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

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Path 1
Term Annotations click to browse term
  disease 14823
    syndrome 4218
      Brugada syndrome 50
        Brugada syndrome 7 1
Path 2
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  disease 14823
    disease of anatomical entity 13997
      cardiovascular system disease 4055
        heart disease 2226
          heart conduction disease 263
            atrial fibrillation 189
              familial atrial fibrillation 16
                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.