trimethylaminuria

info · Genetic

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.

Signs and symptoms

Depression
Anemia
Hypertension
Tachycardia
Recurrent pneumonia
Splenomegaly
Decreased total neutrophil count

Also known as: fish-odor syndrome