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ONTOLOGY REPORT - ANNOTATIONS


Term:long QT syndrome 12
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Accession:DOID:0110653 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21. (DO)
Synonyms:exact_synonym: LQT12
 primary_id: MESH:C567842
 alt_id: OMIM:612955;   RDO:0015756
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long QT syndrome 12 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Snta1 syntrophin, alpha 1 JBrowse link 3 149,874,023 149,905,980 RGD:8554872
RGD:7240710

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  disease 15620
    syndrome 5159
      long QT syndrome 213
        long QT syndrome 12 1
Path 2
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  disease 15620
    Developmental Diseases 8739
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7521
        genetic disease 7009
          monogenic disease 4562
            autosomal genetic disease 3515
              autosomal dominant disease 2079
                long QT syndrome 12 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.