Deficiency of hemoglobin. Medical search. Frequent questions

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Anatomy11

Erythrocytes Erythrocytes, Abnormal Heinz Bodies Liver Reticulocytes Cells, Cultured Erythrocyte Membrane Erythroblasts Erythroid Precursor Cells Fibroblasts Brain

Organisms11

Mice, Knockout Mice, Inbred C57BL Annelida Oligochaeta Vitreoscilla Mice, Transgenic Polychaeta Bivalvia Chironomidae Mice, Mutant Strains Whales

Diseases69

Anemia Vitamin A Deficiency Hemoglobinopathies Anemia, Iron-Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Hemoglobin C Disease Anemia, Sickle Cell Vitamin D Deficiency Folic Acid Deficiency Glucosephosphate Dehydrogenase Deficiency Thalassemia IgA Deficiency Thiamine Deficiency Anemia, Hypochromic Vitamin E Deficiency Ascorbic Acid Deficiency Magnesium Deficiency Hemoglobin SC Disease Immunologic Deficiency Syndromes beta-Thalassemia Protein C Deficiency Sickle Cell Trait IgG Deficiency Hemolysis Vitamin B 6 Deficiency alpha-Thalassemia Anemia, Hemolytic Pregnancy Complications, Hematologic Hemoglobinuria Riboflavin Deficiency Factor V Deficiency Polycythemia Antithrombin III Deficiency Metabolism, Inborn Errors Vitamin K Deficiency Diabetes Mellitus Factor VII Deficiency Protein Deficiency Factor XI Deficiency Diabetes Mellitus, Type 2 Disease Models, Animal Vitamin B Deficiency Factor XIII Deficiency Leukocyte-Adhesion Deficiency Syndrome Amino Acid Metabolism, Inborn Errors Body Weight Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Anemia, Hemolytic, Congenital Adrenal Hyperplasia, Congenital Choline Deficiency Cytochrome-c Oxidase Deficiency Kidney Failure, Chronic Diabetes Mellitus, Type 1 Lecithin Acyltransferase Deficiency Biotinidase Deficiency Methemoglobinemia Pallor Anemia, Macrocytic Yin Deficiency Lipid Metabolism, Inborn Errors Hypopituitarism Carbohydrate Metabolism, Inborn Errors Dwarfism, Pituitary Leukemia, Erythroblastic, Acute Purine-Pyrimidine Metabolism, Inborn Errors Growth Disorders

Chemicals and Drugs81

Hemoglobins Hemoglobin A Hemoglobins, Abnormal Fetal Hemoglobin Hemoglobin, Sickle Hemoglobin C Oxyhemoglobins Hemoglobin E Hemoglobin A, Glycosylated Hemoglobin A2 Methemoglobin Truncated Hemoglobins Carboxyhemoglobin Iron Oxygen Blood Substitutes Hemoglobin J Hemoglobin H Diphosphoglyceric Acids 2,3-Diphosphoglycerate Heme Globins Erythropoietin Ferritins Hematinics Carbon Monoxide Phytic Acid Haptoglobins Hemoglobin M Antisickling Agents alpha-Globins Myoglobin beta-Globins Hemin Iron, Dietary Zinc Blood Glucose Iron Isotopes Ferrous Compounds Hemeproteins Iodine Biological Markers Protoporphyrins Recombinant Proteins Transferrin Vitamin B 12 Macromolecular Substances Fructosamine Hemoglobin Subunits Nitric Oxide Vitamin A Folic Acid RNA, Messenger Copper Blood Proteins Receptors, Transferrin Amino Acids Phenylhydrazines Serum Albumin Hydroxyurea gamma-Globins Vitamin D Glucosephosphate Dehydrogenase Ferric Compounds Sulfhemoglobin Histidine Hypoglycemic Agents Erythrocruorins Mercuribenzoates Selenium alpha 1-Antitrypsin Human Growth Hormone Micronutrients Fatty Acids, Essential Bilirubin Leghemoglobin Steroid 21-Hydroxylase Methylmalonic Acid Porphyrins Chromium Isotopes Iron Compounds

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

Hemoglobinometry Hematocrit Erythrocyte Indices Erythrocyte Count Blood Protein Electrophoresis Electrophoresis, Cellulose Acetate Spectrophotometry Reticulocyte Count Hematologic Tests Exchange Transfusion, Whole Blood Pedigree Blood Transfusion Electrophoresis, Starch Gel Isoelectric Focusing Disease Models, Animal Blood Cell Count Chromatography, High Pressure Liquid Reference Values Spectroscopy, Near-Infrared Body Weight Risk Factors Renal Dialysis Prevalence Erythrocyte Transfusion Prospective Studies Treatment Outcome Blood Chemical Analysis Retrospective Studies Osmotic Fragility Hemodilution Cross-Sectional Studies Bloodletting Oximetry Spectrum Analysis Chromatography, Ion Exchange Models, Biological Spectrum Analysis, Raman Follow-Up Studies Cohort Studies Polymerase Chain Reaction Case-Control Studies Analysis of Variance

Phenomena and Processes42

Hematocrit Erythrocyte Indices Erythrocyte Count Mutation Hemolysis Erythropoiesis Hydrogen-Ion Concentration Heterozygote Kinetics Time Factors Homozygote Phenotype Reticulocyte Count Pregnancy Amino Acid Sequence Nutritional Status Protein Binding Blood Cell Count Oxidation-Reduction Base Sequence Diet Protein Conformation Body Weight Erythrocyte Volume Erythrocyte Aging Photolysis Allosteric Regulation Partial Pressure Genotype Osmotic Fragility Oxygen Consumption Point Mutation Binding Sites Dose-Response Relationship, Drug Altitude Gene Expression Regulation Consanguinity Gene Deletion Temperature Alleles Erythrocyte Deformability Oxidative Stress

Technology, Industry, Agriculture4

Blood Substitutes Dietary Supplements Food, Fortified Micronutrients

Information Science4

Molecular Sequence Data Amino Acid Sequence Base Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care14

Nutritional Status Risk Factors Prevalence Prospective Studies Treatment Outcome Retrospective Studies Cross-Sectional Studies Follow-Up Studies Cohort Studies Altitude Age Factors Temperature Case-Control Studies Analysis of Variance

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Technology, Industry, Agriculture Information Science Named Groups Health Care

Hemoglobins Hemoglobin A Hemoglobins, Abnormal Fetal Hemoglobin Hemoglobin, Sickle Hemoglobin C Oxyhemoglobins Hemoglobin E Hemoglobin A, Glycosylated Hemoglobin A2 Methemoglobin Anemia Truncated Hemoglobins Vitamin A Deficiency Hemoglobinopathies Hemoglobinometry Carboxyhemoglobin Anemia, Iron-Deficiency Deficiency Diseases Iron Erythrocytes Oxygen alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Hemoglobin C Disease Blood Substitutes Hemoglobin J Hemoglobin H Anemia, Sickle Cell Diphosphoglyceric Acids Vitamin D Deficiency Hematocrit Folic Acid Deficiency Glucosephosphate Dehydrogenase Deficiency 2,3-Diphosphoglycerate Thalassemia Heme IgA Deficiency Thiamine Deficiency Globins Anemia, Hypochromic Erythropoietin Erythrocyte Indices Ferritins Erythrocyte Count Hematinics Vitamin E Deficiency Ascorbic Acid Deficiency Magnesium Deficiency Mice, Knockout Carbon Monoxide Hemoglobin SC Disease Phytic Acid Blood Protein Electrophoresis Haptoglobins Immunologic Deficiency Syndromes beta-Thalassemia Protein C Deficiency Sickle Cell Trait Mutation IgG Deficiency Hemolysis Vitamin B 6 Deficiency Erythrocytes, Abnormal alpha-Thalassemia Hemoglobin M Anemia, Hemolytic Erythropoiesis Antisickling Agents Pregnancy Complications, Hematologic Hydrogen-Ion Concentration alpha-Globins Hemoglobinuria Myoglobin Riboflavin Deficiency Factor V Deficiency Mice, Inbred C57BL Heterozygote Kinetics beta-Globins Polycythemia Time Factors Hemin Homozygote Molecular Sequence Data Iron, Dietary Electrophoresis, Cellulose Acetate Spectrophotometry Zinc Phenotype Antithrombin III Deficiency Reticulocyte Count Hematologic Tests Blood Glucose Heinz Bodies Metabolism, Inborn Errors Liver Exchange Transfusion, Whole Blood Pregnancy Vitamin K Deficiency

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