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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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    <!-- https://bio.scai.fraunhofer.de/ontology/epilepsy#self-limited_neonatal_seizure_and_self-limited_familial_neonatal_epilepsy -->

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        <rdfs:label>self-limited neonatal seizure and self-limited familial neonatal epilepsy</rdfs:label>
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        <ns2:fromILAE rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns2:fromILAE>
        <oboInOwl:hasDefinition>Self-limited neonatal seizures and familial neonatal epilepsy may have similar clinical and electrical features, but can be distinguished on the basis of family history. These entities may have similar genetic etiologies, with de novo mutations responsible for the lack of family history in self-limited neonatal seizures.</oboInOwl:hasDefinition>
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