ONTOLOGY REPORT - ANNOTATIONS


Term:long QT syndrome 10
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Accession:DOID:0110651 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. (DO)
Synonyms:exact_synonym: LQT10
 primary_id: MESH:C567514
 alt_id: OMIM:611819;   RDO:0015574
 xref: GARD:10436
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long QT syndrome 10 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Scn4b sodium voltage-gated channel beta subunit 4 JBrowse link 8 49,441,106 49,456,279 RGD:7240710
RGD:8554872
Familial Atrial Fibrillation 17 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Scn4b sodium voltage-gated channel beta subunit 4 JBrowse link 8 49,441,106 49,456,279 RGD:8554872

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  disease 14926
    syndrome 4715
      long QT syndrome 176
        long QT syndrome 10 1
          Familial Atrial Fibrillation 17 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 10 1
                  Familial Atrial Fibrillation 17 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.