Back to Results
First PageMeta Content
Genetic genealogy / Glutaric acidemia type 2 / Fatty-acid metabolism disorder / Glutaric aciduria type 1 / Newborn screening / Fatty acid metabolism / Propionic acidemia / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine


Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Add to Reading List

Document Date: 2009-02-03 16:51:42

Open Document

File Size: 19,46 KB

Share Result on Facebook

Company

FOD (Fatty Oxidation Disorder) Family Support Group / /

/

/

IndustryTerm

elevated chemicals / food / energy / /

MedicalCondition

acyl-CoA Dehydrogenase Deficiency / inherited fatty acid oxidation disorder / autosomal recessive disorder / rare fatty acid oxidation disorder / metabolic disorders / liver disease / Fatty Oxidation Disorder / /

Movie

What is it? / /

Organization

United Mitochondrial Disease Foundation / Save Babies Through Screening Foundation / /

/

Position

physician / care physician / /

ProvinceOrState

Pennsylvania / /

URL

http /

SocialTag