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Medical genetics / Argininosuccinic aciduria / Urea cycle disorder / Newborn screening / Argininosuccinate lyase / Carbamoyl phosphate synthetase I deficiency / Glutaric acidemia type 2 / Health / Rare diseases / Genetic genealogy


Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
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Document Date: 2009-02-03 16:51:23

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IndustryTerm

chemical / chemical called ammonia / elevated chemicals / energy / /

MedicalCondition

inherited urea cycle disorder / seizures / urea cycle disorders / autosomal recessive disorder / metabolic disorders / coma / /

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What is it? / /

Organization

National Urea Cycle Disorders Foundation / Save Babies Through Screening Foundation / /

Person

Arginosuccinic Acidemia / /

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Position

physician / care physician / /

ProvinceOrState

California / Pennsylvania / /

URL

http /

SocialTag