Human genes for trimethylaminuria
Trimethylaminuria [DOID:0080361]
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.
Synonyms: trimethylaminuria, DOID:0080361, trimethylaminurias, fish-odor syndrome, fishodor syndrome ...