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ONTOLOGY REPORT - ANNOTATIONS


Term:Brugada syndrome 8
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Accession:DOID:0110225 term browser browse the term
Definition:A Brugada syndrome that has material basis in heterozygous mutation in the HCN4 gene on chromosome 15q24. (DO)
Synonyms:exact_synonym: BRGDA8
 primary_id: MESH:C567732
 alt_id: OMIM:613123;   RDO:0015720
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Brugada syndrome 8 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hcn4 hyperpolarization activated cyclic nucleotide-gated potassium channel 4 JBrowse link 8 63,599,907 63,637,327 RGD:7240710
RGD:8554872

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  disease 15590
    syndrome 5131
      Brugada syndrome 51
        Brugada syndrome 8 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 8 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.