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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007712 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007712">
        <rdfs:label>oculoauriculovertebral spectrum with radial defects</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015161"/>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6751</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6877</ns3:IAO_0000233>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/hemifacial_microsomia_with_radial_defects</ns4:curated_content_resource>
        <ns3:IAO_0000115>Oculoauriculovertebral spectrum (OAVS) with radial defects is a rare branchial arches and limb primordia development disorder characterized by variable degrees of uni- or bilateral craniofacial malformation and radial defects that result in extremely variable phenotypic manifestations. Characteristic features include low postnatal weight, short stature, vertebral defects, hearing loss, and facial dysmorphism (incl. facial asymmetry, external, middle, and inner ear malformations, orofacial clefts, and mandibular hypoplasia). These features are invariably associated with radial defects, such as preaxial polydactyly, thumb and/or radius hypoplasia/agenesis, or triphalangeal thumb. Cardiac, pulmonary, renal, and central nervous system involvement has also been reported.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:141400</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Moeschler Clarren syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0003653</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hemifacial microsomia-radial defects syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Moeschler-Clarren syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0220681</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2549</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:726722009</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007712</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:67392</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>microsomia hemifacial radial defects</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018234 -->

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        <rdfs:label>dysostosis</rdfs:label>
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