ICD-10-CM Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) References

"Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "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 - D55.29 Anemia due to other disorders of glycolytic enzymes
      • 2, 3 PG - D55.29 Anemia due to other 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 - D55.29 Anemia due to other 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 - D55.29 Anemia due to other disorders of glycolytic enzymes
      • hexokinase - D55.29 Anemia due to other 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 - D55.29 Anemia due to other disorders of glycolytic enzymes
      • phosphoglycerate kinase - D55.29 Anemia due to other disorders of glycolytic enzymes
      • PK - D55.21 Anemia due to pyruvate kinase deficiency
      • protein - D53.0 Protein deficiency anemia
      • pyruvate kinase - D55.21 Anemia due to pyruvate kinase deficiency
      • transcobalamin II - D51.2 Transcobalamin II deficiency
      • triose-phosphate isomerase - D55.29 Anemia due to other 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) - D59.19 Other autoimmune hemolytic anemia
    • 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 - D59.19 Other autoimmune hemolytic anemia
        • 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 - D59.19 Other autoimmune hemolytic anemia
      • autoimmune - D59.10 Autoimmune hemolytic anemia, unspecified
        • cold - D59.12 Cold autoimmune hemolytic anemia
        • drug-induced - D59.0 Drug-induced autoimmune hemolytic anemia
        • mixed - D59.13 Mixed type autoimmune hemolytic anemia
        • warm - D59.11 Warm autoimmune hemolytic anemia
      • chronic - D58.9 Hereditary hemolytic anemia, unspecified
        • idiopathic - D59.9 Acquired hemolytic anemia, unspecified
      • cold type (primary) (secondary) (symptomatic) - D59.12 Cold autoimmune hemolytic anemia
      • 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
      • mixed type (primary) (secondary) (symptomatic) - D59.13 Mixed type autoimmune hemolytic anemia
      • 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 - D55.21 Anemia due to pyruvate kinase deficiency
          • type
            • I - D55.1 Anemia due to other disorders of glutathione metabolism
            • II - D55.29 Anemia due to other disorders of glycolytic enzymes
        • type
          • I - D55.1 Anemia due to other disorders of glutathione metabolism
          • II - D55.29 Anemia due to other disorders of glycolytic enzymes
      • primary
        • autoimmune
          • cold type - D59.12 Cold autoimmune hemolytic anemia
          • mixed type - D59.13 Mixed type autoimmune hemolytic anemia
          • warm type - D59.11 Warm autoimmune hemolytic anemia
      • secondary - D59.4 Other nonautoimmune hemolytic anemias
        • autoimmune
          • cold type - D59.12 Cold autoimmune hemolytic anemia
          • mixed type - D59.13 Mixed type autoimmune hemolytic anemia
          • warm type - D59.11 Warm autoimmune hemolytic anemia
      • 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
          • cold type - D59.12 Cold autoimmune hemolytic anemia
          • mixed type - D59.13 Mixed type autoimmune hemolytic anemia
          • warm type - D59.11 Warm autoimmune hemolytic anemia
      • toxic - D59.4 Other nonautoimmune hemolytic anemias
      • warm type (primary) (secondary) (symptomatic) - D59.11 Warm autoimmune hemolytic anemia
    • 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 - D55.29 Anemia due to other 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) - D59.19 Other autoimmune hemolytic anemia
    • 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 - D64.89 Other specified anemias
    • 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 - D55.21 Anemia due to pyruvate kinase deficiency
    • 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 - D55.29 Anemia due to other 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

Applicable Clinical Terms Definitions

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.

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.

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

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.

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

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)

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.

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