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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#InverseFunctionalProperty"/>
        <rdfs:label>has characteristic</rdfs:label>
        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010837 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010837">
        <rdfs:label>primary hyperparathyroidism</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016166 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016166">
        <rdfs:label>hereditary hyperparathyroidism</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016365 -->

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        <rdfs:label>familial primary hyperparathyroidism</rdfs:label>
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        <oboInOwl:hasDbXref>icd11.foundation:1186866066</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2207</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0271846</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hereditary primary hyperparathyroidism (disease)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:543605</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0016365</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0002837</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual&#39;s genome.</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021152 -->

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        <rdfs:label>inherited</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021360 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021360">
        <rdfs:label>tumor of parathyroid gland</rdfs:label>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



