OBO ID: DOID:0080361
Term Name: trimethylaminuria Search Ontology:
Synonyms:
  • fish-odor syndrome
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. https://ghr.nlm.nih.gov/condition/trimethylaminuria
References:
Ontology: Human Disease   (DOID:0080361)
OTHER trimethylaminuria PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FMO3 Trimethylaminuria 602079
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None