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Disease Ontology Browser
trimethylaminuria (DOID:0080361)
Alliance: disease page
Synonyms: fish-odor syndrome
Alt IDs: OMIM:602079, MESH:C536561, ORDO:468726
Definition: An inherited metabolic disorder characterized by the inabilty 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
02/13/2024
MGI 6.23
The Jackson Laboratory