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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

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        <rdfs:label>syndromic intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017975 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017975">
        <rdfs:label>sex chromosome disorder of sex development</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019929 -->

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        <rdfs:label>49,XXXXY syndrome</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns4:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/5679/49xxxxy-syndrome</rdfs:seeAlso>
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        <oboInOwl:hasDbXref>ICD9:758.81</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>The 49,XXXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of three extra X chromosomes in males.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>GARD:0005679</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:96264</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>XXXXY syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:38847009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:75573</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C185635</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0265499</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700027 -->

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        <rdfs:label>chromosome X disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700085 -->

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        <rdfs:label>pentasomy</rdfs:label>
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