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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0011675 -->

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        <rdfs:label>Arrhythmia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000591 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000591">
        <rdfs:label>intrinsic cardiomyopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000992 -->

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        <rdfs:label>heart conduction disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002442 -->

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        <rdfs:label>long QT syndrome</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/10434</ns5:IAO_0000233>
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        <oboInOwl:hasDbXref>ICD10CM:I45.81</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ventricular arrhythmia associated with long QT syndrome</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>A cardiac rhythm disease characterized by prolongation of the corrected QT (QTc) interval on the surface electrocardiogram, associated with precipitation of torsade de pointes (TdP), a polymorphic ventricular tachycardia that may cause sudden death. It is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia. It may be congenital or, more frequently, acquired. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:D008133</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200228</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0027044</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>long QT syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:2100053</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:2843</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C34786</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0002442</oboInOwl:id>
        <oboInOwl:hasDbXref>ICD9:426.82</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:44193</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005453 -->

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