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;   RDO:0015807
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long QT syndrome 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kcnj5 potassium voltage-gated channel subfamily J member 5 JBrowse link 8 33,435,493 33,463,410 RGD:7240710
RGD:8554872

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  disease 14926
    syndrome 4715
      long QT syndrome 176
        long QT syndrome 13 1
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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        Congenital Abnormalities 3200
          Cardiovascular Abnormalities 782
            congenital heart disease 731
              long QT syndrome 176
                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.