MeSH Browser

MeSH Supplementary: Trimethylaminuria
Unique ID: C536561
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536561
Entry Term(s): Fish malodor syndrome; Fish odor syndrome; Fish-Odor Syndrome; Stale Fish Syndrome; TMAuria
Registry Numbers: 0
Heading Mapped to: *Metabolism, Inborn Errors; Methylamines / urine
Frequency: 48
Note: 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
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Concept UI: M0531022
Registry Numbers: 0
Terms: Trimethylaminuria Preferred Term
Term UI T739729
Date02/24/2009
LexicalTag NON
ThesaurusID; Fish odor syndrome
Term UI T739731
Date02/24/2009
LexicalTag NON
ThesaurusID; Fish malodor syndrome
Term UI T739732
Date02/24/2009
LexicalTag NON
ThesaurusID; Fish-Odor Syndrome
Term UI T801553
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Stale Fish Syndrome
Term UI T842606
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); TMAuria
Term UI T844348
Date05/17/2013
LexicalTag NON
ThesaurusID NLM (2014)

Trimethylaminuria MeSH Supplementary Concept Data 2025