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    <!-- http://purl.obolibrary.org/obo/MONDO_0002637 -->

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        <rdfs:label>histiocytosis</rdfs:label>
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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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        <oboInOwl:hasDbXref>GARD:0008231</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SCTID:127069007</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0015531</oboInOwl:id>
        <oboInOwl:hasDbXref>ICD9:288.4</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:4330</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:157987</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; juvenile XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES).</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017368 -->

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        <rdfs:label>Langerhans cell histiocytosis</rdfs:label>
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