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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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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_0100020 -->

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        <rdfs:label>atypical childhood epilepsy with centrotemporal spikes</rdfs:label>
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        <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2018-06-22T22:43:29Z</dc:date>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7700</ns3:IAO_0000233>
        <rdfs:comment>Reason of obsoletion: out of scope - MONDO:excludeHistoricalDisease. Term to consider: -</rdfs:comment>
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        <oboInOwl:hasExactSynonym>atonic-benign childhood epilepsy with centrotemporal spikes</oboInOwl:hasExactSynonym>
        <ns3:IAO_0006012>2024-09-01</ns3:IAO_0006012>
        <oboInOwl:hasExactSynonym>pseudo-Lennox syndrome</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>A childhood-onset epilepsy that is characterized by frequent seizures of multiple types, including nocturnal focal motor and fronto-parietal opercular seizures, and daytime focal motor seizures with negative myoclonus and atypical absence seizures. Centrotemporal sharp waves are seen on EEG. During the phase of the epilepsy when seizures are frequent, neuropsychological deficits and motor impairment may be present. These deficits improve when seizures remit.</ns3:IAO_0000115>
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