Disorder of methylamine metabolism
MONDO:0100477An inherited metabolic disease that has its basis in the disruption of methylamine metabolic process.
2 clinical trials for this condition and its sub-types, 0 tagged with Disorder of methylamine metabolism itself.
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Browse by category →Sub-types of Disorder of methylamine metabolism
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Dimethylglycine dehydrogenase deficiency 0 trials · 2 incl. sub-types
1 sub-type
- Trimethylaminuria 2 trials Sub-types →
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Sarcosinemia 0 trials
Most studied deeper sub-types
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.