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11 Possible Causes for 3 hydroxypyruvic, acid

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  • D-Glyceric Aciduria

    Only three diseases in which organic acids accumulate were known (primary hyperoxaluria, phenylketonuria and alcaptonuria).[] […] reductase') [3] [4] .[] Gene-Phenotype Relationships Location Phenotype Phenotype MIM number Inheritance Phenotype mapping key 9p13.2 Hyperoxaluria, primary, type II 260000 Autosomal recessive 3[]

  • 3-Phosphoglycerate Dehydrogenase Deficiency

    Amino acids were well tolerated and no adverse effects were documented.[] 5,10-Methylene-THF Dissipation Glycine H 2 O Tetrahydrofolic acid Dissipation L-Serine NAD NADH Hydroxypyruvic acid L-Alanine Glyoxylic acid L-Arginine Guanidoacetic acid[] Call in advance: Discuss with laboratory to arrange urgent analysis Storage and transport: A paired plasma amino acid sample required.[]

  • Sarcosinemia

    D disease D-2 glutaric aciduria Disorder of amino acid and organic acid metabolism Disorder of aromatic amino acid metabolism Disorder of beta and omega amino acid metabolism[] P-HYDROXYPYRUVATE BioCyc HMDB0000123 HMDB GO:0005739 GENE ONTOLOGY 1.0 SMILES CCC( O)C(O) O GO:0005737 GENE ONTOLOGY HMDB0000128 HMDB 1.0 C7H14N2O4S L-Cystathionine 222.06743[] See also inborn errors of metabolism v • d • e Metabolic pathology / Inborn error of metabolism ( E70-90 , 270-279 ) Amino acid Aromatic ( Phenylketonuria , Alkaptonuria ,[]

  • Thiamine

    If a mixture of amino acids is present in addition to glucose, ThTP accumulation is impaired, suggesting that the latter may occur in response to amino acid starvation.[] The enzyme is also capable of decarboxylating hydroxypyruvate in the presence of an ′acceptor aldehyde′.[] […] pyrophosphate, lipoic acid, NAD, FAD and coenzyme A.[]

  • Tiludronate

    Tiludronic acid (English) 1 reference Tiludronic acid (English) 1 reference TILUDRONIC ACID (English) 1 reference Tiludronic acid (English) 1 reference tiludronic acid (English[] METHYLPYRIDINE non-polymer 0 0M 3MT 3-METHYLTHIAZOLIUM ION non-polymer 0 0M 3PG 3-PHOSPHOGLYCERIC ACID non-polymer 0 0M 3PO TRIPHOSPATE non-polymer 0 0M 3PY 3-HYDROXYPYRUVIC[] Tiludronic Acid (OS: BAN) Tiludronique (acide) (OS: DCF) Tiludronate Disodium (OS: USAN) Tiludronate Sodium (OS: BANM) SR 41319B (IS: SanofiWinthrop) Brand Names Equidronate[]

  • 2-Aminoadipic 2-Oxoadipic Aciduria

    Medium-chain keto acids and derivatives Direct Parent Medium-chain keto acids and derivatives Alternative Parents Dicarboxylic acids and derivatives Alpha-keto acids and[] Hydroxypyruvic Acid / Orotidine-5'-Monophosphate / Flavin adenine dinucleotide / Pyruvaldehyde / Formaldehyde / 2-Amino-3-Ketobutyric Acid / D-Serine / Pyrophosphoric acid[] […] decarboxylase deficiency Asparagine Synthetase Deficiency Beta-Aminoisobutyric Acid, Urinary Excretion of Beta-Hydroxyisobutyryl CoA Deacylase Deficiency beta-ketothiolase[]

  • Phosphoenolpyruvate Carboxykinase Deficiency

    […] intermediates in urinary organic acid analysis.[] […] reductase [KO: K00049 ] [EC: ] 4200 ME2; malic enzyme 2 [KO: K00027 ] [EC: ] 10873 ME3; malic enzyme 3 [KO: K00029 ] [EC: ] 4199 ME1;[] […] enzyme PEPCK1, one of the enzymes needed for gluconeogenesis , the process by which organisms produce sugars (namely glucose) from non-carbohydrate precursors (such as amino acids[]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    Two patients were heterozygous for single amino acid replacements of unclear significance in the beta subunit of phosphorylase kinase (PHKB; {172490}). {2:Bruno et al. (1998[] Hydroxypyruvic acid 3-phosphate ? additional information ? - Please wait a moment until the data is sorted.[] […] the original fatty acid molecule.[]

  • Dihydropyrimidine Dehydrogenase Deficiency

    […] constitutes the first step of the pyrimidine degradation pathway in which the pyrimidine bases uracil and thymine are catabolised to beta-alanine and beta-aminoisobutyric acid[] […] acid L-2-Amino-3-oxobutanoic acid L-Alanine L-Arginine L-Cystathionine L-Cysteine L-Glutamic acid L-Methionine L-Serine Magnesium NAD NADH Orotidylic acid Oxoglutaric acid[] […] the pyrimidine degradation pathway, in which the pyrimidine bases uracil and thymine are catabolized to beta-alanine and the R-enantiomer of beta-AIB (beta-aminoisobutyric acid[]

  • Primary Hyperoxaluria

    Ethylphosphonic acid, glycolic acid, and THF were purchased from Aldrich (Milwaukee, WI). d , l -Glyceric acid was obtained from ICN (Cleveland, OH). Specimens.[] 4-hydroxy-2-oxoglutarate aldolase (HOGA1, PH type 3).[] […] reductase (GRHPR) activity; and type 3 (PH3), although being incompletely understood, is assumed to arise from deficiencies in the mitochondrial enzyme 4-hydroxy 2-oxoglutarate[]

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