<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0015564"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:skos="http://www.w3.org/2004/02/skos/core#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns2="http://purl.obolibrary.org/obo/mondo#"
     xmlns:ns4="http://purl.obolibrary.org/obo/"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#excluded_subClassOf"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#closeMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015157 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015157">
        <rdfs:label>human herpesvirus 8-related tumor</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015564 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015564">
        <rdfs:label>Castleman disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016537"/>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/castleman_disease</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>NORD:898</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C3056</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>giant lymph node hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0015564</oboInOwl:id>
        <oboInOwl:hasDbXref>MESH:D005871</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0111157</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:207036003</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Castleman disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>angiofollicular lymphoid hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Castleman&#39;s tumor</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10050251</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0017531</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>ALNH</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Castleman&#39;s tumour</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:160</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>angiofollicular lymph hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Castleman&#39;s disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>angiofollicular lymph node hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:42211</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>AFLH</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>GLNH</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>angiofollicular ganglionic hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10CM:D47.Z2</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0012656</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Castleman disease (CD) is a benign lymphoproliferative disorder that may present as a localized or multicentric form. The clinical manifestations are heterogeneous, ranging from asymptomatic discrete lymphadenopathy to recurrent episodes of diffuse lymphadenopathy with severe systemic symptoms.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>icd11.foundation:1940989685</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1940989685"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10050251"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/42211"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D005871"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/207036003"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0017531"/>
        <skos:exactMatch rdf:resource="http://purl.bioontology.org/ontology/ICD10CM/D47.Z2"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0111157"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015157"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015757"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C3056"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_160"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015757 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015757">
        <rdfs:label>lymphoid hemopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016537 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016537">
        <rdfs:label>lymphoproliferative syndrome</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



