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Carnitine-acylcarnitine translocase deficiency
Results: 41

#	Item
31	Microsoft Word - FINALDisordersDetectableTable42511 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Carnitine-acylcarnitine translocase deficiency Fatty-acid metabolism disorder Carnitine Phenylketonuria Glutaric aciduria type 1 Systemic primary carnitine deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy
32	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us 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
33	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
34	PARENT FACT SHEET DISORDER Carnitine uptake defect (CUD) CAUSE CUD occurs when an enzyme, called “carnitine transporter” (CT), is either missing or not working properly. Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 20:00:05 Chemistry Dietary supplements Quaternary ammonium compounds Carnitine Systemic primary carnitine deficiency Hypoglycemia Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Medicine Health Hepatology
35	Disease Name Carnitine uptake deficiency Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:16:40 Systemic primary carnitine deficiency Dietary supplements Quaternary ammonium compounds Carnitine Fatty-acid metabolism disorder Medical genetics Cardiomyopathy Carnitine-acylcarnitine translocase Medicine Health Hepatology
36	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
37	SACHDNC Recommended Uniform Screening Panel1 Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2013-05-02 18:14:46 Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Fatty-acid metabolism disorder Glutaric aciduria type 1 Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
38	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
39	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
40	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us 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