Informaţii despre

Nume Disorders of sulfur-bearing amino-acid metabolism
Pagina Web apps.who.int

Vezi şi

Boli A-Z Cystathioninuria Early-Onset Epileptic Encephalopathy and Intellectual Disability Due to Grin2a Mutation Glycine N-Methyltransferase Deficiency Homocystinuria Due to Cystathionine Beta-Synthase Deficiency Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homocystinuria-Megaloblastic Anemia, Cble Complementation Type Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type Homocystinuria Without Methylmalonic Aciduria Hypermethioninemia Due to Adenosine Kinase Deficiency Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency Mercaptolactate-Cysteine Disulfiduria Methionine Adenosyltransferase I/iii Deficiency Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria, Cbld Type Methylmalonic Aciduria and Homocystinuria, Cblf Type Molybdenum Cofactor Deficiency, Complementation Group a Molybdenum Cofactor Deficiency, Complementation Group B Molybdenum Cofactor Deficiency, Complementation Group C Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency Sulfite Oxidase Deficiency, Isolated