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Propionic acidemia
Results: 173

#	Item
141	Microsoft Word - refusal and disorders combination FINAL[removed]doc Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-01-31 08:10:27 Genetic genealogy Newborn screening Methylmalonic acidemia Fatty-acid metabolism disorder Propionic acidemia Isovaleric acidemia Carnitine palmitoyltransferase I Glutaric aciduria type 1 Malonyl-CoA Health Rare diseases Medicine
142	Appendix[removed]C 86 Inborn Errors of Metabolism Inborn errors of metabolism generally refer to gene mutations or gene deletions that alter metabolism in the body, including but not limited to: Amino Acid Disorders Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2013-02-08 13:02:17 Genetic genealogy Inborn errors of carbohydrate metabolism Hepatology Pediatrics Inborn error of metabolism Isovaleric acidemia Propionic acidemia Methylmalonic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
143	MISSOURI DEPARTMENT OF HEALTH Add to Reading List Source URL: health.mo.gov Language: English - Date: 2013-08-16 15:32:03 Medical genetics Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Maple syrup urine disease University of Missouri Health Care Medicaid Department of Health Health Rare diseases Genetic genealogy
144	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
145	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
146	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
147	Microsoft Word - Current News on Expanded Newborn Screening[removed]doc Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 12:19:04 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Inborn error of lipid metabolism Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
148	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
149	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
150	Rhode Island screens babies for 28 health conditions and hearing loss. The conditions are grouped in the categories explained below, and a list of all the conditions is on the other side of this card. Early detection and Add to Reading List Source URL: www.health.ri.gov Language: English - Date: 2014-06-27 15:48:15 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Biotinidase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Biotin Health Rare diseases Genetic genealogy

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