Genetics of hereditary hemochromatosis. Medical search. Frequent questions

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Anatomy4

Liver Duodenum Chromosomes, Human, Pair 6 Hepatocytes

Organisms1

Diseases10

Hemochromatosis Iron Overload Iron Metabolism Disorders Porphyria Cutanea Tarda Liver Cirrhosis Anemia, Iron-Deficiency Liver Diseases Genetic Predisposition to Disease Hemosiderosis Carcinoma, Hepatocellular

Chemicals and Drugs16

Histocompatibility Antigens Class I Iron Transferrin Hepcidins Receptors, Transferrin Membrane Proteins HLA Antigens Ferritins Antimicrobial Cationic Peptides Cation Transport Proteins Iron Radioisotopes Iron-Binding Proteins Iron Chelating Agents beta 2-Microglobulin Iron, Dietary Aspartate Aminotransferases

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Phlebotomy Genetic Testing Chelation Therapy Amino Acid Substitution Polymerase Chain Reaction

Phenomena and Processes15

Homozygote Mutation Penetrance Chromosomes, Human, Pair 6 Genotype Heterozygote Mutation, Missense Homeostasis Phenotype Intestinal Absorption Point Mutation Gene Frequency Alleles Amino Acid Substitution Genetic Predisposition to Disease

Disciplines and Occupations2

Genetics Genetics, Population

Health Care1

Genetic Testing

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

Hemochromatosis Iron Overload Phlebotomy Histocompatibility Antigens Class I Iron Transferrin Hepcidins Receptors, Transferrin Membrane Proteins HLA Antigens Ferritins Antimicrobial Cationic Peptides Iron Metabolism Disorders Homozygote Cation Transport Proteins Porphyria Cutanea Tarda Iron Radioisotopes Mutation Iron-Binding Proteins Liver Iron Chelating Agents Genetic Testing Duodenum Penetrance Chromosomes, Human, Pair 6 Genotype beta 2-Microglobulin Genetics Heterozygote Iron, Dietary Mutation, Missense Liver Cirrhosis Homeostasis Anemia, Iron-Deficiency Phenotype Chelation Therapy Intestinal Absorption Point Mutation Liver Diseases Gene Frequency Alleles Amino Acid Substitution Genetic Predisposition to Disease Hemosiderosis Aspartate Aminotransferases Hepatocytes Mice, Knockout Polymerase Chain Reaction Carcinoma, Hepatocellular Genetics, Population

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