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    <!-- http://purl.obolibrary.org/obo/MONDO_0018614 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018614">
        <rdfs:label>undetermined early-onset epileptic encephalopathy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019216"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020070"/>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4985</ns3:IAO_0000233>
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        <oboInOwl:hasExactSynonym>non-specific early-onset epileptic encephalopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0018614</oboInOwl:id>
        <oboInOwl:hasExactSynonym>undetermined early-onset epileptic encephalopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1826068</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C5680057</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:442835</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0015028</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A rare infantile epilepsy syndrome characterized by early onset of seizures of variable type and severity, potentially associated with a spectrum of clinical signs and symptoms including delay or lack of psychomotor development, intellectual disability, poor or absent speech development, behavioral abnormalities, hypotonia, movement disorders, spasticity, microcephaly, and dysmorphic facial features, among others. Brain imaging findings are also variable and may include cerebral atrophy or white matter abnormalities.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>undetermined EOEE</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019216 -->

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        <rdfs:label>inborn disorder of amino acid transport</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020070 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020070">
        <rdfs:label>neonatal epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020071 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020071">
        <rdfs:label>infantile epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100545 -->

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        <rdfs:label>hereditary neurological disease</rdfs:label>
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