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    <!-- http://purl.obolibrary.org/obo/MONDO_0005087 -->

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        <rdfs:label>respiratory system disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018310 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018310">
        <rdfs:label>Langerhans cell histiocytosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020517 -->

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        <rdfs:label>eosinophilic granuloma</rdfs:label>
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        <oboInOwl:hasExactSynonym>eosinophilic xanthomatous granuloma</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NCIT:C3016</oboInOwl:hasDbXref>
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        <ns3:IAO_0000115>A clinical variant of Langerhans cell histiocytosis characterized by unifocal involvement of a bone (most often), skin, or lung. Patients are usually older children or adults usually presenting with a lytic bone lesion. The etiology is unknown. Morphologically, eosinophilic granuloma is characterized by the presence of Langerhans cells in a characteristic milieu which includes histiocytes, eosinophils, neutrophils, and small, mature lymphocytes.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>ICDO:9752/1</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:99871</oboInOwl:hasDbXref>
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