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Genetic 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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Document Date: 2013-07-08 12:47:26

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City

Salt Lake City / /

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MedicalCondition

recessive disorder / Hemoglobinopathies / Severe Combined Imunodeficiency disorder / Short Chain Acyl-CoA Dehydrogenase Deficiency / Tyrosinemia Fatty Acid Oxidation Disorders / Congenital Adrenal Hyperplasia / CoA Dehydrogenase Deficiency / CoA Lyase Deficiency / Beta-Ketothiolase Deficiency / recessive disorders / genetic disorder / Deficiency Organic Acid Disorders / Congenital Hypothyroidism / Very long Chain Acyl-CoA Dehydrogenase Deficiency / body fight infections / Citrullinemia / Argininosuccinate Lyase Deficiency / Isobutyryl CoA Dehydrogenase Deficiency / Alpha Thalassemia / Galactosemia / protein deficiency / disorder / PKU / Sickle cell disease / Carnitine-Acylcarnitine Translocase Deficiency / SCID / Actual disease / Deficiency / Phenylketonuria / Medium Chain Acyl-CoA Dehydrogenase Deficiency / Multiple Carboxylase Deficiency / Biotinidase deficiency / Hydroxyacyl-CoA Dehydrogenase Deficiency / Multiple Acyl-CoA Dehydrogenase Deficiency / Arginase Deficiency / Cystic Fibrosis / recessively inherited disorders / Maple Syrup Urine Disease / disorders / enzyme deficiency / Homocystinuria / /

Organization

MADD / /

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Product

FS / /

ProvinceOrState

Utah / /

Technology

Alpha / /

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