Phenylalanine metabolism inborn errors. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy2

Diseases36

Phenylketonurias 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 Smith-Lemli-Opitz Syndrome Refractive Errors Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Fabry Disease Ornithine Carbamoyltransferase Deficiency Disease Hypophosphatasia Brain Diseases, Metabolic Metal Metabolism, Inborn Errors Maple Syrup Urine Disease Fructose Metabolism, Inborn Errors Metabolic Diseases Porphyria, Erythropoietic Hyperargininemia Failure to Thrive Iron Metabolism Disorders Alkaptonuria Rare Diseases Citrullinemia Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Phenylketonuria, Maternal Pyruvate Dehydrogenase Complex Deficiency Disease Lysosomal Storage Diseases

Chemicals and Drugs35

Phenylalanine Hydroxylase Phenylalanine Phenylacetates Phenylalanine Ammonia-Lyase Phenylpyruvic Acids Amino Acids Tyrosine Homogentisate 1,2-Dioxygenase Ammonia-Lyases alpha-Galactosidase Argininosuccinic Acid Isovaleryl-CoA Dehydrogenase Methylmalonic Acid Prephenate Dehydratase Hydroxocobalamin Pentanoic Acids Methylmalonyl-CoA Mutase Oxidoreductases Acting on CH-CH Group Donors Carnitine Biopterin Glucose Leucine Glutarates Carbon Isotopes Pterins Tryptophan Amidinotransferases Glutaryl-CoA Dehydrogenase Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Amino Acids, Aromatic Fenclonine Phenylalanine-tRNA Ligase Adenylosuccinate Lyase Acyl-CoA Dehydrogenase Ornithine-Oxo-Acid Transaminase

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

Neonatal Screening Diagnostic Errors Magnetic Resonance Spectroscopy Models, Biological Gas Chromatography-Mass Spectrometry Mass Spectrometry Pedigree Chromatography, High Pressure Liquid

Phenomena and Processes13

Energy Metabolism Lipid Metabolism Mutation Kinetics Amino Acid Sequence Metabolism Base Sequence Metabolic Networks and Pathways Oxidation-Reduction Hydroxylation Phenotype Time Factors Homozygote

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Named Groups1

Infant, Newborn

Health Care2

Neonatal Screening Diagnostic Errors

Geographicals1

Australian Capital Territory

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

Phenylalanine Hydroxylase Phenylalanine Phenylketonurias Metabolism, Inborn Errors Phenylacetates Amino Acid Metabolism, Inborn Errors Phenylalanine Ammonia-Lyase 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 Energy Metabolism Hyperammonemia Lipid Metabolism Phenylpyruvic Acids Amino Acids Mutation Smith-Lemli-Opitz Syndrome Liver Molecular Sequence Data Tyrosine Homogentisate 1,2-Dioxygenase Infant, Newborn Refractive Errors Kinetics Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Amino Acid Sequence Ammonia-Lyases alpha-Galactosidase Fabry Disease Australian Capital Territory Ornithine Carbamoyltransferase Deficiency Disease Argininosuccinic Acid Isovaleryl-CoA Dehydrogenase Hypophosphatasia Methylmalonic Acid Metabolism Diagnostic Errors Brain Diseases, Metabolic Prephenate Dehydratase Base Sequence Hydroxocobalamin Pentanoic Acids Methylmalonyl-CoA Mutase Oxidoreductases Acting on CH-CH Group Donors Carnitine Biopterin Glucose Leucine Metal Metabolism, Inborn Errors Maple Syrup Urine Disease Fructose Metabolism, Inborn Errors Glutarates Carbon Isotopes Pterins Magnetic Resonance Spectroscopy Metabolic Networks and Pathways Tryptophan Amidinotransferases Metabolic Diseases Porphyria, Erythropoietic Glutaryl-CoA Dehydrogenase Models, Biological Hyperargininemia Oxidation-Reduction Failure to Thrive Iron Metabolism Disorders Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Alkaptonuria Hydroxylation Rare Diseases Amino Acids, Aromatic Citrullinemia Phenotype Time Factors Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gas Chromatography-Mass Spectrometry Mucopolysaccharidoses Mass Spectrometry Fenclonine Phenylalanine-tRNA Ligase Homozygote Adenylosuccinate Lyase Phenylketonuria, Maternal Acyl-CoA Dehydrogenase Brain Pyruvate Dehydrogenase Complex Deficiency Disease Lysosomal Storage Diseases Ornithine-Oxo-Acid Transaminase Pedigree Chromatography, High Pressure Liquid

No FAQ available that match "phenylalanine metabolism inborn errors"