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Term:long QT syndrome 14
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Accession:DOID:0110655 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM1 gene on chromosome 14q32.11. (DO)
Synonyms:exact_synonym: LQT14
 primary_id: OMIM:616247
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long QT syndrome 14 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Calm1 calmodulin 1 JBrowse link 6 124,217,241 124,225,292 RGD:7240710

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Path 1
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  disease 15984
    syndrome 6094
      long QT syndrome 247
        long QT syndrome 14 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 14 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.