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     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns5="http://purl.obolibrary.org/obo/mondo#"
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004029">
        <rdfs:label>disease has feature</rdfs:label>
    </ObjectProperty>
    


    <!-- 
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    <!-- http://purl.obolibrary.org/obo/HP_0000486 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000486">
        <rdfs:label>Strabismus</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002098 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002098">
        <rdfs:label>facial nerve disorder</rdfs:label>
    </Class>
    


    <!-- 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_0002320 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002320">
        <rdfs:label>congenital nervous system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0008006 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008006">
        <rdfs:label>Moebius syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002098"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002320"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015083"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015160"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004029"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0000486"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/10220</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6751</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/moebius_syndrome</ns5:curated_content_resource>
        <oboInOwl:hasExactSynonym>Moebius syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:13501</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:157900</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>absence or underdevelopment of the 6th and 7th cranial nerves</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MedDRA:10030069</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200980</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:89444000</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0008006</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0008549</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>oromandibular-limb hypogenesis spectrum</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10027789</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>MBS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>congenital oculofacial paralysis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Moebius sequence</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D020331</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C84893</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:570</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200559</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Mobius syndrome</oboInOwl:hasExactSynonym>
        <rdfs:comment>This term&#39;s classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the &#39;musculoskeletal system disorder&#39; (MONDO:0002081) ontology branch (https://orcid.org/0000-0001-9310-0163)</rdfs:comment>
        <ns4:IAO_0000115>A very rare congenital cranial dysinnervation disorder characterized by unilateral or bilateral non progressive congenital facial palsy (VII cranial nerve) with impairments of ocular abduction (VI cranial nerve). It can also be associated with other cranial nerves palsies, orofacial anomalies and limb defects.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>NORD:1453</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>congenital facial diplegia syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:66357</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Moebius Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Möbius syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0221060</oboInOwl:hasDbXref>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10027789"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10030069"/>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D020331"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/89444000"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0221060"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_13501"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C84893"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ncit_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_570"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/157900"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015083 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015083">
        <rdfs:label>nuclear oculomotor paralysis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015160 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015160">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
    </Class>
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