FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term trimethylaminuria ID (Ontology) DOID:0080361 (Human Disease)
Definition 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.
Also Known As "fish-odor syndrome"
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 Genes
 trimethylaminuria       2
 for disease ribbon | trimethylaminuria       2
 model of | trimethylaminuria       2
Spanning Tree (Parents/Children)
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disease of metabolism
 |__inherited metabolic disorder__
autosomal genetic disease         |
 |__autosomal recessive disease___|
genetic disease                   |
 |__inherited metabolic disorder__|
                                  trimethylaminuria  2 rec.
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Is a autosomal recessive disease
inherited metabolic disorder
Part of
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Synonyms
  • "fish-odor syndrome" EXACT
Secondary IDs
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GARD:6447
MESH:C536561
MIM:602079
ORDO:468726