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    <!-- http://purl.obolibrary.org/obo/MONDO_0015761 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015761">
        <rdfs:label>trisomy 10p</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>10p duplication</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Duplication 10p</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>trisomy type 10p</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0015761</oboInOwl:id>
        <ns4:IAO_0000115>Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10.</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>10p trisomy</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>SCTID:717157006</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C4082793</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C538290</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>partial trisomy 10p</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:904688</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>chromosome 10p duplication</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:171929</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016947 -->

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        <rdfs:label>partial duplication of the short arm of chromosome 10</rdfs:label>
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