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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>
    </ObjectProperty>
    


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    <!-- http://purl.obolibrary.org/obo/HP_0000486 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000486">
        <rdfs:label>Strabismus</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0009743 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0009743">
        <rdfs:label>Distichiasis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</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_0002457 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002457">
        <rdfs:label>Treacher-Collins syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000426"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015161"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015483"/>
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            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004029"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0009743"/>
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            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004029"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0000486"/>
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        </rdfs:subClassOf>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/treacher_collins_syndrome_1</ns3:curated_content_resource>
        <oboInOwl:hasExactSynonym>Treacher Collins syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>MFD1</oboInOwl:hasRelatedSynonym>
        <ns5:IAO_0000115>A congenital disorder of craniofacial development characterized by bilateral symmetrical oto-mandibular dysplasia without abnormalities of the extremities, and associated with several head and neck defects.</ns5:IAO_0000115>
        <oboInOwl:id>MONDO:0002457</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:861</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1785</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Treacher Collins Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:969026676</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>mandibulofacial dysostosis without limb anomalies</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C75018</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:2908</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:66078</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>TCOF</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:62767009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:154500</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>TCS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Franceschetti-Klein syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Treacher-Collins syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10051456</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0242387</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0009124</oboInOwl:hasDbXref>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
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        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS154500"/>
        <ns3:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0002457"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015161">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015334 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015334">
        <rdfs:label>obsolete branchial arch or oral-acral syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015368 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015368">
        <rdfs:label>obsolete neuro-ophthalmological disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015483 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015483">
        <rdfs:label>mandibulofacial dysostosis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020157 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020157">
        <rdfs:label>obsolete syndromic palpebral coloboma</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020167 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020167">
        <rdfs:label>obsolete malposition of external canthus</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020190 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020190">
        <rdfs:label>obsolete eyebrow/eyelashes distichiasis</rdfs:label>
    </Class>
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