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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-chr6q24-q25 -->

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        <rdfs:label>6q24-q25 (Human)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000761 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000761">
        <rdfs:label>syndrome caused by partial chromosomal deletion</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013025 -->

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        <rdfs:label>chromosome 6q24-q25 deletion syndrome</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>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns5:IAO_0000233>
        <ns6:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/chromosome_6q24_q25_deletion_syndrome</ns6:curated_content_resource>
        <oboInOwl:hasExactSynonym>chromosome 6q25-q25 deletion syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>chromosome 6q24-q25 deletion syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>deletion 6q25</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>chromosome 6q25 microdeletion syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0013025</oboInOwl:id>
        <oboInOwl:hasDbXref>DOID:0060424</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:719663005</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C36470</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:612863</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:461565</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>6q25 microdeletion syndrome is a recently described syndrome characterized by developmental delay, facial dysmorphism and hearing loss.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:251056</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003764</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C3150215</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Del(6)(q25)</oboInOwl:hasExactSynonym>
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        <rdfs:label>partial deletion of the long arm of chromosome 6</rdfs:label>
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