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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_etiological_subtype"/>
    


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    <!-- http://purl.obolibrary.org/obo/RO_0004030 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004030">
        <rdfs:label>disease arises from structure</rdfs:label>
        <rdfs:label>disease arises from alteration in structure</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHR_9606-chrXq26 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHR_9606-chrXq26">
        <rdfs:label>Xq26 (Human)</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000425 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000425">
        <rdfs:label>X-linked disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010491 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010491">
        <rdfs:label>X-linked acrogigantism due to Xq26 microduplication</rdfs:label>
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        </rdfs:subClassOf>
        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3492</ns6:IAO_0000233>
        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns6:IAO_0000233>
        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7693</ns6:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/chromosome_xq263_duplication_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasExactSynonym>chromosome xq26.3 duplication syndrome, X-linked dominant</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>X-linked acrogigantism</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:300942</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial infantile gigantism due to dup(X)q(26)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>familial infantile gigantism due to Xq26 microduplication</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>chromosome Xq26.3 DUPLICATION syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0010491</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:448372</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>chromosome Xq26 microduplication syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C3891556</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>X-LAG (X-linked acrogigantism) due to dup(X)q(26)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:856021</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:300373</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:768472004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0018433</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017009 -->

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        <rdfs:label>partial duplication of the short arm of chromosome X</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017010 -->

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        <rdfs:label>partial duplication of the long arm of chromosome X</rdfs:label>
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