Secondary trimethylaminuria
MONDO:0100041A type of trimethylaminuria that occurs as the result of treatment with large doses of dietary precursors of the offending chemical. Symptoms develop when the ability of the liver enzyme (flavin-containing monooxygenase 3) is insufficient to break down (metabolize) the excess trimethylamine.
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Trimethylaminuria
(2)
Dimethylglycine dehydrogenase deficiency
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.