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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004029">
        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0004349 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0004349">
        <rdfs:label>Reduced bone mineral density</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0009814 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009814">
        <rdfs:label>osteopenia-intellectual disability-sparse hair syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004029"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0004349"/>
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        </rdfs:subClassOf>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5588</ns5:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/osteopenia_and_sparse_hair</ns3:curated_content_resource>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/osteopenia_intellectual_disability_sparse_hair_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasExactSynonym>Kaler-Garrity-Stern syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:259690</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1850140</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:732954002</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537706</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>osteopenia mental retardation sparse hair</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0000354</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>osteopenia and sparse hair</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>osteopenia intellectual disability sparse hair</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0009814</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>Kaler Garrity Stern syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:337979</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Kaler-Garrity-Stern syndrome is a rare syndrome, described in two sisters of Mennonite descent, characterized by sparse hair, osteopenia, intellectual disability, minor facial abnormalities, joint laxity and hypotonia. There have been no further descriptions in the literature since 1992.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:2324</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/337979"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C537706"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/732954002"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1850140"/>
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        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019704"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <skos:exactMatch rdf:resource="https://omim.org/entry/259690"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019704 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019704">
        <rdfs:label>obsolete primary bone dysplasia with decreased bone density</rdfs:label>
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