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    <!-- http://purl.obolibrary.org/obo/MONDO_0015531 -->

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        <rdfs:label>non-Langerhans cell histiocytosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015537 -->

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        <rdfs:label>necrobiotic xanthogranuloma</rdfs:label>
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        <oboInOwl:hasDbXref>ICD9:709.8</oboInOwl:hasDbXref>
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        <ns3:IAO_0000115>A cutaneous necrobiotic disorder characterized by firm, yellow plaques or nodules, often in a periorbital distribution. It is often accompanied by an elevated erythrocyte sedimentation rate; leukopenia; and monoclonal gammopathy (IgG-kappa type) and systemic involvement.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>Orphanet:158011</oboInOwl:hasDbXref>
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