Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Dictionary » Glutaryl-CoA dehydrogenase
 

Glutaryl-CoA dehydrogenase

Introduction: Glutaryl-CoA dehydrogenase

Description of Glutaryl-CoA dehydrogenase

Glutaryl-CoA dehydrogenase: A flavoprotein enzyme that is responsible for the catabolism of LYSINE; HYDROXYLYSINE; and TRYPTOPHAN. It catalyzes the oxidation of $GLUTARYL-$CoA to crotonoyl-CoA using FAD as a cofactor. Glutaric aciduria type I is an inborn error of metabolism due to the deficiency of glutaryl-CoA dehydrogenase.
Source: MeSH 2007

Glutaryl-CoA dehydrogenase: Related Topics

These medical condition or symptom topics may be relevant to medical information for Glutaryl-CoA dehydrogenase:

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Sclerotylosis
  • SCM
  • SCN
  • Scoditti geminiani colonna syndrome
  • Scoleces
  • Scoleciform
  • Scoliometer
  • Scoliosis
  • Scoliosis [and kyphoscoliosis], idiopathic
  • Scoliosis associated with other conditions
  • Scoliosis due to radiation
  • Scoliosis with unilateral unsegmented bar
  • Scoliosis, congenital, with unilateral unsegmented bar

    Find out more

    Search to find out more about Glutaryl-CoA dehydrogenase:

      
      
    powered by
    Google
  •  

    By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

    Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise