Term:Brugada syndrome 7
go back to main search page
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
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants       view all columns           Sort by:
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    syndrome 4218
      Brugada syndrome 50
        Brugada syndrome 7 1
Path 2
Term Annotations click to browse term
  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
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.