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        <rdfs:label>obsolete_Goldenhar syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Oculoauriculovertebral dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Expanded spectrum of hemifacial microsomia</oboInOwl:hasExactSynonym>
        <ns5:obsoleted_in_version>3.41.0</ns5:obsoleted_in_version>
        <oboInOwl:hasExactSynonym>Facioauriculovertebral dysplasia</oboInOwl:hasExactSynonym>
        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
        <ns5:definition_citation>orphanet</ns5:definition_citation>
        <oboInOwl:hasExactSynonym>OAVS</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>OAV dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D006053</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:164210</oboInOwl:hasDbXref>
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        <ns4:IAO_0000115>Goldenhar syndrome (GS), also known as oculo-auriculo-vertebral dysplasia (OAV), is a rare developmental syndrome characterized by a classic triad of mandibular hypoplasia resulting in facial asymmetry, ear and/or eye malformations, and vertebral anomalies.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C0432130</oboInOwl:hasDbXref>
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