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Hydroxyacyl-Coenzyme A dehydrogenase
Results: 114

#	Item
81	NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:51 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Health Rare diseases Genetic genealogy
82	OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:54 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
83	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.tn.gov Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy
84	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
85	2012 NBS Data--Final.xlsx Add to Reading List Source URL: azdhs.gov Language: English - Date: 2014-02-19 10:12:57 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
86	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
87	2009 Summary including hearing.xlsx Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:56 Medical genetics Propionic acidemia Isovaleric acidemia Methylmalonic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Multiple carboxylase deficiency Thalassemia Health Rare diseases Genetic genealogy
88	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
89	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
90	2009 Summary including hearing.xlsx Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:56 Medical genetics Propionic acidemia Isovaleric acidemia Methylmalonic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Multiple carboxylase deficiency Thalassemia Health Rare diseases Genetic genealogy