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    <!-- http://purl.obolibrary.org/obo/MONDO_0100022 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100022">
        <rdfs:label>neonatal/infantile epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100023 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100023">
        <rdfs:label>self-limited familial neonatal epilepsy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100207"/>
        <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2018-06-22T23:38:16Z</dc:date>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4940</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5740</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7700</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8668</ns4:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.epilepsydiagnosis.org/syndrome/benign-fam-nonfam-infantile-overview.html</rdfs:seeAlso>
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        <rdfs:comment>Some cases have seizure onset just outside of the neonatal period (in the first 2 months of life), and the syndrome in this case is called self-limited familial neonatal-infantile epilepsy.</rdfs:comment>
        <oboInOwl:hasNarrowSynonym>self-limited familial neonatal-infantile epilepsy</oboInOwl:hasNarrowSynonym>
        <oboInOwl:id>MONDO:0100023</oboInOwl:id>
        <oboInOwl:hasExactSynonym>self-limited familial and non-familial neonatal seizures</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>A neonatal/infantile epilepsy syndrome that is characterized by the onset of seizures that start in the in the neonate between day 1 and 7 of life and are often unilateral clonic events that recur and may alternate sides from seizure to seizure. Seizures can be repetitive over hours to days. Seizures remit by 4-6 months of age. A proportion of those affected may have seizures in later life. The child is expected to have typical developmental progress.</ns4:IAO_0000115>
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        <rdfs:label>infantile-onset epilepsy</rdfs:label>
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