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    <!-- http://purl.obolibrary.org/obo/MONDO_0005579 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005579">
        <rdfs:label>idiopathic generalized epilepsy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009696 -->

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        <rdfs:label>juvenile myoclonic epilepsy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011875 -->

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        <rdfs:label>epilepsy, idiopathic generalized, susceptibility to, 11</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C2750893</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>generalized epilepsy caused by mutation in CLCN2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>CLCN2 generalized epilepsy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>EIG11</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:416407</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>CLCN2 generalised epilepsy</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasRelatedSynonym>susceptibility to idiopathic generalised epilepsy 11</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:607628</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the CLCN2 gene.</ns4:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011876 -->

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