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    <!-- http://purl.obolibrary.org/obo/MONDO_0011229 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011229">
        <rdfs:label>ethylmalonic encephalopathy</rdfs:label>
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        <ns3:IAO_0000115>Ethylmalonic acid encephalopathy (EE) is defined by elevated excretion of ethylmalonic acid (EMA) with recurrent petechiae, orthostatic acrocyanosis and chronic diarrhea associated with neurodevelopmental delay, psychomotor regression and hypotonia with brain magnetic resonance imaging (MRI) abnormalities.</ns3:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>EPEMA syndrome</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>encephalopathy, ethylmalonic</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>eme</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0044970 -->

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        <rdfs:label>mitochondrial disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100198 -->

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        <rdfs:label>Mendelian encephalopathy</rdfs:label>
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        <rdfs:label>obsolete_ethylmalonic encephalopathy</rdfs:label>
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