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ONTOLOGY REPORT - ANNOTATIONS


Term:trimethylaminuria
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Accession:DOID:0080361 term browser browse the term
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. (DO)
Synonyms:exact_synonym: Fish malodor syndrome;   TMAU;   TMAuria;   fish odor syndrome;   stale fish syndrome
 primary_id: MESH:C536561
 alt_id: DOID:9006128;   OMIM:602079;   RDO:0002180
 xref: GARD:6447;   ORDO:468726
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trimethylaminuria term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fmo3 flavin containing dimethylaniline monoxygenase 3 JBrowse link 13 80,837,418 80,856,214 RGD:7240710
RGD:8554872
RGD:11554173

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Path 1
Term Annotations click to browse term
  disease 16022
    Nutritional and Metabolic Diseases 4644
      disease of metabolism 4644
        inherited metabolic disorder 2179
          trimethylaminuria 1
Path 2
Term Annotations click to browse term
  disease 16022
    Developmental Diseases 9336
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8164
        genetic disease 7688
          monogenic disease 5446
            autosomal genetic disease 4409
              autosomal recessive disease 2386
                trimethylaminuria 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.