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Nume Other disorders of branched-chain amino-acid metabolism
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Boli A-Z 2-Methylbutyryl-Coa Dehydrogenase Deficiency 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 3-Hydroxyisobutyric Aciduria 3-Hydroxyisobutyryl-Coa Hydrolase Deficiency 3-Methylcrotonyl-Coa Carboxylase Deficiency 3-Methylglutaconic Aciduria 3-Methylglutaconic Aciduria, Type I 3-Methylglutaconic Aciduria, Type Iii 3-Methylglutaconic Aciduria, Type Iv 3-Methylglutaconic Aciduria, Type V 3-Methylglutaconic Aciduria with Cataracts, Neurologic Involvement, and Neutropenia 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome Alpha-Methylacetoacetic Aciduria Barth Syndrome Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency Combined Malonic and Methylmalonic Aciduria Isobutyryl-Coa Dehydrogenase Deficiency Isovaleric Acidemia Methylmalonate Semialdehyde Dehydrogenase Deficiency Methylmalonic Acidemia and Homocysteinemia, Cblx Type Methylmalonic Acidemia Cb1a Type Methylmalonic Acidemia Cb1b Type Methylmalonic Acidemia Due to Transcobalamin Receptor Defect Methylmalonic Acidemia with Homocystinuria Methylmalonic Aciduria and Homocystinuria, Cbld Type Methylmalonic Aciduria and Homocystinuria, Cblj Type Methylmalonic Aciduria, Cbla Type Methylmalonic Aciduria, Cblb Type Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect Methylmalonyl-Coa Epimerase Deficiency Mitochondrial Dna Depletion Syndrome 9 Propionic Acidemia Vitamin B12-Responsive Methylmalonic Acidemia