Body metal metabolism inborn errors. Medical search. Frequent questions

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Anatomy6

Liver Brain Fibroblasts Microsomes, Liver Cells, Cultured Erythrocytes

Organisms1

Diseases43

Metabolism, Inborn Errors Metal Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Carbohydrate Metabolism, Inborn Errors Urea Cycle Disorders, Inborn Brain Diseases, Metabolic, Inborn Argininosuccinic Aciduria Hyperammonemia Phenylketonurias Smith-Lemli-Opitz Syndrome Refractive Errors Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Fabry Disease Ornithine Carbamoyltransferase Deficiency Disease Hypophosphatasia Brain Diseases, Metabolic Fructose Metabolism, Inborn Errors Maple Syrup Urine Disease Metabolic Diseases Porphyria, Erythropoietic Iron Metabolism Disorders Hyperargininemia Failure to Thrive Alkaptonuria Rare Diseases Citrullinemia Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Pyruvate Dehydrogenase Complex Deficiency Disease Lysosomal Storage Diseases Neuroaxonal Dystrophies Hyperoxaluria, Primary Genetic Diseases, Inborn Renal Tubular Transport, Inborn Errors Intellectual Disability Nervous System Diseases Liver Diseases Immunologic Deficiency Syndromes

Chemicals and Drugs60

Metals Metallothionein Copper Homogentisate 1,2-Dioxygenase alpha-Galactosidase Argininosuccinic Acid Isovaleryl-CoA Dehydrogenase Methylmalonic Acid Hydroxocobalamin Pentanoic Acids Oxidoreductases Acting on CH-CH Group Donors Methylmalonyl-CoA Mutase Carnitine Glutarates Amidinotransferases Glucose Glutaryl-CoA Dehydrogenase Zinc Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Cobalt Metals, Alkali Adenylosuccinate Lyase Acyl-CoA Dehydrogenase Ornithine-Oxo-Acid Transaminase Fatty Acids Oxidoreductases Nickel Argininosuccinate Lyase Manganese Iron Uroporphyrinogen III Synthetase Ammonia Metals, Alkaline Earth Ornithine Cytochrome P-450 Enzyme System Urea Cholesterol Phenylalanine Hydroxylase Cations, Divalent Acyl-CoA Dehydrogenases Bile Acids and Salts Vitamin B 12 Chromium Carbon Amino Acids DNA Carbon Isotopes Carbon Radioisotopes Lactic Acid Insulin Lead Acetates Arginine Chelating Agents Nitrogen Mercury Lactates Oxygen Soil Pollutants Magnesium

Analytical, Diagnostic and Therapeutic Techniques and Equipment18

Neonatal Screening Diagnostic Errors Magnetic Resonance Spectroscopy Models, Biological Mass Spectrometry Pedigree Gas Chromatography-Mass Spectrometry Tandem Mass Spectrometry Reference Values Reproducibility of Results Phlebotomy Blood Specimen Collection Diet, Protein-Restricted Chromatography, High Pressure Liquid DNA Mutational Analysis Polymerase Chain Reaction Gene Expression Profiling Genetic Testing

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes26

Energy Metabolism Lipid Metabolism Mutation Metabolism Metabolic Networks and Pathways Base Sequence Kinetics Time Factors Oxidation-Reduction Amino Acid Sequence Phenotype Homozygote Biotransformation Diet, Protein-Restricted Glycolysis Consanguinity Algorithms Mutation, Missense Genotype Oxygen Consumption Heterozygote Hydrogen-Ion Concentration Alleles Binding Sites Biological Transport Pregnancy

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Algorithms Computer Simulation

Named Groups1

Infant, Newborn

Health Care6

Neonatal Screening Diagnostic Errors Reproducibility of Results Critical Pathways Technology Assessment, Biomedical Genetic Testing

Geographicals1

Australian Capital Territory

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care Geographicals

Metabolism, Inborn Errors Metal Metabolism, Inborn Errors Metals Metallothionein Copper Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Neonatal Screening Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Carbohydrate Metabolism, Inborn Errors Urea Cycle Disorders, Inborn Brain Diseases, Metabolic, Inborn Argininosuccinic Aciduria Hyperammonemia Energy Metabolism Lipid Metabolism Phenylketonurias Smith-Lemli-Opitz Syndrome Infant, Newborn Refractive Errors Homogentisate 1,2-Dioxygenase Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors alpha-Galactosidase Mutation Fabry Disease Liver Australian Capital Territory Ornithine Carbamoyltransferase Deficiency Disease Argininosuccinic Acid Isovaleryl-CoA Dehydrogenase Hypophosphatasia Methylmalonic Acid Brain Diseases, Metabolic Diagnostic Errors Hydroxocobalamin Pentanoic Acids Oxidoreductases Acting on CH-CH Group Donors Methylmalonyl-CoA Mutase Carnitine Molecular Sequence Data Metabolism Fructose Metabolism, Inborn Errors Glutarates Maple Syrup Urine Disease Amidinotransferases Glucose Metabolic Diseases Porphyria, Erythropoietic Glutaryl-CoA Dehydrogenase Zinc Iron Metabolism Disorders Hyperargininemia Metabolic Networks and Pathways Failure to Thrive Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Magnetic Resonance Spectroscopy Alkaptonuria Rare Diseases Citrullinemia Models, Biological Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Base Sequence Kinetics Cobalt Metals, Alkali Adenylosuccinate Lyase Acyl-CoA Dehydrogenase Time Factors Mass Spectrometry Oxidation-Reduction Pyruvate Dehydrogenase Complex Deficiency Disease Lysosomal Storage Diseases Ornithine-Oxo-Acid Transaminase Neuroaxonal Dystrophies Amino Acid Sequence Hyperoxaluria, Primary Phenotype Fatty Acids Genetic Diseases, Inborn Oxidoreductases Homozygote Brain Pedigree Biotransformation Renal Tubular Transport, Inborn Errors Gas Chromatography-Mass Spectrometry Nickel Fibroblasts Argininosuccinate Lyase Tandem Mass Spectrometry Manganese Iron Uroporphyrinogen III Synthetase Ammonia Metals, Alkaline Earth Ornithine

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