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    <!-- http://purl.obolibrary.org/obo/GSSO_006997 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GSSO_006997">
        <rdfs:label xml:lang="en">Williams-Beuren syndrome</rdfs:label>
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        <ns2:P3201 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">http://purl.bioontology.org/ontology/MEDDRA/10049644</ns2:P3201>
        <ns2:P5806 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">http://purl.bioontology.org/ontology/SNOMEDCT/63247009</ns2:P5806>
        <ns2:P699 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">http://purl.obolibrary.org/obo/DOID_1928</ns2:P699>
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        <ns2:P4229>Q93.82</ns2:P4229>
        <ns4:IAO_0000115 xml:lang="en">A genetic condition that affects many parts of the body. Facial features frequently include a broad forehead, short nose and full cheeks, an appearance that has been described as &quot;elfin&quot;. Mild to moderate intellectual disability with particular problems with visual spatial tasks such as drawing and fewer problems with language are typical. Those affected often have an outgoing personality and interact readily with strangers. Problems with teeth, heart problems, especially supravalvular aortic stenosis, and periods of high blood calcium are common</ns4:IAO_0000115>
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