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ONTOLOGY REPORT - ANNOTATIONS


Term:Brugada syndrome 7
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Accession:DOID:0110224 term browser browse the term
Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN3B gene on chromosome 11q24. (DO)
Synonyms:exact_synonym: BRGDA7
 narrow_synonym: ATFB16;   ATRIAL FIBRILLATION, FAMILIAL, 16
 primary_id: MESH:C567734
 alt_id: OMIM:613120;   RDO:0015722
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Brugada syndrome 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Scn3b sodium voltage-gated channel beta subunit 3 JBrowse link 8 44,136,413 44,159,011 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    syndrome 6141
      Brugada syndrome 65
        Brugada syndrome 7 1
Path 2
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15273
      cardiovascular system disease 4374
        heart disease 2600
          Cardiac Arrhythmias 586
            atrial fibrillation 211
              familial atrial fibrillation 36
                Familial Atrial Fibrillation 16 1
                  Brugada syndrome 7 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.