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    <!-- http://purl.obolibrary.org/obo/MONDO_0012144 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0012144">
        <rdfs:label>Waardenburg syndrome type 2D</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9602</ns3:IAO_0000233>
        <ns3:IAO_0000115>Any Waardenburg syndrome type 2 in which the cause of the disease is a mutation in the SNAI2 gene.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>MESH:C563839</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Waardenburg syndrome type 2 caused by mutation in SNAI2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:323102</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>WS2D</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:608890</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Waardenburg syndrome type IID</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1837203</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0110952</oboInOwl:hasDbXref>
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