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    <!-- http://purl.obolibrary.org/obo/RO_0004030 -->

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        <rdfs:label>disease arises from structure</rdfs:label>
        <rdfs:label>disease arises from alteration in structure</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHR_9606-chr8p -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHR_9606-chr8p">
        <rdfs:label>8p (Human)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000762 -->

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        <rdfs:label>syndrome caused by partial chromosomal duplication</rdfs:label>
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    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016929">
        <rdfs:label>partial duplication of chromosome 8</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016945 -->

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        <rdfs:label>partial duplication of the short arm of chromosome 8</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3492</ns5:IAO_0000233>
        <ns6:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/partial_duplication_of_the_short_arm_of_chromosome_8</ns6:curated_content_resource>
        <oboInOwl:hasExactSynonym>partial duplication of chromosome 8p</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>partial duplication of the short arm of chromosome type 8</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1632060</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1325415519</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>8p trisomy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Duplication 8p</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>trisomy 8p</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>chromosome 8p duplication</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0016945</oboInOwl:id>
        <oboInOwl:hasExactSynonym>partial trisomy of the short arm of chromosome 8</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>Chromosome 8p duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the short arm (p) of chromosome 8. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 8p duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Most cases are not inherited, but people can pass the duplication on to their children. Treatment is based on the signs and symptoms present in each person.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:262758</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>partial trisomy 8p</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C4708597</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>8p duplication</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>partial trisomy of chromosome 8p</oboInOwl:hasExactSynonym>
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