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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
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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_0005046 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005046">
        <rdfs:label>immune system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021094 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021094">
        <rdfs:label>immunodeficiency disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
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        <oboInOwl:hasDbXref>OMIMPS:300755</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>immunodeficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C3131</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:7034</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>immunodeficiency disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:2100204</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:279.3</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>Disease in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C0021051</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:234532001</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>immuno-deficiency</oboInOwl:hasExactSynonym>
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