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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
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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

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  disease 15984
    syndrome 6094
      long QT syndrome 247
        long QT syndrome 15 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 15 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.