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2-Methylbutyryl-CoA
Results: 23

#	Item
1	IMD Program List of Disorders, Covered Drugs, Supplements and Specialty Foods Add to Reading List Source URL: www.health.gov.on.ca Language: English - Date: 2016-03-07 08:48:57 Health Medicine Rare diseases Clinical medicine Malonyl-CoA decarboxylase deficiency Glutaric aciduria type 1 Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Inborn error of metabolism Hyperammonemia 2-Methylbutyryl-CoA dehydrogenase deficiency Newborn screening
2	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:18 Medical genetics Newborn screening Organic acidemia 2-Methylbutyryl-CoA dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
3	Title 15 - Mississippi Department of Health Add to Reading List Source URL: www.msdh.state.ms.us Language: English - Date: 2014-03-27 09:48:48 Newborn screening Congenital adrenal hyperplasia Galactosemia Phenylketonuria Biotinidase deficiency Congenital hypothyroidism 3-Methylcrotonyl-CoA carboxylase deficiency Inborn error of metabolism 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
4	Microsoft Word - 2MBCD_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-11-28 02:11:01 Epidemiology Newborn screening Pediatrics 2-Methylbutyryl-CoA dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Health Genetic genealogy Medical genetics
5	NEWBORN SCREENING FACT SHEET 2MBDH Deficiency (2-Methylbutyryl CoA Dehydrogenase Deficiency) What is it? 2MBDH deficiency is one type of organic acid disorder. People with 2MBDH deficiency have Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:54 Rare diseases Pediatrics Epidemiology Newborn screening Biotinidase deficiency Copper in health Health Medicine Genetic genealogy
6	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 Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:43 2-Methylbutyryl-CoA dehydrogenase deficiency 2-Methylbutyryl-CoA Newborn screening Hypoglycemia Carnitine Health Medicine Rare diseases
7	Title 15 - Mississippi Department of Health Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2014-03-27 09:48:48 Newborn screening Congenital adrenal hyperplasia Galactosemia Phenylketonuria Biotinidase deficiency Congenital hypothyroidism 3-Methylcrotonyl-CoA carboxylase deficiency Inborn error of metabolism 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
8	Microsoft Word - 2mbcd_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:45 Coenzymes 2-Methylbutyryl-CoA dehydrogenase deficiency Rare diseases ACADSB ACADS Butyryl-CoA dehydrogenase Acyl-CoA Newborn screening 2-Methylbutyryl-CoA Biology Chemistry Health
9	Minnesota Department of Health[removed]SBCAD Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:23 Epidemiology Newborn screening Pediatrics 2-Methylbutyryl-CoA dehydrogenase deficiency Carnitine 2-Methylbutyryl-CoA Hypoglycemia Heparin Health Medicine Chemistry
10	2012 POSITIVE NEWBORN SCREEN FAMILY FACT SHEET Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:14 Medical tests Epidemiology Newborn screening Screening 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics