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Amino acid metabolism disorders

2017-08-01T17:28:01+03:00[Europe/Moscow] en true Congenital disorders of amino acid metabolism, Methylmalonic acidemia, Carnosinemia, 3-Methylcrotonyl-CoA carboxylase deficiency, Fumarase deficiency, Type I tyrosinemia, Propionic acidemia, Oculocerebrorenal syndrome, Ocular albinism type 1, Iminoglycinuria, Prolidase deficiency, Urocanic aciduria, Lysinuric protein intolerance, Ornithine transcarbamylase deficiency, Glutaric aciduria type 1, Tetrahydrobiopterin deficiency, Beta-ketothiolase deficiency, Hawkinsinuria, Sarcosinemia, Alkaptonuria, Argininosuccinic aciduria, Citrullinemia, Phenylketonuria, Cystinosis, Homocystinuria, Hyperlysinemia, Hyperhomocysteinemia, Isovaleric acidemia, Ornithine translocase deficiency, Tyrosinemia type III, D-Glyceric acidemia, 2-Methylbutyryl-CoA dehydrogenase deficiency, Cystinuria, Fanconi syndrome, Maple syrup urine disease, Waardenburg syndrome, Hermansky–Pudlak syndrome, Tyrosinemia, Glutathione synthetase deficiency, Succinic semialdehyde dehydrogenase deficiency, Hypervalinemia, Inborn errors of renal tubular transport, Brunner syndrome, Saccharopinuria, Methylmalonyl-CoA mutase deficiency, Ornithine aminotransferase deficiency, Pipecolic acidemia, Ochronosis, Piebaldism, Ocular albinism, Oculocutaneous albinism, Guanidinoacetate methyltransferase deficiency, Hypertryptophanemia, Hartnup disease, Hyperammonemia, Histidinemia, Dopamine beta hydroxylase deficiency, Tyrosinemia type II, Dicarboxylic aminoaciduria flashcards Memtrick.com Amino acid metabolism disorders
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