congenital, disorders, amino, acid, metabolism, inborn, errors, amino, acid, metabolism, metabolic, disorders, which, impair, synthesis, degradation, amino, acids, general, structure, amino, acid, with, amino, group, left, carboxyl, group, right, specialtyendo. Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids Congenital disorders of amino acid metabolismThe general structure of an a amino acid with the amino group on the left and the carboxyl group on the right SpecialtyEndocrinology Contents 1 Types 2 Amino acid transport disorders 3 Amino acid storage disorders 4 References 5 External linksTypes editAlkaptonuria Aspartylglucosaminuria Branched chain keto acid dehydrogenase kinase deficiency Methylmalonic acidemia Maple syrup urine disease Homocystinuria Tyrosinemia Trimethylaminuria Hartnup disease Biotinidase deficiency Ornithine carbamoyltransferase deficiency Carbamoyl phosphate synthase I deficiency disease Citrullinemia Hyperargininemia Hyperhomocysteinemia Hypermethioninemia Hyperlysinemias Nonketotic hyperglycinemia Propionic acidemia HyperprolinemiaAmino acid transport disorders editCystinuria Dicarboxylic aminoaciduria Hartnup diseaseAmino acid storage disorders editGlutaric acidemia type 2References editExternal links edit nbsp This article about an endocrine nutritional or metabolic disease is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Congenital disorders of amino acid metabolism amp oldid 1088303511, wikipedia, wiki, book, books, library,
