Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)

  • Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) - D64.9 Anemia, unspecified
    • achlorhydric - D50.8 Other iron deficiency anemias
    • achrestic - D53.1 Other megaloblastic anemias, not elsewhere classified
    • Addison (-Biermer) (pernicious) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • agranulocytic - See: Agranulocytosis;
    • amino-acid-deficiency - D53.0 Protein deficiency anemia
    • aplastic - D61.9 Aplastic anemia, unspecified
      • congenital - D61.09 Other constitutional aplastic anemia
      • drug-induced - D61.1 Drug-induced aplastic anemia
      • due to
        • drugs - D61.1 Drug-induced aplastic anemia
        • external agents NEC - D61.2 Aplastic anemia due to other external agents
        • infection - D61.2 Aplastic anemia due to other external agents
        • radiation - D61.2 Aplastic anemia due to other external agents
      • idiopathic - D61.3 Idiopathic aplastic anemia
      • red cell (pure) - D60.9 Acquired pure red cell aplasia, unspecified
        • chronic - D60.0 Chronic acquired pure red cell aplasia
        • congenital - D61.01 Constitutional (pure) red blood cell aplasia
        • specified type NEC - D60.8 Other acquired pure red cell aplasias
        • transient - D60.1 Transient acquired pure red cell aplasia
      • specified type NEC - D61.89 Other specified aplastic anemias and other bone marrow failure syndromes
      • toxic - D61.2 Aplastic anemia due to other external agents
    • aregenerative
      • congenital - D61.09 Other constitutional aplastic anemia
    • asiderotic - D50.9 Iron deficiency anemia, unspecified
    • atypical (primary) - D64.9 Anemia, unspecified
    • Baghdad spring - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
    • Balantidium coli - A07.0 Balantidiasis
    • Biermer's (pernicious) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
      • acute - D62 Acute posthemorrhagic anemia
    • bothriocephalus - B70.0 Diphyllobothriasis
    • brickmaker's - B76.9 Hookworm disease, unspecified
    • cerebral - I67.89 Other cerebrovascular disease
    • childhood - D58.9 Hereditary hemolytic anemia, unspecified
    • chlorotic - D50.8 Other iron deficiency anemias
    • chronic
      • blood loss - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
      • hemolytic - D58.9 Hereditary hemolytic anemia, unspecified
        • idiopathic - D59.9 Acquired hemolytic anemia, unspecified
      • simple - D53.9 Nutritional anemia, unspecified
    • chronica congenita aregenerativa - D61.09 Other constitutional aplastic anemia
    • combined system disease NEC - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
      • due to dietary vitamin B12 deficiency - D51.3 Other dietary vitamin B12 deficiency anemia
    • complicating pregnancy, childbirth or puerperium - See: Pregnancy, complicated by (management affected by), anemia;
    • congenital - P61.4 Other congenital anemias, not elsewhere classified
      • aplastic - D61.09 Other constitutional aplastic anemia
      • due to isoimmunization NOS - P55.9 Hemolytic disease of newborn, unspecified
      • dyserythropoietic, dyshematopoietic - D64.4 Congenital dyserythropoietic anemia
      • following fetal blood loss - P61.3 Congenital anemia from fetal blood loss
      • Heinz body - D58.2 Other hemoglobinopathies
      • hereditary hemolytic NOS - D58.9 Hereditary hemolytic anemia, unspecified
      • pernicious - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
      • spherocytic - D58.0 Hereditary spherocytosis
    • Cooley's (erythroblastic) - D56.1 Beta thalassemia
    • cytogenic - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • deficiency - D53.9 Nutritional anemia, unspecified
      • 2, 3 diphosphoglycurate mutase - D55.2 Anemia due to disorders of glycolytic enzymes
      • 2, 3 PG - D55.2 Anemia due to disorders of glycolytic enzymes
      • 6 phosphogluconate dehydrogenase - D55.1 Anemia due to other disorders of glutathione metabolism
      • 6-PGD - D55.1 Anemia due to other disorders of glutathione metabolism
      • amino-acid - D53.0 Protein deficiency anemia
      • combined B12 and folate - D53.1 Other megaloblastic anemias, not elsewhere classified
      • enzyme - D55.9 Anemia due to enzyme disorder, unspecified
        • drug-induced (hemolytic) - D59.2 Drug-induced nonautoimmune hemolytic anemia
        • glucose-6-phosphate dehydrogenase (G6PD) - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
        • glycolytic - D55.2 Anemia due to disorders of glycolytic enzymes
        • nucleotide metabolism - D55.3 Anemia due to disorders of nucleotide metabolism
        • specified type NEC - D55.8 Other anemias due to enzyme disorders
      • erythrocytic glutathione - D55.1 Anemia due to other disorders of glutathione metabolism
      • folate - D52.9 Folate deficiency anemia, unspecified
        • dietary - D52.0 Dietary folate deficiency anemia
        • drug-induced - D52.1 Drug-induced folate deficiency anemia
      • folic acid - D52.9 Folate deficiency anemia, unspecified
        • dietary - D52.0 Dietary folate deficiency anemia
        • drug-induced - D52.1 Drug-induced folate deficiency anemia
      • G SH - D55.1 Anemia due to other disorders of glutathione metabolism
      • G6PD - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
      • GGS-R - D55.1 Anemia due to other disorders of glutathione metabolism
      • glucose-6-phosphate dehydrogenase - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
      • glutathione reductase - D55.1 Anemia due to other disorders of glutathione metabolism
      • glyceraldehyde phosphate dehydrogenase - D55.2 Anemia due to disorders of glycolytic enzymes
      • hexokinase - D55.2 Anemia due to disorders of glycolytic enzymes
      • iron - D50.9 Iron deficiency anemia, unspecified
        • secondary to blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
      • nutritional - D53.9 Nutritional anemia, unspecified
        • with
          • poor iron absorption - D50.8 Other iron deficiency anemias
          • specified deficiency NEC - D53.8 Other specified nutritional anemias
      • phosphofructo-aldolase - D55.2 Anemia due to disorders of glycolytic enzymes
      • phosphoglycerate kinase - D55.2 Anemia due to disorders of glycolytic enzymes
      • PK - D55.2 Anemia due to disorders of glycolytic enzymes
      • protein - D53.0 Protein deficiency anemia
      • pyruvate kinase - D55.2 Anemia due to disorders of glycolytic enzymes
      • transcobalamin II - D51.2 Transcobalamin II deficiency
      • triose-phosphate isomerase - D55.2 Anemia due to disorders of glycolytic enzymes
      • vitamin B12 NOS - D51.9 Vitamin B12 deficiency anemia, unspecified
        • dietary - D51.3 Other dietary vitamin B12 deficiency anemia
        • due to
          • intrinsic factor deficiency - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
          • selective vitamin B12 malabsorption with proteinuria - D51.1 Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
        • pernicious - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
        • specified type NEC - D51.8 Other vitamin B12 deficiency anemias
    • Diamond-Blackfan (congenital hypoplastic) - D61.01 Constitutional (pure) red blood cell aplasia
    • dibothriocephalus - B70.0 Diphyllobothriasis
    • dimorphic - D53.1 Other megaloblastic anemias, not elsewhere classified
    • diphasic - D53.1 Other megaloblastic anemias, not elsewhere classified
    • Diphyllobothrium (Dibothriocephalus) - B70.0 Diphyllobothriasis
    • due to (in) (with)
      • antineoplastic chemotherapy - D64.81 Anemia due to antineoplastic chemotherapy
      • blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • chemotherapy, antineoplastic - D64.81 Anemia due to antineoplastic chemotherapy
      • chronic disease classified elsewhere NEC - D63.8 Anemia in other chronic diseases classified elsewhere
      • chronic kidney disease - D63.1 Anemia in chronic kidney disease
      • deficiency
        • amino-acid - D53.0 Protein deficiency anemia
        • copper - D53.8 Other specified nutritional anemias
        • folate (folic acid) - D52.9 Folate deficiency anemia, unspecified
          • dietary - D52.0 Dietary folate deficiency anemia
          • drug-induced - D52.1 Drug-induced folate deficiency anemia
        • molybdenum - D53.8 Other specified nutritional anemias
        • protein - D53.0 Protein deficiency anemia
        • zinc - D53.8 Other specified nutritional anemias
      • dietary vitamin B12 deficiency - D51.3 Other dietary vitamin B12 deficiency anemia
      • disorder of
        • glutathione metabolism - D55.1 Anemia due to other disorders of glutathione metabolism
        • nucleotide metabolism - D55.3 Anemia due to disorders of nucleotide metabolism
      • drug - See Also: Table of Drugs and Chemicals; See: Anemia, by type;
      • end stage renal disease - D63.1 Anemia in chronic kidney disease
      • enzyme disorder - D55.9 Anemia due to enzyme disorder, unspecified
      • fetal blood loss - P61.3 Congenital anemia from fetal blood loss
      • fish tapeworm (D.latum) infestation - B70.0 Diphyllobothriasis
      • hemorrhage (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • impaired absorption - D50.9 Iron deficiency anemia, unspecified
      • loss of blood (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • myxedema - E03.9 Hypothyroidism, unspecified
      • Necator americanus - B76.1 Necatoriasis
      • prematurity - P61.2 Anemia of prematurity
      • selective vitamin B12 malabsorption with proteinuria - D51.1 Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
      • transcobalamin II deficiency - D51.2 Transcobalamin II deficiency
    • Dyke-Young type (secondary) (symptomatic) - D59.1 Other autoimmune hemolytic anemias
    • dyserythropoietic (congenital) - D64.4 Congenital dyserythropoietic anemia
    • dyshematopoietic (congenital) - D64.4 Congenital dyserythropoietic anemia
    • Egyptian - B76.9 Hookworm disease, unspecified
    • elliptocytosis - See: Elliptocytosis;
    • enzyme-deficiency, drug-induced - D59.2 Drug-induced nonautoimmune hemolytic anemia
    • epidemic - See Also: Ancylostomiasis; - B76.9 Hookworm disease, unspecified
    • erythroblastic
      • familial - D56.1 Beta thalassemia
      • newborn - See Also: Disease, hemolytic; - P55.9 Hemolytic disease of newborn, unspecified
      • of childhood - D56.1 Beta thalassemia
    • erythrocytic glutathione deficiency - D55.1 Anemia due to other disorders of glutathione metabolism
    • erythropoietin-resistant anemia (EPO resistant anemia) - D63.1 Anemia in chronic kidney disease
    • Faber's (achlorhydric anemia) - D50.9 Iron deficiency anemia, unspecified
    • factitious (self-induced blood letting) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
    • familial erythroblastic - D56.1 Beta thalassemia
    • Fanconi's (congenital pancytopenia) - D61.09 Other constitutional aplastic anemia
    • favism - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
    • fish tapeworm (D. latum) infestation - B70.0 Diphyllobothriasis
    • folate (folic acid) deficiency - D52.9 Folate deficiency anemia, unspecified
    • glucose-6-phosphate dehydrogenase (G6PD) deficiency - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
    • glutathione-reductase deficiency - D55.1 Anemia due to other disorders of glutathione metabolism
    • goat's milk - D52.0 Dietary folate deficiency anemia
    • granulocytic - See: Agranulocytosis;
    • Heinz body, congenital - D58.2 Other hemoglobinopathies
    • hemolytic - D58.9 Hereditary hemolytic anemia, unspecified
      • acquired - D59.9 Acquired hemolytic anemia, unspecified
        • autoimmune NEC - D59.1 Other autoimmune hemolytic anemias
        • infectious - D59.4 Other nonautoimmune hemolytic anemias
        • specified type NEC - D59.8 Other acquired hemolytic anemias
        • toxic - D59.4 Other nonautoimmune hemolytic anemias
        • with hemoglobinuria NEC - D59.6 Hemoglobinuria due to hemolysis from other external causes
      • acute - D59.9 Acquired hemolytic anemia, unspecified
        • due to enzyme deficiency specified type NEC - D55.8 Other anemias due to enzyme disorders
        • Lederer's - D59.1 Other autoimmune hemolytic anemias
      • autoimmune - D59.1 Other autoimmune hemolytic anemias
        • drug-induced - D59.0 Drug-induced autoimmune hemolytic anemia
      • chronic - D58.9 Hereditary hemolytic anemia, unspecified
        • idiopathic - D59.9 Acquired hemolytic anemia, unspecified
      • cold type (secondary) (symptomatic) - D59.1 Other autoimmune hemolytic anemias
      • congenital (spherocytic) - See: Spherocytosis;
      • due to
        • cardiac conditions - D59.4 Other nonautoimmune hemolytic anemias
        • drugs (nonautoimmune) - D59.2 Drug-induced nonautoimmune hemolytic anemia
          • autoimmune - D59.0 Drug-induced autoimmune hemolytic anemia
        • enzyme disorder - D55.9 Anemia due to enzyme disorder, unspecified
          • drug-induced - D59.2 Drug-induced nonautoimmune hemolytic anemia
        • presence of shunt or other internal prosthetic device - D59.4 Other nonautoimmune hemolytic anemias
      • familial - D58.9 Hereditary hemolytic anemia, unspecified
      • hereditary - D58.9 Hereditary hemolytic anemia, unspecified
        • due to enzyme disorder - D55.9 Anemia due to enzyme disorder, unspecified
          • specified type NEC - D55.8 Other anemias due to enzyme disorders
        • specified type NEC - D58.8 Other specified hereditary hemolytic anemias
      • idiopathic (chronic) - D59.9 Acquired hemolytic anemia, unspecified
      • mechanical - D59.4 Other nonautoimmune hemolytic anemias
      • microangiopathic - D59.4 Other nonautoimmune hemolytic anemias
      • nonautoimmune - D59.4 Other nonautoimmune hemolytic anemias
        • drug-induced - D59.2 Drug-induced nonautoimmune hemolytic anemia
      • nonspherocytic
        • congenital or hereditary NEC - D55.8 Other anemias due to enzyme disorders
          • glucose-6-phosphate dehydrogenase deficiency - D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
          • pyruvate kinase deficiency - D55.2 Anemia due to disorders of glycolytic enzymes
          • type
            • I - D55.1 Anemia due to other disorders of glutathione metabolism
            • II - D55.2 Anemia due to disorders of glycolytic enzymes
        • type
          • I - D55.1 Anemia due to other disorders of glutathione metabolism
          • II - D55.2 Anemia due to disorders of glycolytic enzymes
      • secondary - D59.4 Other nonautoimmune hemolytic anemias
        • autoimmune - D59.1 Other autoimmune hemolytic anemias
      • specified (hereditary) type NEC - D58.8 Other specified hereditary hemolytic anemias
      • Stransky-Regala type - See Also: Hemoglobinopathy; - D58.8 Other specified hereditary hemolytic anemias
      • symptomatic - D59.4 Other nonautoimmune hemolytic anemias
        • autoimmune - D59.1 Other autoimmune hemolytic anemias
      • toxic - D59.4 Other nonautoimmune hemolytic anemias
      • warm type (secondary) (symptomatic) - D59.1 Other autoimmune hemolytic anemias
    • hemorrhagic (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
      • acute - D62 Acute posthemorrhagic anemia
    • Herrick's - D57.1 Sickle-cell disease without crisis
    • hexokinase deficiency - D55.2 Anemia due to disorders of glycolytic enzymes
    • hookworm - B76.9 Hookworm disease, unspecified
    • hypochromic (idiopathic) (microcytic) (normoblastic) - D50.9 Iron deficiency anemia, unspecified
      • due to blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • familial sex-linked - D64.0 Hereditary sideroblastic anemia
      • pyridoxine-responsive - D64.3 Other sideroblastic anemias
      • sideroblastic, sex-linked - D64.0 Hereditary sideroblastic anemia
    • hypoplasia, red blood cells - D61.9 Aplastic anemia, unspecified
      • congenital or familial - D61.01 Constitutional (pure) red blood cell aplasia
    • hypoplastic (idiopathic) - D61.9 Aplastic anemia, unspecified
      • congenital or familial (of childhood) - D61.01 Constitutional (pure) red blood cell aplasia
    • hypoproliferative (refractive) - D61.9 Aplastic anemia, unspecified
    • idiopathic - D64.9 Anemia, unspecified
      • aplastic - D61.3 Idiopathic aplastic anemia
      • hemolytic, chronic - D59.9 Acquired hemolytic anemia, unspecified
    • in (due to) (with)
      • chronic kidney disease - D63.1 Anemia in chronic kidney disease
      • end stage renal disease - D63.1 Anemia in chronic kidney disease
      • failure, kidney (renal) - D63.1 Anemia in chronic kidney disease
      • neoplastic disease - See Also: Neoplasm; - D63.0 Anemia in neoplastic disease
    • intertropical - See Also: Ancylostomiasis; - D63.8 Anemia in other chronic diseases classified elsewhere
    • iron deficiency - D50.9 Iron deficiency anemia, unspecified
      • secondary to blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • specified type NEC - D50.8 Other iron deficiency anemias
    • Joseph-Diamond-Blackfan (congenital hypoplastic) - D61.01 Constitutional (pure) red blood cell aplasia
    • Lederer's (hemolytic) - D59.1 Other autoimmune hemolytic anemias
    • leukoerythroblastic - D61.82 Myelophthisis
    • macrocytic - D53.9 Nutritional anemia, unspecified
      • nutritional - D52.0 Dietary folate deficiency anemia
      • tropical - D52.8 Other folate deficiency anemias
    • malarial - See Also: Malaria; - B54 Unspecified malaria
    • malignant (progressive) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • malnutrition - D53.9 Nutritional anemia, unspecified
    • marsh - See Also: Malaria; - B54 Unspecified malaria
    • Mediterranean (with other hemoglobinopathy) - D56.9 Thalassemia, unspecified
    • megaloblastic - D53.1 Other megaloblastic anemias, not elsewhere classified
      • combined B12 and folate deficiency - D53.1 Other megaloblastic anemias, not elsewhere classified
      • hereditary - D51.1 Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
      • nutritional - D52.0 Dietary folate deficiency anemia
      • orotic aciduria - D53.0 Protein deficiency anemia
      • refractory - D53.1 Other megaloblastic anemias, not elsewhere classified
      • specified type NEC - D53.1 Other megaloblastic anemias, not elsewhere classified
    • megalocytic - D53.1 Other megaloblastic anemias, not elsewhere classified
    • microcytic (hypochromic) - D50.9 Iron deficiency anemia, unspecified
      • due to blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • familial - D56.8 Other thalassemias
    • microdrepanocytosis - D57.40 Sickle-cell thalassemia without crisis
    • microelliptopoikilocytic (Rietti-Greppi- Micheli) - D56.9 Thalassemia, unspecified
    • miner's - B76.9 Hookworm disease, unspecified
    • myelodysplastic - D46.9 Myelodysplastic syndrome, unspecified
    • myelofibrosis - D75.81 Myelofibrosis
    • myelogenous - D64.89 Other specified anemias
    • myelopathic - D64.89 Other specified anemias
    • myelophthisic - D61.82 Myelophthisis
    • myeloproliferative - D47.Z9 Other specified neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue
    • newborn - P61.4 Other congenital anemias, not elsewhere classified
      • due to
        • ABO (antibodies, isoimmunization, maternal/fetal incompatibility) - P55.1 ABO isoimmunization of newborn
        • Rh (antibodies, isoimmunization, maternal/fetal incompatibility) - P55.0 Rh isoimmunization of newborn
      • following fetal blood loss - P61.3 Congenital anemia from fetal blood loss
      • posthemorrhagic (fetal) - P61.3 Congenital anemia from fetal blood loss
    • nonspherocytic hemolytic - See: Anemia, hemolytic, nonspherocytic;
    • normocytic (infectional) - D64.9 Anemia, unspecified
      • due to blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • myelophthisic - D61.82 Myelophthisis
    • nutritional (deficiency) - D53.9 Nutritional anemia, unspecified
      • megaloblastic - D52.0 Dietary folate deficiency anemia
      • with
        • poor iron absorption - D50.8 Other iron deficiency anemias
        • specified deficiency NEC - D53.8 Other specified nutritional anemias
    • of prematurity - P61.2 Anemia of prematurity
    • orotaciduric (congenital) (hereditary) - D53.0 Protein deficiency anemia
    • osteosclerotic - D64.89 Other specified anemias
    • ovalocytosis (hereditary) - See: Elliptocytosis;
    • paludal - See Also: Malaria; - B54 Unspecified malaria
    • pernicious (congenital) (malignant) (progressive) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • pleochromic - D64.89 Other specified anemias
      • of sprue - D52.8 Other folate deficiency anemias
    • posthemorrhagic (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
      • acute - D62 Acute posthemorrhagic anemia
      • newborn - P61.3 Congenital anemia from fetal blood loss
    • postoperative (postprocedural)
      • due to (acute) blood loss - D62 Acute posthemorrhagic anemia
        • chronic blood loss - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
      • specified NEC - D64.9 Anemia, unspecified
    • postpartum - O90.81 Anemia of the puerperium
    • pressure - D64.89 Other specified anemias
    • progressive - D64.9 Anemia, unspecified
      • malignant - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
      • pernicious - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • protein-deficiency - D53.0 Protein deficiency anemia
    • pseudoleukemica infantum - D64.89 Other specified anemias
    • pure red cell - D60.9 Acquired pure red cell aplasia, unspecified
      • congenital - D61.01 Constitutional (pure) red blood cell aplasia
    • pyridoxine-responsive - D64.3 Other sideroblastic anemias
    • pyruvate kinase deficiency - D55.2 Anemia due to disorders of glycolytic enzymes
    • refractory - D46.4 Refractory anemia, unspecified
      • megaloblastic - D53.1 Other megaloblastic anemias, not elsewhere classified
      • sideroblastic - D46.1 Refractory anemia with ring sideroblasts
      • sideropenic - D50.9 Iron deficiency anemia, unspecified
      • with
        • excess of blasts - D46.20 Refractory anemia with excess of blasts, unspecified
          • 1 (RAEB 1) - D46.21 Refractory anemia with excess of blasts 1
          • 2 (RAEB 2) - D46.22 Refractory anemia with excess of blasts 2
          • in transformation (RAEB T) - See: Leukemia, acute myeloblastic;
        • hemochromatosis - D46.1 Refractory anemia with ring sideroblasts
        • sideroblasts (ring) (RARS) - D46.1 Refractory anemia with ring sideroblasts
      • without ring sideroblasts, so stated - D46.0 Refractory anemia without ring sideroblasts, so stated
      • without sideroblasts without excess of blasts - D46.0 Refractory anemia without ring sideroblasts, so stated
    • Rietti-Greppi-Micheli - D56.9 Thalassemia, unspecified
    • scorbutic - D53.2 Scorbutic anemia
    • secondary to
      • blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
      • hemorrhage (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
    • semiplastic - D61.89 Other specified aplastic anemias and other bone marrow failure syndromes
    • sickle-cell - See: Disease, sickle-cell;
    • sideroblastic - D64.3 Other sideroblastic anemias
      • hereditary - D64.0 Hereditary sideroblastic anemia
      • hypochromic, sex-linked - D64.0 Hereditary sideroblastic anemia
      • pyridoxine-responsive NEC - D64.3 Other sideroblastic anemias
      • refractory - D46.1 Refractory anemia with ring sideroblasts
      • secondary (due to)
        • disease - D64.1 Secondary sideroblastic anemia due to disease
        • drugs and toxins - D64.2 Secondary sideroblastic anemia due to drugs and toxins
      • specified type NEC - D64.3 Other sideroblastic anemias
    • sideropenic (refractory) - D50.9 Iron deficiency anemia, unspecified
      • due to blood loss (chronic) - D50.0 Iron deficiency anemia secondary to blood loss (chronic)
        • acute - D62 Acute posthemorrhagic anemia
    • simple chronic - D53.9 Nutritional anemia, unspecified
    • specified type NEC - D64.89 Other specified anemias
    • spherocytic (hereditary) - See: Spherocytosis;
    • splenic - D64.89 Other specified anemias
    • splenomegalic - D64.89 Other specified anemias
    • stomatocytosis - D58.8 Other specified hereditary hemolytic anemias
    • syphilitic (acquired) (late) - A52.79 Other symptomatic late syphilis
    • target cell - D64.89 Other specified anemias
    • thalassemia - D56.9 Thalassemia, unspecified
    • thrombocytopenic - See: Thrombocytopenia;
    • toxic - D61.2 Aplastic anemia due to other external agents
    • tropical - B76.9 Hookworm disease, unspecified
      • macrocytic - D52.8 Other folate deficiency anemias
    • tuberculous - A18.89 Tuberculosis of other sites
    • vegan - D51.3 Other dietary vitamin B12 deficiency anemia
    • vitamin
      • B12 deficiency (dietary) pernicious - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
      • B6-responsive - D64.3 Other sideroblastic anemias
    • von Jaksch's - D64.89 Other specified anemias
    • with (due to) (in)
      • disorder of
        • anaerobic glycolysis - D55.2 Anemia due to disorders of glycolytic enzymes
        • pentose phosphate pathway - D55.1 Anemia due to other disorders of glutathione metabolism
      • koilonychia - D50.9 Iron deficiency anemia, unspecified
    • Witts' (achlorhydric anemia) - D50.8 Other iron deficiency anemias

Footnotes

Renal Insufficiency, Chronic: Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002)

Copper: A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.

Disease: A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown.

Epidemics: Sudden outbreaks of a disease in a country or region not previously recognized in that area, or a rapid increase in the number of new cases of a previous existing endemic disease. Epidemics can also refer to outbreaks of disease in animal or plant populations.

Favism: Hemolytic anemia due to the ingestion of fava beans or after inhalation of pollen from the Vicia fava plant by persons with glucose-6-phosphate dehydrogenase deficient erythrocytes.

Folic Acid: A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.

Folic Acid: A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.

Glutathione Reductase: Catalyzes the oxidation of GLUTATHIONE to GLUTATHIONE DISULFIDE in the presence of NADP+. Deficiency in the enzyme is associated with HEMOLYTIC ANEMIA. Formerly listed as EC 1.6.4.2.

Hemochromatosis: A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)

Hexokinase: An enzyme that catalyzes the conversion of ATP and a D-hexose to ADP and a D-hexose 6-phosphate. D-Glucose, D-mannose, D-fructose, sorbitol, and D-glucosamine can act as acceptors; ITP and dATP can act as donors. The liver isoenzyme has sometimes been called glucokinase. (From Enzyme Nomenclature, 1992) EC 2.7.1.1.

Ancylostomatoidea: A superfamily of nematode parasitic hookworms consisting of four genera: ANCYLOSTOMA; NECATOR; Bunostomum; and Uncinaria. ANCYLOSTOMA and NECATOR occur in humans and other mammals. Bunostomum is common in ruminants and Uncinaria in wolves, foxes, and dogs.

Infection: Invasion of the host organism by microorganisms that can cause pathological conditions or diseases.

Iron: A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.

Malnutrition: An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement.

Molybdenum: A metallic element with the atomic symbol Mo, atomic number 42, and atomic weight 95.95. It is an essential trace element, being a component of the enzymes xanthine oxidase, aldehyde oxidase, and nitrate reductase.

Primary Myelofibrosis: A de novo myeloproliferation arising from an abnormal stem cell. It is characterized by the replacement of bone marrow by fibrous tissue, a process that is mediated by CYTOKINES arising from the abnormal clone.

Myxedema: A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips.

Necator americanus: A common parasite of humans in the moist tropics and subtropics. These organisms attach to villi in the small intestine and suck blood causing diarrhea, anorexia, and anemia.

Infant, Newborn: An infant during the first 28 days after birth.

Pentose Phosphate Pathway: An oxidative decarboxylation process that converts GLUCOSE-6-PHOSPHATE to D-ribose-5-phosphate via 6-phosphogluconate. The pentose product is used in the biosynthesis of NUCLEIC ACIDS. The generated energy is stored in the form of NADPH. This pathway is prominent in tissues which are active in the synthesis of FATTY ACIDS and STEROIDS.

Postpartum Period: In females, the period that is shortly after giving birth (PARTURITION).

Pressure: A type of stress exerted uniformly in all directions. Its measure is the force exerted per unit area. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)

Pyruvate Kinase: ATP:pyruvate 2-O-phosphotransferase. A phosphotransferase that catalyzes reversibly the phosphorylation of pyruvate to phosphoenolpyruvate in the presence of ATP. It has four isozymes (L, R, M1, and M2). Deficiency of the enzyme results in hemolytic anemia. EC 2.7.1.40.

Radiation: Emission or propagation of acoustic waves (SOUND), ELECTROMAGNETIC ENERGY waves (such as LIGHT; RADIO WAVES; GAMMA RAYS; or X-RAYS), or a stream of subatomic particles (such as ELECTRONS; NEUTRONS; PROTONS; or ALPHA PARTICLES).

Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

Transients and Migrants: People who frequently change their place of residence.

Vitamins: Organic substances that are required in small amounts for maintenance and growth, but which cannot be manufactured by the human body.

Zinc: A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

Next Term
Anemophobia