OBO ID: DOID:0080361 |
Term Name: | trimethylaminuria | Search Ontology: | |
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Synonyms: |
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Definition: | An inherited metabolic disorder characterized by the inabilty 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. (2) | ||
References: |
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Ontology: | Human Disease ( DOID:0080361 ) |
OTHER trimethylaminuria PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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FMO3 | Trimethylaminuria |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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