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Term:long QT syndrome 15
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Accession:DOID:0110656 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM2 gene on chromosome 2p21. (DO)
Synonyms:exact_synonym: LQT15
 primary_id: OMIM:616249;   RDO:9001639
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long QT syndrome 15 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Calm2 calmodulin 2 JBrowse link 6 11,067,675 11,080,078 RGD:8554872
RGD:7240710

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  disease 14759
    syndrome 4210
      long QT syndrome 177
        long QT syndrome 15 1
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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        Congenital Abnormalities 3137
          Cardiovascular Abnormalities 781
            congenital heart disease 730
              long QT syndrome 177
                long QT syndrome 15 1
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