ACADM

#	Item
11	Disease Name MEDIUM CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY (MCADD) (ACADM DEFICIENCY; MCAD DEFICIENCY; MCADD DEFICIENCY) Fatty acid oxidation defect Classification: Genetic Information Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:44 Hepatology Metabolism Rare diseases Fatty acids Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Systemic primary carnitine deficiency Newborn screening Hypoglycemia Medicine Health Biology
12	Proceedings Vol. 66, No. of the XaLimmZ Acadm~ Add to Reading List Source URL: profiles.nlm.nih.gov Language: English - Date: 2001-02-20 17:41:32 Cell lines Nervous system Neurite Fetal bovine serum Neuron Cell culture Serum Biology Anatomy Blood
13	Microsoft Word - Parent MCAD.doc Add to Reading List Source URL: health.tn.gov Language: English - Date: 2008-05-30 09:44:30 Biology Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Hepatology ACADM Newborn screening Fatty acid metabolism Carnitine Health Medicine Rare diseases
14	Microsoft Word - Parent MCAD.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2008-05-30 09:44:30 Biology Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Hepatology ACADM Newborn screening Fatty acid metabolism Carnitine Health Medicine Rare diseases