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Malonyl-CoA decarboxylase deficiency
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#	Item
1	IMD Program List of Disorders, Covered Drugs, Supplements and Specialty Foods Add to Reading List Source URL: www.health.gov.on.ca Language: English - Date: 2016-03-07 08:48:57 Health Medicine Rare diseases Clinical medicine Malonyl-CoA decarboxylase deficiency Glutaric aciduria type 1 Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Inborn error of metabolism Hyperammonemia 2-Methylbutyryl-CoA dehydrogenase deficiency Newborn screening
2	TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD Add to Reading List Source URL: www.hrsa.gov Language: English Newborn screening Isovaleric acidemia Galactosemia Methylmalonic acidemia Propionic acidemia Malonyl-CoA decarboxylase deficiency Inborn error of metabolism Argininosuccinic aciduria Organic acidemia Health Rare diseases Medicine
3	Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings Add to Reading List Source URL: www.hrsa.gov Language: English Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Methylmalonic acidemia Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Galactosemia Malonyl-CoA decarboxylase deficiency Health Rare diseases Genetic genealogy
4	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:41 Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Health Medicine Rare diseases
5	Microsoft Word - Organic_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:47:00 Genetic genealogy Isovaleric acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acidemia Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medical genetics Health Rare diseases Medicine
6	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:01 Medical genetics Methylmalonic acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acid Malonyl-CoA decarboxylase deficiency Vitamin B12 Isovaleric acidemia Health Rare diseases Genetic genealogy
7	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:03:12 Medical genetics Organic acidemia Isovaleric acidemia Propionic acidemia Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
8	Microsoft Word - MCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 07:57:54 Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Medical genetics Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Medicine Health Rare diseases
9	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:31 Medical genetics Methylmalonic acidemia Newborn screening Organic acidemia Malonyl-CoA decarboxylase deficiency Propionic acidemia Methylmalonyl-CoA mutase deficiency Health Rare diseases Genetic genealogy
10	Newborn Screening in Canada Status Report – Page 1 of 3 – updated November 8, 2013 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screenin Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2013-11-18 10:15:10 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medical genetics Thiolase Carnitine Malonyl-CoA decarboxylase deficiency Health Rare diseases Medicine