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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-chr20q13 -->

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        <rdfs:label>20q13 (Human)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011812 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011812">
        <rdfs:label>Duane-radial ray syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016863 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016863">
        <rdfs:label>Okihiro syndrome due to 20q13 microdeletion</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/3664</ns5:IAO_0000233>
        <oboInOwl:hasExactSynonym>Okihiro syndrome due to del(20)(q13)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Okihiro syndrome due to monosomy 20q13</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C5679682</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0020787</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0016863</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:261638</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Duane-radial ray syndrome due to monosomy 20q13</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1826026</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016918 -->

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        <rdfs:label>partial deletion of the long arm of chromosome 20</rdfs:label>
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