sideroblasts, so stated (disorder)
806 1.91E+08 Severe combined immunodefiency with reticular dysgenesis (disorder)
806 2.34E+08 Normocytic anemia due to chronic blood loss (disorder)
806 1.91E+08 Iron deficiency anemia due to dietary causes (disorder)
806 1.91E+08 Chlorotic anemia (disorder)
806 1.91E+08 Idiopathic hypochromic anemia (disorder)
806 2.34E+08 Biermer's congenital pernicious anemia (disorder)
806 2.34E+08 Vegan's anemia (disorder)
806 2.68E+08 Vitamin B12 deficiency anemia due to dietary causes (disorder)
806 1.91E+08 Vitamin B12 deficiency anemia due to malabsorption with proteinuria (disorder)
806 1.91E+08 Congenital folate malabsorption anemia (disorder)
806 2.68E+08 Folate deficiency anemia due to dietary causes (disorder)
806 2.34E+08 Megaloblastic anemia due to dietary causes (disorder)
806 1.91E+08 Folate deficiency anemia due to malabsorption (disorder)
806 1.91E+08 Folate deficiency anemia due to liver disorders (disorder)
806 1.91E+08 Vitamin E deficiency anemia (disorder)
806 1.91E+08 Hemolytic anemia due to glutathione metabolism disorder (disorder)
806 1.91E+08 Hemolytic anemia due to pyruvate kinase deficiency (disorder)
806 1.91E+08 Hemolytic anemia due to triose phosphate isomerase deficiency (disorder)
806 1.91E+08 Anemia due to disorders of nucleotide metabolism (disorder)
806 2.34E+08 Homozygous alpha thalassemia (disorder)
806 1.91E+08 Beta thalassemia intermedia (disorder)
806 1.91E+08 Primary cold-type hemolytic anemia (disorder)
806 1.91E+08 Primary warm-type hemolytic anemia (disorder)
806 1.91E+08 Secondary cold-type hemolytic anemia (disorder)
806 1.91E+08 Secondary warm-type hemolytic anemia (disorder)
806 1.91E+08 Mechanical hemolytic anemia (disorder)
806 1.91E+08 Toxic hemolytic anemia (disorder)
806 1.91E+08 Infective hemolytic anemia (disorder)
806 1.91E+08 Hemoglobinuria due to hemolysis from external causes (disorder)
806 1.91E+08 Acquired spherocytosis (disorder)
806 1.91E+08 Pyknocytosis, infantile (disorder)
806 2.68E+08 Constitutional aplastic anemia with malformation (disorder)
806 2.76E+08 Pancytopenia-dysmelia (disorder)
806 2.68E+08 Constitutional red cell aplasia and hypoplasia (disorder)
806 2.34E+08 Congenital red cell hypoplasia (disorder)
806 2.34E+08 Constitutional red cell hypoplasia (disorder)
806 2.34E+08 Congenital pure red cell aplasia (disorder)
806 1.91E+08 Erythrogenesis imperfecta (disorder)
806 2.34E+08 Normocytic anemia due to aplasia (disorder)
806 2.34E+08 Pancytopenia with pancreatitis (disorder)
806 1.91E+08 Transient hypoplastic anemia (disorder)
806 2.34E+08 Pure red cell aplasia, acquired (disorder)
806 1.91E+08 Transient acquired pure red cell aplasia (disorder)
806 1.91E+08 Idiopathic aplastic anemia (disorder)
806 1.91E+08 Pyridoxine-responsive sideroblastic anemia (disorder)
806 1.91E+08 Secondary sideroblastic anemia due to disease (disorder)
806 1.91E+08 Secondary sideroblastic anemia due to drugs and toxins (disorder)
806 3.03E+08 Normocytic anemia following acute bleed (disorder)
806 1.91E+08 Anemia in neoplastic disease (disorder)
806 3.08E+08 Anemia in ovarian carcinoma (disorder)
806 1.99E+08 Anemia during pregnancy - baby delivered (disorder)
806 1.99E+08 Anemia in the puerperium - baby delivered during current episode of care (disorder)
806 3.13E+08 Anemia during the puerperium (disorder)
806 1.99E+08 Anemia during pregnancy - baby not yet delivered (disorder)
806 1.99E+08 Anemia in the puerperium - baby delivered during previous episode of care (disorder)
806 1.99E+08 Iron deficiency anemia of pregnancy (disorder)
806 2.06E+08 Late anemia of newborn due to isoimmunization (disorder)
806 2.77E+08 Late anemia of newborn (disorder)
806 2.07E+08 Congenital anemia from fetal blood loss (disorder)
806 3.01E+08 Normocytic anemia (disorder)
806 2.34E+08 Dilutional anemia (disorder)
806 2.34E+08 Anemia of renal disease (disorder)
806 2.34E+08 Congenital transferrin deficiency (disorder)
806 2.34E+08 Combined deficiency anemia (disorder)
806 2.34E+08 Thiamine-responsive macrocytosis (disorder)
806 2.34E+08 Alcohol-related sideroblastic anemia (disorder)
806 2.34E+08 Transient erythroblastopenia of childhood (disorder)
806 2.34E+08 Kell isoimmunization of the newborn (disorder)
806 2.34E+08 Maternal autoimmune hemolytic anemia (disorder)
806 2.34E+08 Alpha thalassemia-2 trait (disorder)
806 2.34E+08 Hemoglobin Constant Spring trait (disorder)
806 2.34E+08 Hemoglobin Lepore trait (disorder)
806 2.34E+08 Delta-beta-Lepore thalassemia (disorder)
806 2.34E+08 Alpha-beta thalassemia (disorder)
806 2.34E+08 Gamma thalassemia (disorder)
806 2.34E+08 Sickle cell anemia with high hemoglobin F (disorder)
806 2.38E+08 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder)
806 2.38E+08 Pearson's syndrome (disorder)
806 2.4E+08 Parvoviral aplastic crisis (disorder)
806 2.76E+08 Idiopathic sideroblastic anemia (disorder)
806 2.77E+08 Physiological anemia of infancy (disorder)
806 2.77E+08 Atypical isoimmunization of newborn (disorder)
806 2.78E+08 Alpha thalassemia-mental retardation syndrome (disorder)
806 2.78E+08 Alcoholic macrocytosis (disorder)
806 3.07E+08 Rhesus isoimmunization due to anti-D (disorder)
806 3.07E+08 Rhesus isoimmunization due to anti-c (disorder)
806 3.07E+08 Rhesus isoimmunization due to anti-E (disorder)
806 3.07E+08 Rhesus isoimmunization due to anti-Cw (disorder)
806 3.07E+08 Duffy isoimmunization of the newborn (disorder)
806 3.07E+08 Kidd isoimmunization of the newborn (disorder)
806 3.07E+08 Acquired hemoglobin H disease (disorder)
806 3.63E+08 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder)
806 3.71E+08 Traumatic hemolytic anemia (disorder)
806 3.73E+08 Upshaw-Schulman syndrome (disorder)
806 3.73E+08 Diarrhea-associated hemolytic uremic syndrome (disorder)
806 3.73E+08 Diarrhea-negative hemolytic uremic syndrome (disorder)
806 3.89E+08 Diaphyseal dysplasia with anemia (disorder)
806 4.15E+08 Refractory anemia with excess blasts-1 (disorder)
806 4.15E+08 Refractory anemia with excess blasts-2 (disorder)
806 4.17E+08 Sickle cell-thalassemia disease with crisis (disorder)
806 4.17E+08 Sickle cell-thalassemia disease without crisis (disorder)
806 4.3E+08 Anemia due to chemotherapy (disorder)
806 4.38E+08 Autoimmune thrombotic thrombocytopenic purpura (disorder)
806 4.39E+08 Acquired thrombotic thrombocytopenic purpura (disorder)
806 4.4E+08 Hemoglobin SS disease with vasoocclusive crisis (disorder)
806 4.41E+08 Drug induced thrombotic thrombocytopenic purpura (disorder)
806 4.44E+08 Acute sickle cell splenic sequestration crisis (disorder)
806 4.45E+08 Congenital hemolytic uremic syndrome (disorder)

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