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        <rdfs:label>has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
        <equivalentClass>
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                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021127"/>
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        <oboInOwl:hasDbXref>UMLS:C0039082</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:225</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MESH:D013577</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:11688</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>syndrome associated with disease or disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OGMS:0000086</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>cluster, symptom</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition.</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011348 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011348">
        <rdfs:label>non-syndromic polydactyly</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019530 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019530">
        <rdfs:label>non-syndromic syndactyly</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021127 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021127">
        <rdfs:label>has a syndromic presentation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700096 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700096">
        <rdfs:label>human disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_7770006 -->

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