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    <!-- http://purl.obolibrary.org/obo/MONDO_0005579 -->

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        <rdfs:label>idiopathic generalized epilepsy</rdfs:label>
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        <rdfs:label>obsolete ARX-related epileptic encephalopathy</rdfs:label>
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        <rdfs:label>disorder of GPI anchor biosynthesis</rdfs:label>
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        <rdfs:label>neonatal/infantile epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100062 -->

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        <rdfs:label>genetic developmental and epileptic encephalopathy</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8274</ns4:IAO_0000233>
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        <oboInOwl:hasDbXref>DOID:0112202</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:345.10</oboInOwl:hasDbXref>
        <oboInOwl:hasBroadSynonym>developmental and epileptic encephalopathy</oboInOwl:hasBroadSynonym>
        <ns4:IAO_0000115>A complex neurodevelopmental disorder characterized by a range of developmental delays and epileptic encephalopathy phenotypes. Seizure onset is variable and intellectual disability is variable in presence and severity.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>NANDO:1200593</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>OMIMPS:308350</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100500 -->

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