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    <!-- http://purl.obolibrary.org/obo/MONDO_0005151 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005151">
        <rdfs:label>endocrine system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015127 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015127">
        <rdfs:label>pituitary deficiency</rdfs:label>
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        <oboInOwl:hasDbXref>GARD:0019801</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:292840069</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0015127</oboInOwl:id>
        <rdfs:comment>Editor note: in ORDO, Orphanet:101957 is classified as genetic, yet has acquired subtypes</rdfs:comment>
        <oboInOwl:hasDbXref>Orphanet:101957</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_101957"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015968 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015968">
        <rdfs:label>obsolete rare genetic hypothalamic or pituitary disease</rdfs:label>
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