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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>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009506 -->

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        <rdfs:label>specific granule deficiency</rdfs:label>
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        <oboInOwl:hasExactSynonym>neutrophil-specific granule deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C562873</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>recurrent infection due to specific granule deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:140766</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:245480</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:169142</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0009506</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C0398593</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:234587000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>specific granule deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>SGD</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0010778</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/234587000"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0398593"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015978 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015978">
        <rdfs:label>functional neutrophil defect</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024626 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0024626">
        <rdfs:label>defective phagocytic cell engulfment</rdfs:label>
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