![Medical genetics / Fatty-acid metabolism disorder / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hyperammonemia / Carnitine / Isovaleric acidemia / Health / Rare diseases / Genetic genealogy Medical genetics / Fatty-acid metabolism disorder / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hyperammonemia / Carnitine / Isovaleric acidemia / Health / Rare diseases / Genetic genealogy](https://www.pdfsearch.io/img/68d13ef1e8afd2dd7a2009224c630b40.jpg)
| Document Date: 2011-02-25 12:37:37 Open Document File Size: 51,06 KBShare Result on Facebook
City HART LANE NASHVILLE / / Company mol/L Asa / Methionine (under validation) Ornithine Asa / Argininosuccinic Acid Asa / / / Facility Tennessee Department of Health Newborn Screening laboratory / / / MedicalCondition Nonketotic Hyperglycinemia Homocystinuria / Citrin Deficiency / diseases / respective disorders / Arginase Deficiency / disorder 3Hydroxyacyl CoA dehydrogenase deficiency / Argininosuccinate Lyase Deficiency / Arginosuccinate Synthetase Deficiency / / Organization MADD / DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM / Department of Health Newborn Screening / / Person Thomas Childs / Christine D. Mckeever Newborn Screening / Christine McKeever / / / Position Manager Date / Division Manager/MSMS Manager / / Product C5 / Glycine / C16 / / ProvinceOrState Tennessee / / Technology Alpha / /
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