Back to Results
First PageMeta Content
3-hydroxy-3-methylglutaryl-CoA lyase deficiency / Genetic genealogy / 3-hydroxy-3-methylglutaryl-CoA lyase / Newborn screening / Protein families / Fatty-acid metabolism disorder / HMG-CoA reductase / Health / Rare diseases / Medicine


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

Document Date: 2009-02-03 16:51:10


Open Document

File Size: 19,04 KB

Share Result on Facebook

City

Plymouth / /

Country

Saudi Arabia / /

/

/

IndustryTerm

elevated chemicals / chemical / /

MedicalCondition

inherited organic acid disorder / CoA Lyase Deficiency / frequency This disorder / seizures / vomiting / disorder / diarrhea / autosomal recessive disorder / metabolic disorders / disorders / rare organic acid disorder / /

Movie

What is it? / /

Organization

Organic Acidemia Association / Save Babies Through Screening Foundation / /

/

Position

care physician / physician / /

ProvinceOrState

Minnesota / Pennsylvania / /

URL

http /

SocialTag