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    <!-- http://purl.obolibrary.org/obo/MONDO_0005164 -->

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        <rdfs:label>fibrosarcoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006272 -->

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        <rdfs:label>low grade fibromyxoid sarcoma</rdfs:label>
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        <oboInOwl:hasDbXref>ONCOTREE:LGFMS</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A low grade, late-metastasizing variant of fibrosarcoma characterized by alternating fibrous and myxoid areas and a whorling growth pattern. The neoplastic cells have a spindle morphology, and lack hyperchromasia or significant nuclear atypia. Approximately 40% of cases show the focal presence of collagen rosettes. A t(7;16)(q33;p11) translocation has been identified in the majority of cases, associated with the presence of FUS-CREB3L2 fusion protein. Rare cases carry the t(11;16)(p11;p11) translocation which is associated with the presence of the FUS-CREB3L1 fusion protein.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>UMLS:C1275282</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:404088004</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0006272</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0024355</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C45202</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>low grade fibromyxoid sarcoma</oboInOwl:hasExactSynonym>
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