ONTOLOGY REPORT - ANNOTATIONS


Term:long QT syndrome 11
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Accession:DOID:0110652 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2. (DO)
Synonyms:exact_synonym: LQT11
 primary_id: MESH:C567513;   RDO:0015573
 alt_id: OMIM:611820
 xref: GARD:10437
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long QT syndrome 11 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Akap9 A-kinase anchoring protein 9 JBrowse link 4 27,195,346 27,331,582 RGD:7240710
RGD:8554872

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  disease 14926
    syndrome 4715
      long QT syndrome 176
        long QT syndrome 11 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 11 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.