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    <!-- http://purl.obolibrary.org/obo/MONDO_0003266 -->

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        <rdfs:label>ependymal tumor</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016697 -->

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        <rdfs:label>low grade ependymoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016698 -->

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        <rdfs:label>ependymoma</rdfs:label>
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        <oboInOwl:hasNarrowSynonym>WHO grade II ependymal tumour</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasRelatedSynonym>ependymoma, familial</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>clear cell ependymoma (histologic variant)</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>DOID:4844</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006353</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>A WHO grade II, slow growing tumor of children and young adults, usually located intraventricularly. It is the most common ependymal neoplasm. It often causes clinical symptoms by blocking cerebrospinal fluid pathways. Key histological features include perivascular pseudorosettes and ependymal rosettes. (WHO)</ns5:IAO_0000115>
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        <oboInOwl:hasRelatedSynonym>tanycytic ependymoma (histologic variant)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0016698</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>papillary ependymoma (histologic variant)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasNarrowSynonym>WHO grade II ependymal neoplasm</oboInOwl:hasNarrowSynonym>
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        <oboInOwl:hasDbXref>MEDGEN:41825</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200088</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ependymoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:251636</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICDO:9391/3</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021639 -->

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        <rdfs:label>grade II glioma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024492 -->

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