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    <!-- http://purl.obolibrary.org/obo/MONDO_0003342 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003342">
        <rdfs:label>benign perivascular tumor</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016123 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016123">
        <rdfs:label>obsolete muscular tumor</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016824 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016824">
        <rdfs:label>infantile myofibromatosis</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0023603"/>
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        <oboInOwl:hasExactSynonym>myofibromatosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NORD:1301</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:140933</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>infantile myofibromatosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0432284</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0016824</oboInOwl:id>
        <oboInOwl:hasDbXref>ONCOTREE:IMS</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C3742</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:228550</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0080109</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0002998</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2591</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>IMS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>infantile hemangiopericytoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICDO:8824/1</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>multicentric myofibromatosis</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>A benign, multifocal, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma.</ns4:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019300 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019300">
        <rdfs:label>obsolete rare skin tumor or hamartoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0023603 -->

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        <rdfs:label>hereditary disorder of connective tissue</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0044335 -->

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        <rdfs:label>benign soft tissue neoplasm</rdfs:label>
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