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ONTOLOGY REPORT - ANNOTATIONS


Term:Brugada syndrome 6
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Accession:DOID:0110223 term browser browse the term
Definition:A Brugada syndrome that has material basis in heterozygous mutation in the KCNE3 gene on chromosome 11q13. (DO)
Synonyms:exact_synonym: BRGDA6
 primary_id: MESH:C567735
 alt_id: OMIM:613119;   RDO:0015723
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Brugada syndrome 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kcne3 potassium voltage-gated channel subfamily E regulatory subunit 3 JBrowse link 1 165,189,934 165,196,949 RGD:7240710
RGD:8554872

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Path 1
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  disease 15590
    syndrome 5131
      Brugada syndrome 51
        Brugada syndrome 6 1
Path 2
Term Annotations click to browse term
  disease 15590
    Developmental Diseases 8723
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7503
        genetic disease 6993
          monogenic disease 4551
            Brugada syndrome 51
              Brugada syndrome 6 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.