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2-Methylbutyryl-CoA dehydrogenase deficiency / 2-Methylbutyryl-CoA / Newborn screening / Hypoglycemia / Carnitine / Health / Medicine / Rare diseases
Date: 2007-06-25 16:35:43
2-Methylbutyryl-CoA dehydrogenase deficiency
2-Methylbutyryl-CoA
Newborn screening
Hypoglycemia
Carnitine
Health
Medicine
Rare diseases

Disease Name 2-METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY (2MBCD) (SHORT/BRANCHED CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY; 2METHYLBUTYRYLGLYCINURIA) Organic aciduria and fatty acid oxidation defect. Classification: Inher

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