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Acyl-CoA dehydrogenase
Results: 122

#	Item
11	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:42 Genetic genealogy Glutaric acidemia type 2 Fatty-acid metabolism disorder Glutaric aciduria type 1 Newborn screening Fatty acid metabolism Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
12	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:01 Medical genetics Methylmalonic acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acid Malonyl-CoA decarboxylase deficiency Vitamin B12 Isovaleric acidemia Health Rare diseases Genetic genealogy
13	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
14	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:53 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Acute fatty liver of pregnancy Hepatology Newborn screening Fatty acid metabolism Mitochondrial trifunctional protein Health Medicine Rare diseases
15	Microsoft Word - MCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 07:57:54 Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Medical genetics Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Medicine Health Rare diseases
16	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:31 Medical genetics Methylmalonic acidemia Newborn screening Organic acidemia Malonyl-CoA decarboxylase deficiency Propionic acidemia Methylmalonyl-CoA mutase deficiency Health Rare diseases Genetic genealogy
17	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:10 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Genetic genealogy 3-hydroxy-3-methylglutaryl-CoA lyase Newborn screening Protein families Fatty-acid metabolism disorder HMG-CoA reductase Health Rare diseases Medicine
18	DRAFT[removed]ARTICLE 2. NEWBORN AND INFANT SCREENING Section R9[removed]. Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2013-08-21 11:09:22 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Biotinidase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Health Rare diseases Genetic genealogy
19	METABOLIC/SICKLE CELL SCREENING GUIDELINES As mandated by KRS[removed], Newborn Screening tests include: Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-12-04 13:18:40 Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Galactosemia Methylmalonyl-CoA mutase deficiency Phenylketonuria Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
20	Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder Add to Reading List Source URL: www.dhss.delaware.gov Language: English - Date: 2012-07-26 14:33:28 Genetic genealogy Newborn screening Carnitine Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Methylmalonic acidemia Glutaric acidemia type 2 Acyl CoA dehydrogenase Health Rare diseases Medicine