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2-Methylbutyryl-CoA dehydrogenase deficiency
Results: 23

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21	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
22	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:38:00 Rare diseases Newborn screening Fatty-acid metabolism disorder Biotinidase deficiency Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine palmitoyltransferase I 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Health Genetic genealogy Medical genetics
23	MISSISSIPPI STATE DEPARTMENT OF HEALTH Newborn Screening Report[removed] AUTHORS AND CONTRIBUTORS Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2011-11-18 10:10:08 Rare diseases Inborn errors of carbohydrate metabolism Epidemiology Newborn screening Galactosemia Screening Phenylketonuria Galactose-1-phosphate uridylyltransferase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics

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