Preferred Label : Glutaryl-CoA dehydrogenase;
MeSH definition : 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.;
MeSH synonym : glutaryl coenzyme a dehydrogenase; dehydrogenase, glutaryl-coa; glutaryl-coenzyme a dehydrogenase; dehydrogenase, glutaryl-coenzyme a; coa dehydrogenase, glutaryl; dehydrogenase, glutaryl coa; glutaryl CoA dehydrogenase;
MeSH Related Number : 37255-38-2 (CRN);
Registry Number MeSH : EC 1.3.99.7; EC 1.3.8.6;
Is substance : O;
UNII : EC 1.3.8.6;
Origin ID : D050770;
UMLS CUI : C0061510;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
Record concept(s)
Related MeSH Supplementary Concept(s)
See also inter- (CISMeF)
Semantic type(s)
UMLS correspondences (same concept)
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.
https://www.has-sante.fr/jcms/p_3262535/fr/acidurie-glutarique-type-1
2021
false
false
false
France
case management
amino acid metabolism, inborn errors
amino acid metabolism, inborn errors
brain diseases, metabolic
brain diseases, metabolic
brain diseases, metabolic
brain diseases, metabolic
amino acid metabolism, inborn errors
amino acid metabolism, inborn errors
carnitine
lysine
dietary supplements
practice guideline
Glutaric Acidemia I
amino acid metabolism, inborn errors
brain diseases, metabolic
Glutaryl-CoA dehydrogenase
---
http://publications.msss.gouv.qc.ca/msss/document-002132/
2018
Canada
algorithms
diagnosis
glutaric aciduria, type 1
Glutaric Acidemia I
patient care management
Acidemia
amino acid metabolism, inborn errors
brain diseases, metabolic
Glutaryl-CoA dehydrogenase
---
https://www.anses.fr/fr/system/files/NUT2016SA0020.pdf
2017
false
false
false
France
French
scientific and technical information
glutaric acid
Glutaric Acidemia I
nutritional disorder, nos
amino acids
child, nos
nutrition therapy
inlets
nutritional requirement
needs
relative
medical
glutaric aciduria, type 1
special
judgment
treaties
child
hereditary diseases
hereditary disease, nos
nutritional requirements
metabolic disease, nos
metabolism, inborn errors
nutritional and metabolic diseases
has assessment
Amino acid
specialists
amino acid, nos
bays
health services needs and demand
international cooperation
genetic diseases, inborn
nutritional and metabolic diseases
evaluation studies as topic
specialization
glutarates
amino acid metabolism, inborn errors
brain diseases, metabolic
Glutaryl-CoA dehydrogenase
---
http://www.ag1-23soleil.fr/
France
French
association of patients
Glutaric Acidemia I
Glutaryl-CoA dehydrogenase
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=25
2003
false
France
French
Glutaryl-CoA dehydrogenase
rare diseases
glutarates
amino acid metabolism, inborn errors
Glutaric Acidemia I
brain diseases, metabolic
scientific and technical information
---