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    <!-- http://www.ebi.ac.uk/efo/EFO_0004689 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0004689">
        <rdfs:label>obsolete_Jervell and Lange-Nielsen syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Surdo Cardiac Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Cardioauditory Syndrome of Jervell and Lange Nielsen</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Jervell and Lange-Nielsen Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Jervell Lange Nielsen Syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>Cardioauditory Syndrome of Jervell and Lange-Nielsen</oboInOwl:hasExactSynonym>
        <ns5:reason_for_obsolescence>use  &#39;http://www.orpha.net/ORDO/Orphanet_90647&#39; instead.
New Label : Jervell and Lange-Nielsen syndrome</ns5:reason_for_obsolescence>
        <oboInOwl:hasExactSynonym>Deafness, Congenital, and Functional Heart Disease</oboInOwl:hasExactSynonym>
        <ns5:definition_citation>http://purl.bioontology.org/ontology/MSH/D029593</ns5:definition_citation>
        <oboInOwl:hasExactSynonym>Surdo-Cardiac Syndromes</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Jervell and Lange Nielsen Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Surdo-Cardiac Syndrome</oboInOwl:hasExactSynonym>
        <ns4:IAO_0100001>http://www.orpha.net/ORDO/Orphanet_90647</ns4:IAO_0100001>
        <oboInOwl:hasExactSynonym>Syndrome, Surdo-Cardiac</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Syndrome, Jervell-Lange Nielsen</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Prolonged QT Interval in EKG and Sudden Death</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>JLNS</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE-GATED POTASSIUM CHANNEL. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).</ns4:IAO_0000115>
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