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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
 alt_id: OMIM:611820;   RDO:0015573
 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 15984
    syndrome 6094
      long QT syndrome 247
        long QT syndrome 11 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 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.