Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01488355n
Noun Concept
PT
No term available
EN
A broad classification for genetic disorders that result from an inability of the body to produce or utilize an enzyme or transport protein that is required to oxidize fatty acids. Wikipedia
Relations
Sources
IS A
doença
EN
Inborn error of lipid metabolism
HAS KIND
EN
Very long-chain acyl-coenzyme A dehydrogenase deficiency
EN
short-chain acyl-coenzyme A dehydrogenase deficiency
EN
2,4 Dienoyl-CoA reductase deficiency
EN
Medium-chain acyl-coenzyme A dehydrogenase deficiency
EN
beta oxidation defect
+1 relations
HEALTH SPECIALTY
endocrinologia

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License