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    <!-- http://purl.obolibrary.org/obo/MONDO_0016838 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016838">
        <rdfs:label>16q24.3 microdeletion syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016914"/>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3664</ns3:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/10935/16q243-microdeletion-syndrome</rdfs:seeAlso>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/16q243_microdeletion_syndrome</ns4:curated_content_resource>
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        <oboInOwl:hasDbXref>UMLS:C4304594</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>16q24.3 microdeletion syndrome is a recently described syndrome associated with variable developmental delay, facial dysmorphism, seizures and autistic spectrum disorder.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:719580004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:930263</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0010935</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:261250</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Del(16)(q24.3)</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016914 -->

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        <rdfs:label>partial deletion of the long arm of chromosome 16</rdfs:label>
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        <rdfs:label>obsolete_16q24.3 microdeletion syndrome</rdfs:label>
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