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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016965 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016965">
        <rdfs:label>partial duplication of the long arm of chromosome 15</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017806 -->

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        <rdfs:label>15q overgrowth syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>DECIPHER:81</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1661769</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>15q overgrowth syndrome is a rare partial autosomal trisomy/tetrasomy characterized by facial dysmorphism (long thin face, prominent forehead, down-slanting palpebral fissures, prominent nose with broad nasal bridge, prominent chin), pre- and postnatal overgrowth, renal anomalies (e.g. horseshoe kidney, renal agenesis, hydronephrosis), mild to severe learning difficulties and behavioral abnormalities. Additional features may include craniosynostosis and macrocephaly.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C4749920</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>15q26 overgrowth syndrome</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020226 -->

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