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    <!-- http://purl.obolibrary.org/obo/MONDO_0020072 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020072">
        <rdfs:label>childhood-onset epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020073 -->

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        <rdfs:label>obsolete adolescent-onset epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020074 -->

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        <oboInOwl:hasDbXref>SCTID:267581004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:199732</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>PME</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>familial progressive myoclonic epilepsy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C0751778</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>progressive myoclonus epilepsy</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>GARD:0007140</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A rare group of disorders characterized by the development of myoclonic and tonic-clonic epileptic seizures associated with progressive degeneration of the nervous system.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>NANDO:1200953</oboInOwl:hasDbXref>
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