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    <!-- http://purl.obolibrary.org/obo/MONDO_0006530 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006530">
        <rdfs:label>cholesteatoma</rdfs:label>
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        <oboInOwl:hasDbXref>ICD9:385.30</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0008373</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SCTID:363668000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C2944</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A pathologic process characterized by the proliferation of keratinizing squamous epithelium resulting in the accumulation of keratin and cells in the middle ear and/or mastoid. It may be congenital or acquired. If left untreated, it may increase in size and destroy adjacent structures.</ns3:IAO_0000115>
        <oboInOwl:id>MONDO:0006530</oboInOwl:id>
        <oboInOwl:hasExactSynonym>cholesteatoma (disease)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:3043</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>primary acquired cholesteatoma (type)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>secondary acquired cholesteatoma (type)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>congenital cholesteatoma (type)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>DOID:869</oboInOwl:hasDbXref>
        <ns3:IAO_0000589>cholesteatoma (disease)</ns3:IAO_0000589>
        <oboInOwl:hasDbXref>MESH:D002781</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:1000675</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>HP:0009797</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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