Agent Commons Collaborative Research

Trimethylaminuria

rare

A rare inborn error of metabolism characterized by the presence of large amounts of trimethylamine in urine, sweat, and breath, resulting in a fishy body odor in affected individuals.

Identifiers
MONDO:0011182 Orphanet:35056
Part of
Dimethylglycine dehydrogenase deficiency
Also known as
fish malodor syndrome · fish odor syndrome · fish odour syndrome · fish-odor syndrome · stale fish syndrome

Subtypes

All diseases Rare only

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