inherited metabolic disorder

inherited metabolic disorder Show first 5 Terms

2-aminoadipic 2-oxoadipic aciduria 2-hydroxyglutaric aciduria 3-methylcrotonyl-CoA carboxylase deficiency adenylosuccinase lyase deficiency alkaptonuria ... Show All 48 Terms

2-aminoadipic 2-oxoadipic aciduria 2-hydroxyglutaric aciduria 3-methylcrotonyl-CoA carboxylase deficiency adenylosuccinase lyase deficiency alkaptonuria argininosuccinic aciduria beta-ketothiolase deficiency branched-chain keto acid dehydrogenase kinase deficiency Brunner Syndrome cerebral creatine deficiency syndrome cystathioninuria cystinuria dicarboxylic aminoaciduria diphthamide deficiency syndrome familial hypertryptophanemia fumarase deficiency gamma-amino butyric acid metabolism disorder gamma-glutamyl transpeptidase deficiency glutamate-cysteine ligase deficiency glutathione synthetase deficiency glycine encephalopathy Hartnup disease hawkinsinuria histidine metabolism disease HMG-CoA synthase 2 deficiency homocystinuria homocystinuria-megaloblastic anemia cblE type homocystinuria-megaloblastic anemia cblG type hydroxykynureninuria hyperhomocysteinemia hyperlysinemia hypermethioninemia hyperprolinemia leucine-sensitive hypoglycemia of infancy lysinuric protein intolerance multiple carboxylase deficiency organic acidemia ornithine translocase deficiency oxoglutarate dehydrogenase deficiency pentosuria phenylketonuria prolidase deficiency sarcosinemia serine deficiency systemic primary carnitine deficiency disease tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia tyrosinemia urea cycle disorder Show first 5 Terms