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
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trimethylaminuria term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fmo3 flavin containing monooxygenase 3 JBrowse link 13 80,837,418 80,856,214 RGD:7240710
RGD:8554872
RGD:11554173

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  disease 14823
    Nutritional and Metabolic Diseases 4250
      disease of metabolism 4250
        inherited metabolic disorder 1808
          trimethylaminuria 1
Path 2
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  disease 14823
    Developmental Diseases 7637
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6675
        genetic disease 5920
          monogenic disease 2859
            autosomal genetic disease 2140
              autosomal recessive disease 1257
                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.