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ONTOLOGY REPORT - ANNOTATIONS


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 14924
    syndrome 4713
      long QT syndrome 176
        long QT syndrome 15 1
Path 2
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  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        Congenital Abnormalities 3188
          Cardiovascular Abnormalities 781
            congenital heart disease 730
              long QT syndrome 176
                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.