| Term Name: | trimethylaminuria |
|---|---|
| Synonyms: | fish-odor syndrome |
| Definition: | An inherited metabolic disorder characterized by the inability to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24. |
| Ontology: | Human Disease [DOID:0080361] ( DOID:0080361 ) |