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ONTOLOGY REPORT - ANNOTATIONS


Term:long QT syndrome 13
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Accession:DOID:0110654 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNJ5 gene on chromosome 11q24.3. (DO)
Synonyms:exact_synonym: LQT13
 primary_id: OMIM:613485
 alt_id: RDO:0015807
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long QT syndrome 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kcnj5 potassium inwardly-rectifying channel, subfamily J, member 5 JBrowse link 8 33,435,493 33,463,410 RGD:7240710
RGD:8554872

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Term Annotations click to browse term
  disease 15984
    syndrome 6094
      long QT syndrome 247
        long QT syndrome 13 1
Path 2
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  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          monogenic disease 5382
            autosomal genetic disease 4348
              autosomal dominant disease 2713
                long QT syndrome 13 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.