Trimethylaminuria

A hereditary autosomal recessive condition which results from the abnormal presence of large amounts of volatile and malodorous trimethylamine within the body. This chemical, a tertiary aliphatic AMINE, is excreted in the urine, sweat (ichthyohidrosis), and breath, which take on the offensive odor of decaying fish. Mutations in the FMO3 gene have been identified. OMIM: 602079

Also Known As:

Fish malodor syndrome; Fish odor syndrome; Fish-Odor Syndrome; Stale Fish Syndrome; TMAuria

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inborn Errors Metabolism: 1183
    - Trimethylaminuria: 136
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10634
  - Inborn Errors Metabolism: 1183
    - Trimethylaminuria: 136
Organic Chemicals: 140
- Amines: 4925
  - Methylamines: 15
    - Trimethylaminuria: 136

Kiersten Riedler Selected Research

Kiersten Riedler Research Topics

Disease

Drug/Important Bio-Agent (IBA)