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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#InverseFunctionalProperty"/>
        <rdfs:label>has characteristic</rdfs:label>
        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006522 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006522">
        <rdfs:label>acquired keratosis</rdfs:label>
        <equivalentClass>
            <Class>
                <intersectionOf rdf:parseType="Collection">
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        <oboInOwl:hasDbXref>SCTID:400166009</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acquired keratosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>keratoderma, acquired</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C34746</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:13072</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0006522</oboInOwl:id>
        <ns4:IAO_0000115>Focal or diffuse thickening of the skin not inherited as a primary genetic disorder. Causes include inflammatory skin disorders, infectious disorders, lymphedema, and medications.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:44016</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:701.1</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acquired keratoderma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0022581</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006566 -->

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        <rdfs:label>keratosis</rdfs:label>
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