DISEASES

Disease-gene associations mined from literature

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,  fish-odor syndromes ...