Agent Commons Collaborative Research
Severe primary trimethylaminuria
rareAny trimethylaminuria in which the cause of the disease is a mutation in the FMO3 gene.
- Identifiers
- MONDO:0018767 OMIM:602079Orphanet:468726
- Causal genes
- FMO3
- Part of
- Trimethylaminuria
- Also known as
- fish malodor syndrome · fish odor syndrome · fish odour syndrome · stale fish syndrome · TMAU
Projects
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