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3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Results: 111

#	Item
1	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2015-01-29 18:14:10 Newborn screening Isovaleric acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Biotinidase deficiency Galactosemia Methylmalonic acid Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Guthrie test Health Rare diseases Medicine
2	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial Add to Reading List Source URL: azdhs.gov Language: English - Date: 2015-01-29 18:14:10 Newborn screening Isovaleric acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Biotinidase deficiency Galactosemia Methylmalonic acid Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Guthrie test Health Rare diseases Medicine
3	Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2015-02-26 15:37:45 Rare diseases Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Carnitine Biotinidase deficiency Biotin Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
4	Disorders and Reference Ranges Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
5	Disorders and Reference Ranges Add to Reading List Source URL: azdhs.gov Language: English - Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
6	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.state.tn.us 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
7	Microsoft Word - VLCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 09:09:50 Medical genetics Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
8	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
9	Microsoft Word - FAOD.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:47:24 Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein deficiency Newborn screening Lipid Health Medicine Rare diseases
10	Microsoft Word - Canada NBS status Nov23.2006.doc Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:32 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Hyperammonemia Glutaric aciduria type 1 Thiolase Methylmalonyl-CoA mutase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine

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