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    <!-- http://purl.obolibrary.org/obo/MONDO_0009519 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009519">
        <rdfs:label>letterer-Siwe disease</rdfs:label>
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        <oboInOwl:hasDbXref>MEDGEN:7311</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>multifocal multisystem Langerhans cell histiocytosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:99870</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acute and disseminated Langerhans cell histiocytosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0023381</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>acute disseminated Langerhans cell histiocytosis</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>MedDRA:10024265</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>letterer-Siwe disease</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>A multifocal, multisystem form of Langerhans-cell histiocytosis. There is involvement of multiple organ systems including the bones, skin, liver, spleen, and lymph nodes. Patients are usually infants presenting with fever, hepatosplenomegaly, lymphadenopathy, bone and skin lesions, and pancytopenia.</ns4:IAO_0000115>
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        <rdfs:label>Langerhans cell histiocytosis specific to childhood</rdfs:label>
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