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    <!-- http://purl.obolibrary.org/obo/MONDO_0006459 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006459">
        <rdfs:label>thymoma type B1</rdfs:label>
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        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/predominantly_cortical_thymoma</ns4:curated_content_resource>
        <oboInOwl:hasExactSynonym>lymphocyte-rich thymoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C6887</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:6917</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0024418</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>organoid thymoma</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>A thymic epithelial neoplasm characterized by the presence of expanded areas which resemble the normal thymic cortex. The neoplastic epithelial cells are small and scant and there is a dense T-lymphocytic component present. Areas of medullary differentiation with or without Hassall&#39;s corpuscles are also present. It may be associated with myasthenia gravis, pure red cell aplasia, and hypogammaglobulinemia. It has a low grade malignant potential. The majority of cases occur in the anterior mediastinum as Masaoka stage I tumors. A minority of the cases occur as stage II tumors.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>predominantly cortical thymoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICDO:8583/1</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:1000584</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1266094</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>thymoma type B1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>lymphocyte-predominant thymoma</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>MEDGEN:224761</oboInOwl:hasDbXref>
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        <rdfs:label>thymoma type B</rdfs:label>
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