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1 glyceric
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Glyceric acids — are sugar acids based upon glycerol.Many glyceric acids play critical roles in metabolism. Examples include: * 2 phosphoglycerate * 3 phosphoglycerate * 2,3 Diphosphoglycerate * 1,3 BisphosphoglycerateExternal links* … Wikipedia
Glyceric acid — Glyceric acid[1] IUPAC name 2,3 Dihydroxypropanoic … Wikipedia
D-Glyceric acidemia — Classification and external resources OMIM 220120 D Glyceric Acidemia (a.k.a. D Glyceric Aciduria) is an inherited disease, in the category of inborn errors of metabolism. It is caused by a mutation in the gene GLYCTK, which encodes the for the… … Wikipedia
Carboxylic acid — Structure of a carboxylic acid Carboxylate ion … Wikipedia
Iminoglycinuria — Classification and external resources Imine, a functional group found in imino acids ICD 10 E72.0 … Wikipedia
Organic acidemia — Organic acidemia, also called organic aciduria, is a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched chain amino acids, causing a buildup of acids which are usually not… … Wikipedia
Cystinuria — Classification and external resources Chemical structure of cystine formed from L cysteine (under biological conditions) ICD 10 E … Wikipedia
Maple syrup urine disease — Classification and external resources Isoleucine (pictured above), leucine, and valine are the branched chain amino acids that build up in MSUD. ICD … Wikipedia
Phenylketonuria — PKU redirects here. For other uses, see PKU (disambiguation). Phenylketonuria Classification and external resources ICD 10 E70.0 ICD 9 … Wikipedia
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
Lysinuric protein intolerance — Classification and external resources Lysine ICD 10 E … Wikipedia
