Metals metal metabolism inborn errors. Medical search. Frequent questions

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Anatomy6

Liver Brain Fibroblasts Microsomes, Liver Cells, Cultured Erythrocytes

Organisms2

Escherichia coli Mice, Knockout

Diseases44

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 Iron Metabolism Disorders Porphyria, Erythropoietic 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 Disease Models, Animal

Chemicals and Drugs86

Metals Copper Metallothionein Zinc Metals, Alkali Cobalt Homogentisate 1,2-Dioxygenase alpha-Galactosidase Nickel Argininosuccinic Acid Metals, Alkaline Earth Manganese Isovaleryl-CoA Dehydrogenase Methylmalonic Acid Oxidoreductases Acting on CH-CH Group Donors Hydroxocobalamin Pentanoic Acids Methylmalonyl-CoA Mutase Carnitine Cations, Divalent Glutarates Iron Glucose Amidinotransferases Glutaryl-CoA Dehydrogenase Chromium Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Lead Chelating Agents Adenylosuccinate Lyase Acyl-CoA Dehydrogenase Oxidoreductases Mercury Ornithine-Oxo-Acid Transaminase Soil Pollutants Fatty Acids Ions Magnesium Metals, Rare Earth Argininosuccinate Lyase Ammonia Coordination Complexes Metal Ceramic Alloys Uroporphyrinogen III Synthetase Urea Cytochrome P-450 Enzyme System Ornithine Metalloproteins Carbon Cholesterol Phenylalanine Hydroxylase Water Pollutants, Chemical DNA Amino Acids Acyl-CoA Dehydrogenases Bile Acids and Salts Vitamin B 12 Trace Elements Bacterial Proteins Metals, Light Cations Dental Alloys Chromium Alloys Arsenic Aluminum Edetic Acid Oxygen Carbon Isotopes Acetates Carbon Radioisotopes Lactic Acid Nitrogen Insulin Arginine RNA, Messenger Titanium Calcium Stainless Steel DNA Primers Organometallic Compounds Adenosine Triphosphate Alloys Lactates Phenanthrolines Gallium Environmental Pollutants

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

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

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes34

Energy Metabolism Lipid Metabolism Mutation Metabolism Kinetics Metabolic Networks and Pathways Oxidation-Reduction Amino Acid Sequence Base Sequence Time Factors Phenotype Binding Sites Biotransformation Homozygote Hydrogen-Ion Concentration Glycolysis Diet, Protein-Restricted Consanguinity Catalysis Algorithms Mutation, Missense Protein Binding Oxygen Consumption Substrate Specificity Genotype Biological Transport Molecular Structure Homeostasis Heterozygote Alleles Temperature Pregnancy Dose-Response Relationship, Drug Protein Conformation

Technology, Industry, Agriculture8

Metal Ceramic Alloys Trace Elements Dental Alloys Chromium Alloys Welding Metallurgy Stainless Steel Alloys

Information Science5

Molecular Sequence Data Amino Acid Sequence Base Sequence Algorithms Computer Simulation

Named Groups1

Infant, Newborn

Health Care8

Neonatal Screening Diagnostic Errors Reproducibility of Results Critical Pathways Technology Assessment, Biomedical Environmental Monitoring Temperature 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 Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Metabolism, Inborn Errors Metals Metal Metabolism, Inborn Errors Copper Metallothionein 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 Zinc Smith-Lemli-Opitz Syndrome Metals, Alkali Cobalt Infant, Newborn Refractive Errors Homogentisate 1,2-Dioxygenase Mutation Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors alpha-Galactosidase Liver Molecular Sequence Data Fabry Disease Nickel Australian Capital Territory Ornithine Carbamoyltransferase Deficiency Disease Argininosuccinic Acid Metals, Alkaline Earth Manganese Isovaleryl-CoA Dehydrogenase Hypophosphatasia Brain Diseases, Metabolic Methylmalonic Acid Diagnostic Errors Oxidoreductases Acting on CH-CH Group Donors Hydroxocobalamin Pentanoic Acids Methylmalonyl-CoA Mutase Carnitine Metabolism Cations, Divalent Fructose Metabolism, Inborn Errors Magnetic Resonance Spectroscopy Kinetics Glutarates Iron Maple Syrup Urine Disease Glucose Amidinotransferases Metabolic Diseases Iron Metabolism Disorders Porphyria, Erythropoietic Glutaryl-CoA Dehydrogenase Metabolic Networks and Pathways Chromium Oxidation-Reduction Hyperargininemia Amino Acid Sequence Failure to Thrive Base Sequence Models, Biological Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Alkaptonuria Rare Diseases Time Factors Citrullinemia Mass Spectrometry Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Lead Chelating Agents Adenylosuccinate Lyase Acyl-CoA Dehydrogenase Pyruvate Dehydrogenase Complex Deficiency Disease Oxidoreductases Mercury Lysosomal Storage Diseases Ornithine-Oxo-Acid Transaminase Soil Pollutants Phenotype Neuroaxonal Dystrophies Hyperoxaluria, Primary Fatty Acids Genetic Diseases, Inborn Brain Ions Binding Sites Biotransformation Magnesium Homozygote

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