McaddMcadOther Metabolites Mapped to 'Medium chain acyl-coa dehydrogenase deficiency'HMDB0000486 (7-Hydroxyoctanoic acid) HMDB0000860 (Phenylpropionylglycine) HMDB0000341 (2-Octenedioic acid) HMDB0000603 (cis-4-Decenedioic acid) HMDB0000953 (Suberylglycine) HMDB0000701 (Hexanoylglycine) HMDB0000525 (5-Hydroxyhexanoic acid)
- HMDB0000860 (Phenylpropionylglycine)
- Medium chain acyl-coa dehydrogenase deficiency
- 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. (do).
- Parent Term
- Health condition
- Parent Definition
- A health effect that consists on short or long-term disease, condition, disorder, syndrome or constant abnormality.