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    <!-- http://purl.obolibrary.org/obo/MONDO_0016844 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016844">
        <rdfs:label>trisomy 20p</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016938"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/trisomy_20p</ns4:curated_content_resource>
        <oboInOwl:hasExactSynonym>partial trisomy of the short arm of chromosome 20</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>partial duplication of the short arm of chromosome 20</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0005333</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2930888</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>20p duplication</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:261318</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>partial trisomy 20p</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0016844</oboInOwl:id>
        <oboInOwl:hasDbXref>ICD9:758.5</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>chromosome 20p duplication</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115>Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterized by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>partial duplication of chromosome 20p</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:111311004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:418939</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>partial trisomy of chromosome 20p</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>20p trisomy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C535371</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>dup(20p)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Duplication of 20p</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>trisomy 20p</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>trisomy type 20p</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Duplication 20p</oboInOwl:hasRelatedSynonym>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C535371"/>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_261318"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016938 -->

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        <rdfs:label>partial trisomy of chromosome 20</rdfs:label>
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