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    <!-- http://purl.obolibrary.org/obo/MONDO_0002052 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002052">
        <rdfs:label>lymphadenitis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012727 -->

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        <oboInOwl:hasDbXref>DOID:13378</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C34825</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:75053002</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>icd11.foundation:540285662</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acute febrile mucocutaneous lymph node syndrome [MCLS]</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Kawasaki syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>mucocutaneous lymph node syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D009080</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:10118</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2331</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:611775</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>A rare inflammatory disease characterized by an acute febrile, systemic, self-limiting, medium-vessel vasculitis primarily affecting children. It often causes acute coronary arteritis which is associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>infantile polyarteritis nodosa</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0006816</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acute febrile mucocutaneous lymph node syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10023320</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018882 -->

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        <rdfs:label>vasculitis</rdfs:label>
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