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    <!-- http://www.orpha.net/ORDO/Orphanet_238446 -->

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        <rdfs:label>obsolete_15q11q13 microduplication syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Trisomy 15q11q13</oboInOwl:hasExactSynonym>
        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
        <ns5:obsoleted_in_version>3.41.0</ns5:obsoleted_in_version>
        <oboInOwl:hasExactSynonym>15q11-q13 duplication syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:608636</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>15q11q13 duplication syndrome</oboInOwl:hasExactSynonym>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0012081</ns4:IAO_0100001>
        <oboInOwl:hasExactSynonym>15q11-q13 microduplication syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:Q92.3</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>The 15q11-q13 microduplication (dup15q11-q13) syndrome is characterized by neurobehavioral disorders, hypotonia, cognitive deficit, language delay and seizures. Prevalence is unknown.</ns4:IAO_0000115>
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