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Organic acidemia
Results: 73

#	Item
51	Organic Acid Disorders Information for Parents  Overview Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:36 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Organic acidemia Beta-ketothiolase deficiency Multiple carboxylase deficiency Health Rare diseases Genetic genealogy
52	Parent Fact Sheet DISORDER Hydroxymethylglutaric Aciduria (3-OH 3 CH3 glutaric aciduria) (HMG) CAUSE Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 17:32:51 Medical genetics Coenzymes Thioesters HMG-CoA Organic acidemia 3-hydroxy-3-methylglutaryl-CoA lyase Fatty-acid metabolism disorder 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Health Genetic genealogy
53	PARENT FACT SHEET DISORDER Glutaric acidemia, type 1 (GA-1) CAUSE GA-1 occurs when an enzyme called “glutaryl-CoA dehydrogenase” is either missing or not working properly. Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 13:47:23 Proteinogenic amino acids Organic chemistry Health Glutaric aciduria type 1 Nutrition Nitrogen metabolism Lysine Protein Tryptophan Chemistry Essential amino acids Ketogenic amino acids
54	Disease Name Glutaric acidemia, type 1 Alternate name(s) Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 08:58:53 Health Medicine Glutaryl-CoA dehydrogenase Glutaryl-CoA Carnitine Lysine Riboflavin Organic acidemia Cerebral palsy Chemistry Coenzymes Glutaric aciduria type 1
55	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: www.chfs.ky.gov Language: English - Date: 2014-09-09 03:31:10 Genetic genealogy Methylmalonic acidemia Vitamin B12 Acidosis Methylmalonic acid Protein Propionic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
56	Parent Fact Sheet Disorder Propionic Acidemia (PA) Cause Propionic Acidemia (PA) is one type of organic acid disorder. People with PA have problems breaking down and using certain amino acids from the foods they eat. PA Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 11:33:50 Genetic genealogy Propionic acidemia Carnitine Acidosis Maple syrup urine disease Methylmalonic acidemia Health Rare diseases Medicine
57	PARENT FACT SHEET DISORDER Glutaric acidemia, type 1 (GA-1) CAUSE GA-1 occurs when an enzyme called “glutaryl-CoA dehydrogenase” is either missing or not working properly. Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 10:38:55 Proteinogenic amino acids Organic chemistry Health Glutaric aciduria type 1 Nutrition Nitrogen metabolism Lysine Protein Tryptophan Chemistry Essential amino acids Ketogenic amino acids
58	Parent Fact Sheet DISORDER Methylmalonic Acidemia (Cbl A, B) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have problems Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 13:38:50 Genetic genealogy Vitamin B12 Methylmalonic acidemia Methylmalonic acid Acidosis Protein Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
59	Disease Name Glutaric acidemia, type 1 Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 18:36:55 Health Medicine Glutaryl-CoA dehydrogenase Glutaryl-CoA Carnitine Lysine Riboflavin Organic acidemia Cerebral palsy Chemistry Coenzymes Glutaric aciduria type 1
60	Parent Fact Sheet DISORDER Hydroxymethylglutaric Aciduria (3-OH 3 CH3 glutaric aciduria) (HMG) CAUSE Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 02:11:05 Medical genetics Coenzymes Thioesters HMG-CoA Organic acidemia 3-hydroxy-3-methylglutaryl-CoA lyase Fatty-acid metabolism disorder 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Health Genetic genealogy