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    <!-- http://purl.obolibrary.org/obo/MONDO_0005429 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005429">
        <rdfs:label>prion disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005560"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0024619"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/prion_disease</ns4:curated_content_resource>
        <oboInOwl:id>MONDO:0005429</oboInOwl:id>
        <ns3:IAO_0000115>A transmissible disease that is caused by a protein that is able to induce abnormal folding of normal cellular proteins, leading to characteristic spongiform brain changes, which are associated with neuronal loss without an inflammatory response. Such disorders have typically long incubation periods, but are then generally rapidly progressive and are uniformly fatal.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>DOID:649</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D017096</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C128346</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0024183</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200186</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>spongiform encephalopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:046.19</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0162534</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:230284004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:56445</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:0004720</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005560 -->

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        <rdfs:label>brain disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024619 -->

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        <rdfs:label>central nervous system infectious disorder</rdfs:label>
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        <rdfs:label>obsolete_prion disease</rdfs:label>
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