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    <!-- 
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    <AnnotationProperty rdf:about="https://www.wikidata.org/wiki/Property:P828"/>
    <AnnotationProperty rdf:about="https://www.wikidata.org/wiki/Property:P5806"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/GSSO_006974 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GSSO_006974">
        <rdfs:label xml:lang="en">48,XYYY syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/GSSO_006992"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/GSSO_012485"/>
        <ns2:P5806 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">http://purl.bioontology.org/ontology/SNOMEDCT/733625003</ns2:P5806>
        <ns3:IAO_0000115 xml:lang="en">A rare Y chromosome number anomaly that affects only males. The disease has characteristics of mild-moderate developmental delay (especially speech), normal to mild intellectual disability, large, irregular teeth with poor enamel, tall stature and acne. Radioulnar stenosis and clinodactyly have also been associated. Boys generally present normal genitalia, while hypogonadism and infertility is frequently reported in adult males.</ns3:IAO_0000115>
        <oboInOwl:hasSynonym xml:lang="en">XYYY syndrome</oboInOwl:hasSynonym>
        <ns2:P828 rdf:resource="http://purl.obolibrary.org/obo/GSSO_009572"/>
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    <!-- http://purl.obolibrary.org/obo/GSSO_006992 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GSSO_006992">
        <rdfs:label xml:lang="en">chromosomal gain syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/GSSO_009572 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GSSO_009572">
        <rdfs:label xml:lang="en">48,XYYY</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/GSSO_012485 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GSSO_012485">
        <rdfs:label xml:lang="en">allosomal chromosomal syndrome</rdfs:label>
    </Class>
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