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3-hydroxy-3-methylglutaryl-CoA lyase
Results: 9

#	Item
1	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2012-11-09 11:16:32 Genodermatoses Holocarboxylase synthetase deficiency Multiple carboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Biotinidase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Biotin Medical genetics Medicine Health Pediatrics
2	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:10 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Genetic genealogy 3-hydroxy-3-methylglutaryl-CoA lyase Newborn screening Protein families Fatty-acid metabolism disorder HMG-CoA reductase Health Rare diseases Medicine
3	3-Hydroxy-3-Methylglutaryl-CoA Lyase (HMG) Deficiency (metabolic condition: organic acid disorder) Also known as: • HMG-CoA lyase deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:32:42 Genetic genealogy Medical genetics HMG-CoA Rare diseases Protein families Newborn screening Fatty-acid metabolism disorder Health 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase
4	NEWBORN SCREENING FACT SHEET HMG Lyase Deficiency (3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency) If HMG lyase deficiency is not treated, what problems occur? Each child with HMG lyase deficiency will Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:58 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Newborn screening Biotin 3-hydroxy-3-methylglutaryl-CoA lyase Holocarboxylase synthetase Health Genetics Medicine
5	Microsoft Word - HMG update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-06-21 21:31:50 Genetic genealogy 3-hydroxy-3-methylglutaryl-CoA lyase Newborn screening HMG-CoA Fatty-acid metabolism disorder Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Health 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Medicine
6	Disease Name Hydroxymethylglutaric aciduria (3-OH 3-CH3 glutaric aciduria) Alternate name(s) Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 22:04:08 3-hydroxy-3-methylglutaryl-CoA lyase Rare diseases Hypoglycemia Pediatrics Glutaric aciduria type 1 Glycogen storage disease type I Health Medicine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
7	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
8	Disease Name Hydroxymethylglutaric aciduria (3-OH 3-CH3 glutaric aciduria) Alternate name(s) Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:53:26 3-hydroxy-3-methylglutaryl-CoA lyase Rare diseases Hypoglycemia Pediatrics Glutaric aciduria type 1 Glycogen storage disease type I Health Medicine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
9	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