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    <!-- http://purl.obolibrary.org/obo/MONDO_0002616 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002616">
        <rdfs:label>mesenchymal cell neoplasm</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006330 -->

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        <rdfs:label>ossifying fibromyxoid tumor</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C1266128</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>OFMT</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:404076001</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ossifying fibromyxoid tumour (morphologic abnormality)</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0006330</oboInOwl:id>
        <oboInOwl:hasDbXref>ONCOTREE:OFMT</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:226846</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:2685</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A rare soft tissue tumor of uncertain lineage characterized by the presence of neoplastic spindle to round cells forming cords in a fibromyxoid stroma. The lesions are associated with the formation of metaplastic bone. Most patients present with painless subcutaneous masses. Recurrences have been reported in a minority of patients.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>ossifying fibromyxoid tumor (morphologic abnormality)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICDO:8842/0</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C6582</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0037745 -->

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        <rdfs:label>fibromyxoid tumor</rdfs:label>
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