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Acyl-CoA
Results: 139

#	Item
111	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:06 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylcrotonyl-CoA carboxylase Propionic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
112	Microsoft Word - Haitian_Maine_Insert.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:00:32 Rare diseases Isovaleric acidemia Glutaric acidemia type 2 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Glutaric aciduria type 1 Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Propionic acidemia Health Genetic genealogy Medical genetics
113	Microsoft Word - Vermont Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2008-04-01 13:39:57 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
114	Microsoft Word - Haitian_New_Hampshire_Insert.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:10 Medical genetics Propionic acidemia Methylcrotonyl-CoA carboxylase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Methylcrotonyl-CoA Acyl CoA dehydrogenase Malonyl-CoA decarboxylase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
115	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
116	Microsoft Word - Rhode Island Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:25 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
117	Microsoft Word - Vermont_Haitian_Insert.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2008-04-01 13:43:08 Medical genetics Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Acyl-CoA dehydrogenase Health Rare diseases Genetic genealogy
118	Microsoft Word - Haitian_Rhode_Island_insert.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:30 Medical genetics Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylcrotonyl-CoA Very long-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase Acyl-CoA dehydrogenase Methylmalonic acidemia Health Rare diseases Genetic genealogy
119	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: chfs.ky.gov Language: English - Date: 2014-08-09 10:55:30 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
120	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: chfs.ky.gov Language: English - Date: 2014-08-09 10:28:56 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

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