| Document Date: 2014-08-18 18:47:48
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Company acyl-CoA / NBS Laboratory / / Currency MGA / / Facility MCH/CSHCS clinic / Clinical Laboratory Standards Institute / Laboratory Follow-Up Procedures/Requests / Laboratory Testing / / IndustryTerm Medium chain / electronic media / peak processing periods / appropriate protocol / received telephone notification / pickup services / required processing / pick-up services / long chain / Electronic reporting systems / / MedicalCondition classic galactosemia / Endocrine Disorders / Congenital adrenal hyperplasia / Hypermethioninenemia Hyperphenylalaninemia Maple syrup urine disease / Oxidation (FAO) Disorders / Acid (AA) Disorders / disease / Carnitine palmitoyltransferase deficiency I / electron transfer flavoprotein deficiency / urea cycle disorders / I Tyrosinemia / Sickle cell anemia / S/C anemia / Citrullinemia / Hypothyroidism Hemoglobinopathies / Trifunctional enzyme deficiency / Galactosemia / newborn disease / beta-thalassemia / Citrin deficiency / Tyrosinemia / Carnitine palmitoyltransferase deficiency II / also called argininemia / CoA reductase deficiency / PKU / Carnitine-acylcarnitine translocase deficiency / ETF deficiency / Phenylketonuria / deficiency / Biotinidase deficiency / Arginase deficiency / hydroxyacyl-CoA dehydrogenase deficiency / Cystic fibrosis / cobalamin disorders / CoA carboxylase deficiency / disorders / Homocystinuria / / Organization United Nations / Indiana State Department / Food & Drug Administration / CPT IA / Clinical Laboratory Standards Institute / / Position responsible physician / care physician / source and responsible physician / physician / midwife / Public Health Nurse / local health official / / ProvinceOrState Indiana / / Technology Genomics / /
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ATTACHMENT D Newborn Screening Laboratory Specific Products and Services Function 1: Filter Paper Kits Overview