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bn:01488355n
Noun Concept
NL
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
ziekte
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
medium chain acyl co-enzym-A dehydrogenase-deficiëntie
EN
beta oxidation defect
+1 relations
HEALTH SPECIALTY
endocrinologie

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