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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic 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>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015218 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015218">
        <rdfs:label>obsolete syndromic developmental defect of the eye</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015334 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015334">
        <rdfs:label>obsolete branchial arch or oral-acral syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015397 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015397">
        <rdfs:label>craniofacial microsomia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0007712"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021635"/>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6452</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9285</ns5:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/12074/oculo-auriculo-vertebral-spectrum</rdfs:seeAlso>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/craniofacial_microsomia_1</ns2:curated_content_resource>
        <oboInOwl:hasExactSynonym>oculoauriculovertebral spectrum</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>HFM</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:75554</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D006053</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:109393007</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>unilateral or bilateral and asymmetric otomandibular dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>otomandibular syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Goldenhar syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:367462009</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>OAV spectrum</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:141136</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:141132</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C84740</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>facioauriculovertebral dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Expanded spectrum of hemifacial microsomia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>oculo-auriculo-vertebral spectrum</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>OAVD</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIMPS:164210</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:2907</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0012074</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>oculo-auriculo-vertebral dysplasia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>OAV dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Goldenhar disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Expanded spectrum hemifacial microsomia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Laterofacial microsomia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0265240</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:374</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>first branchial arch syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>oculoauriculovertebral dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>oculoauriculovertebral syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>hemifacial microsomia</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0015397</oboInOwl:id>
        <oboInOwl:hasExactSynonym>OAVS</oboInOwl:hasExactSynonym>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D006053"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/109393007"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/367462009"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0265240"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_2907"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015218"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015334"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020157"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020205"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020215"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020237"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0043008"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <ns2:should_conform_to rdf:resource="http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_141132"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS164210"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020157 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020157">
        <rdfs:label>obsolete syndromic palpebral coloboma</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020205 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020205">
        <rdfs:label>obsolete bulbar conjunctival dermoid or conjunctival dermolipoma</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020215 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020215">
        <rdfs:label>obsolete syndromic corneal dystrophy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020237 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020237">
        <rdfs:label>obsolete lens shape anomaly</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021635 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021635">
        <rdfs:label>neurocristopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0043008 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0043008">
        <rdfs:label>obsolete genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
    </Class>
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