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DOID:0080153 - medium chain acyl-CoA dehydrogenase deficiency
Disease Ontology Definition:A lipid metabolism disorder that is characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase that results in the inability to convert medium chain fatty acids to energy, particularly during fasting.
Synonyms:
Xenbase Genes : acadm
MONDO:0008721 - medium chain acyl-CoA dehydrogenase deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
lipid metabolism disorder (is_a)