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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005259 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005259">
        <rdfs:label>obsolete Asperger syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012079 -->

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        <rdfs:label>asperger syndrome, susceptibility to, 2</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100440"/>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4882</ns5:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/asperger_syndrome_2</ns2:curated_content_resource>
        <oboInOwl:hasExactSynonym>Asperger syndrome susceptibility 2, Isolated cases</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1837697</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ASPG2</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0012079</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:332517</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:608631</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100440 -->

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        <rdfs:label>Asperger syndrome, susceptibility to</rdfs:label>
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