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    <!-- http://purl.obolibrary.org/obo/MONDO_0015079 -->

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        <rdfs:label>multiple polyglandular tumor</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015356 -->

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        <rdfs:label>hereditary neoplastic syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017169 -->

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        <rdfs:label>multiple endocrine neoplasia</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9285</ns3:IAO_0000233>
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        <ns3:IAO_0000115>Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:46724008</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>men syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0021044</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D009377</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100148</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:276161</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>multiple endocrine adenomatosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:258.0</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICDO:8360/1</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0027662</oboInOwl:hasDbXref>
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