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Organic acidemia
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#	Item
61	Parent Fact Sheet DISORDER Methylmalonic Acidemia Mutase Deficiency (MUT) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 18:18:59 Genetic genealogy Methylmalonic acidemia Vitamin B12 Acidosis Methylmalonic acid Protein Propionic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
62	(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
63	Microsoft Word - Amino_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:35:52 Medical genetics Maple syrup urine disease Glycine encephalopathy Newborn screening Phenylketonuria Amino acid Phenylalanine Organic acidemia Propionic acidemia Health Rare diseases Genetic genealogy
64	Maple Syrup Urine Disease (MSUD) What is maple syrup urine disease (MSUD)? Maple syrup urine disease (also known as MSUD) is an inherited condition that affects the way a person’s body uses certain parts of protein. A Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:44:42 Medicine Maple syrup urine disease BCKDHB Newborn screening Leucine Thiamine Organic acidemia Hypoglycemia Branched-chain alpha-keto acid dehydrogenase complex Health Rare diseases Chemistry
65	Volume 6, Issue 3 October 2011 State of Tennessee Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-10-04 10:57:09 Health sciences Pediatrics Epidemiology Newborn screening Medical specialties Amino acid Organic acidemia Maple syrup urine disease Carnitine Health Medicine Rare diseases
66	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
67	Microsoft PowerPoint - HAEBERLE - E-IMD.ppt Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-04-23 10:40:17 Genetic genealogy Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Inborn error of metabolism Organic acidemia Glutaric aciduria type 1 Urea cycle disorder Vitamin B12 Health Rare diseases Medicine
68	Microsoft PowerPoint - HAEBERLE - E-IMD.ppt Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2011-10-28 11:09:57 Genetic genealogy Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Inborn error of metabolism Organic acidemia Glutaric aciduria type 1 Urea cycle disorder Vitamin B12 Health Rare diseases Medicine
69	Neurologic considerations in propionic acidemia Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2012-01-04 11:28:49 Rare diseases Propionic acidemia Hyperammonemia Hypotonia Epilepsy Hyperglycinemia Organic acidemia Acidosis Electrocorticography Medicine Health Biology
70	Propionic acidemia consensus conference summary Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2012-01-04 11:28:53 Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Organic acidemia Newborn screening Inborn error of metabolism Hyperglycinemia Acidosis Health Rare diseases Medicine