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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 14759
    syndrome 4210
      long QT syndrome 177
        long QT syndrome 11 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 11 1
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