Hemochromatosis iron overload. Medical search. Frequent questions

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Anatomy6

Liver Mononuclear Phagocyte System Duodenum Myocardium Chromosomes, Human, Pair 6 Hepatocytes

Organisms2

Mice, Knockout Mice, Inbred C57BL

Diseases23

Hemochromatosis Iron Overload beta-Thalassemia Hemosiderosis Iron Metabolism Disorders Siderosis Thalassemia Porphyria Cutanea Tarda Anemia, Iron-Deficiency Anemia, Sideroblastic Liver Diseases Liver Cirrhosis Anemia, Hypochromic Metal Metabolism, Inborn Errors Anemia, Dyserythropoietic, Congenital Anemia Disease Models, Animal Liver Diseases, Alcoholic Fatty Liver Cardiomegaly Anemia, Sickle Cell Anemia, Hemolytic, Congenital Nonspherocytic Myelodysplastic Syndromes

Chemicals and Drugs36

Iron Iron Chelating Agents Ferritins Hepcidins Transferrin Histocompatibility Antigens Class I Antimicrobial Cationic Peptides Deferoxamine Receptors, Transferrin Membrane Proteins Iron, Dietary HLA Antigens Cation Transport Proteins Iron-Dextran Complex Iron Radioisotopes Hemosiderin Iron Compounds Pyridones Iron Carbonyl Compounds Iron-Binding Proteins Ferric Compounds Apoferritins Benzoates Iron-Regulatory Proteins Ferrous Compounds Iron Isotopes Siderophores GPI-Linked Proteins Bone Morphogenetic Protein 6 beta 2-Microglobulin Ceruloplasmin Hemoglobins Uroporphyrinogen Decarboxylase Triazoles HLA-A Antigens Iron Regulatory Protein 1

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Phlebotomy Chelation Therapy Blood Transfusion Bloodletting Genetic Testing Erythrocyte Transfusion Cytapheresis Disease Models, Animal Amino Acid Substitution Biopsy Pedigree Erythrocyte Indices Magnetic Resonance Imaging DNA Mutational Analysis

Phenomena and Processes17

Homozygote Mutation Genotype Heterozygote Homeostasis Mutation, Missense Intestinal Absorption Penetrance Point Mutation Phenotype Erythropoiesis Amino Acid Substitution Chromosomes, Human, Pair 6 Gene Frequency Erythrocyte Indices Alleles Gene Expression Regulation

Humanities1

Health Care2

Genetic Testing Family Health

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Humanities Health Care

Hemochromatosis Iron Overload Iron Iron Chelating Agents Ferritins Hepcidins Transferrin Phlebotomy Chelation Therapy Histocompatibility Antigens Class I Antimicrobial Cationic Peptides beta-Thalassemia Hemosiderosis Deferoxamine Receptors, Transferrin Iron Metabolism Disorders Membrane Proteins Iron, Dietary Siderosis HLA Antigens Cation Transport Proteins Homozygote Iron-Dextran Complex Liver Thalassemia Blood Transfusion Porphyria Cutanea Tarda Iron Radioisotopes Hemosiderin Iron Compounds Pyridones Iron Carbonyl Compounds Bloodletting Iron-Binding Proteins Anemia, Iron-Deficiency Mutation Ferric Compounds Anemia, Sideroblastic Apoferritins Liver Diseases Benzoates Genotype Liver Cirrhosis Heterozygote Genetic Testing Iron-Regulatory Proteins Homeostasis Ferrous Compounds Iron Isotopes Mononuclear Phagocyte System Anemia, Hypochromic Mutation, Missense Metal Metabolism, Inborn Errors Duodenum Siderophores Intestinal Absorption Erythrocyte Transfusion GPI-Linked Proteins Bone Morphogenetic Protein 6 Penetrance beta 2-Microglobulin Ceruloplasmin Anemia, Dyserythropoietic, Congenital Point Mutation Hemoglobins Anemia Mythology Phenotype Erythropoiesis Cytapheresis Disease Models, Animal Uroporphyrinogen Decarboxylase Triazoles Amino Acid Substitution Biopsy Myocardium Mice, Knockout Mice, Inbred C57BL Chromosomes, Human, Pair 6 Liver Diseases, Alcoholic Gene Frequency HLA-A Antigens Pedigree Erythrocyte Indices Fatty Liver Hepatocytes Family Health Cardiomegaly Anemia, Sickle Cell Magnetic Resonance Imaging DNA Mutational Analysis Alleles Iron Regulatory Protein 1 Gene Expression Regulation Anemia, Hemolytic, Congenital Nonspherocytic Myelodysplastic Syndromes

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