Propionic acid

Results: 80



#Item
41Medical genetics / Newborn screening / Propionic acidemia / Fatty-acid metabolism disorder / 2-Methylbutyryl-CoA dehydrogenase deficiency / Biotinidase deficiency / Isovaleric acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Methylmalonic acidemia / Health / Rare diseases / Genetic genealogy

State of Illinois Rod R. Blagojevich, Governor Department of Public Health Eric E. Whitaker, M.D., M.P.H., Director Newborn Metabolic

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Source URL: www.idph.state.il.us

Language: English - Date: 2007-07-24 10:41:11
42Genetic genealogy / Vitamin B12 / Methylmalonic acidemia / Methylmalonic acid / Acidosis / Protein / Propionic acidemia / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Medicine / Rare diseases

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

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Source URL: www.chfs.ky.gov

Language: English - Date: 2014-09-11 01:32:54
43Medical 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

Organic Acid Disorders Information for Parents  Overview

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Source URL: www.kdheks.gov

Language: English - Date: 2013-09-05 15:51:36
44Genetic genealogy / Methylmalonic acidemia / Vitamin B12 / Acidosis / Methylmalonic acid / Protein / Propionic acidemia / Glutaric aciduria type 1 / Health / Medicine / Rare diseases

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

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Source URL: www.chfs.ky.gov

Language: English - Date: 2014-09-09 03:31:10
45Medical genetics / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Fatty-acid metabolism disorder / 3-Methylcrotonyl-CoA carboxylase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Maple syrup urine disease / Health / Rare diseases / Genetic genealogy

Microsoft Word - Disorder list Jan 10

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Source URL: azdhs.gov

Language: English - Date: 2012-04-12 12:47:40
46Medical genetics / Newborn screening / Methylmalonic acidemia / Propionic acidemia / Isovaleric acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Maple syrup urine disease / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Methylmalonic acid / Health / Rare diseases / Genetic genealogy

NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation

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Source URL: azdhs.gov

Language: English - Date: 2012-04-12 12:46:51
47Medical genetics / Newborn screening / Methylmalonic acidemia / Isovaleric acidemia / Propionic acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Methylmalonic acid / Maple syrup urine disease / Acyl CoA dehydrogenase / Health / Rare diseases / Genetic genealogy

Microsoft Word - MoD Fact Sheet 2011

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Source URL: azdhs.gov

Language: English - Date: 2012-04-12 12:46:55
48Methylmalonic acidemia / Newborn screening / Isovaleric acidemia / Methylmalonic acid / Acyl CoA dehydrogenase / Maple syrup urine disease / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Propionic acidemia

Arizona Department of Health Services Newborn Screening Program MSMS Pilot Project – Secondary Markers Amino Acid Disorders Analytes

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Source URL: azdhs.gov

Language: English - Date: 2013-07-03 16:56:45
49Genetic genealogy / Fatty-acid metabolism disorder / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Propionic acidemia / Malonyl-CoA decarboxylase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine

Newborn Screening Program Disorders

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Source URL: health.utah.gov

Language: English - Date: 2013-07-08 12:47:26
50Medical genetics / Newborn screening / Methylmalonic acidemia / Isovaleric acidemia / Glutaric aciduria type 1 / Fatty-acid metabolism disorder / Propionic acidemia / Glutaric acidemia type 2 / Carnitine / Health / Rare diseases / Genetic genealogy

Microsoft Word - ND_Disorder List[removed]doc

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Source URL: www.ndhealth.gov

Language: English - Date: 2013-07-08 13:17:03
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