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    <!-- http://www.ebi.ac.uk/efo/EFO_0009050 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0009050">
        <rdfs:label>Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_183530"/>
        <ns2:IAO_0000115>A rare autosomal dominant syndromic intellectual disability syndrome characterized by macrocephaly, seizures, umbilical hernia, and facial dysmorphic features including frontal bossing, midface hypoplasia, small chin, hypertelorism with downslanting palpebral fissures, depressed nasal bridge, smooth philtrum, and thin upper lip (Smith et al., 2013; Baynam et al., 2015).</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:457485</oboInOwl:hasDbXref>
        <ns2:IAO_0000117>Hannah McLaren</ns2:IAO_0000117>
        <oboInOwl:hasExactSynonym>MINDS syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Smith-Kingsmore syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:616638</oboInOwl:hasDbXref>
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        <rdfs:label>Rare genetic developmental defect during embryogenesis</rdfs:label>
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