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Isovaleric acidemia
Results: 160

#	Item
131	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
132	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
133	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
134	Vermont Newborn Screening Program Add to Reading List Source URL: www.nergg.org Language: English - Date: 2008-04-01 13:45:35 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Maple syrup urine disease Methylmalonic acid Very long-chain acyl-coenzyme A dehydrogenase deficiency Thiolase Health Rare diseases Genetic genealogy
135	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
136	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
137	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: www.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
138	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 16:38:00 Rare diseases Newborn screening Fatty-acid metabolism disorder Biotinidase deficiency Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine palmitoyltransferase I 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Health Genetic genealogy Medical genetics
139	Microsoft Word - refusal and disorders combination FINAL[removed]doc Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-01-31 08:10:27 Genetic genealogy Newborn screening Methylmalonic acidemia Fatty-acid metabolism disorder Propionic acidemia Isovaleric acidemia Carnitine palmitoyltransferase I Glutaric aciduria type 1 Malonyl-CoA Health Rare diseases Medicine
140	Appendix[removed]C 86 Inborn Errors of Metabolism Inborn errors of metabolism generally refer to gene mutations or gene deletions that alter metabolism in the body, including but not limited to: Amino Acid Disorders Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2013-02-08 13:02:17 Genetic genealogy Inborn errors of carbohydrate metabolism Hepatology Pediatrics Inborn error of metabolism Isovaleric acidemia Propionic acidemia Methylmalonic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases

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