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3-hydroxyacyl-CoA dehydrogenase
Results: 57

#	Item
31	Minnesota Department of Health[removed]VLCAD Action required Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:24 Rare diseases Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Hypoglycemia Acyl-CoA Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn error of lipid metabolism Health Medicine Chemistry
32	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 10:02:30 Hepatology Metabolism Fatty acids Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
33	Parent Fact Sheet Disorder Long Chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) Cause People with LCHADD have problems breaking down a fatty acid into energy for the body. LCHADD occurs when an enzyme called lo Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 05:28:49 Diabetes Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hypoglycemia 3-hydroxyacyl-CoA dehydrogenase 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Blood sugar Very long-chain acyl-coenzyme A dehydrogenase deficiency Glycogen storage disease type I Medicine Health Biology
34	PARENT FACT SHEET Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) CAUSE VLCAD occurs when the very long chain acyl-CoA dehydrogenase enzyme is missing or not working properly. This enzyme’s job is to break do Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 02:37:56 Very long-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine Metabolism Acyl CoA dehydrogenase Acyl-CoA ACADVL Health Chemistry Medicine
35	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:47:40 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Fatty-acid metabolism disorder 3-Methylcrotonyl-CoA carboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
36	Microsoft Word - MoD Fact Sheet 2011 Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:55 Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy
37	Arizona Department of Health Services Newborn Screening Program MSMS Pilot Project – Secondary Markers Amino Acid Disorders Analytes Add to Reading List Source URL: azdhs.gov Language: English - Date: 2013-07-03 16:56:45 Methylmalonic acidemia Newborn screening Isovaleric acidemia Methylmalonic acid Acyl CoA dehydrogenase Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Propionic acidemia
38	Newborn Screening Program Disorders Add to Reading List Source URL: health.utah.gov Language: English - Date: 2013-07-08 12:47:26 Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
39	Microsoft Word - MoD Fact Sheet 2011 Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:55 Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy
40	111 River Street, Hoboken, NJ 07030, USA[removed]FAX: [removed]COPYRIGHT TRANSFER AGREEMENT Add to Reading List Source URL: www.comparativephys.ca Language: English - Date: 2008-07-17 10:46:49 Biochemistry Coenzymes Fatty acids EC 1.1.1 Cellular respiration Thiolase Fatty acid metabolism Coenzyme A 3-hydroxyacyl-CoA dehydrogenase Chemistry Biology Metabolism

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