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Newborn screening / Methylmalonic acidemia / Isovaleric acidemia / Propionic acidemia / Fatty-acid metabolism disorder / Glutaric aciduria type 1 / Glutaric acidemia type 2 / Carnitine-acylcarnitine translocase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine


SACHDNC Recommended Uniform Screening Panel1
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Document Date: 2013-05-02 18:14:46

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Company

X X X X X X X ASA / acyl-CoA / /

Facility

American College of Medical Genetics / /

MedicalCondition

core disorder / X Tyrosinemia / S disease / CIT Citrullinemia / PKU / I Tyrosinemia / III Tyrosinemia / ketoacyl-CoA thiolase deficiency / Sickle cell anemia / II Citrullinemia / cobalamin disorders / CoA carboxylase deficiency / Disorders / /

Organization

the American College / DE RED / Health Resources and Services Administration / eta / IA CPT / /

Position

Hb / adrenal hyperplasia Hb / /

ProgrammingLanguage

C / /

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