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    <!-- http://www.orpha.net/ORDO/Orphanet_183576 -->

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        <rdfs:label>Genetic branchial arch or oral-acral syndrome</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_269550 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_269550">
        <rdfs:label>Genetic non-syndromic central nervous system malformation</rdfs:label>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_330197">
        <rdfs:label>Genetic multiple congenital anomalies/dysmorphic syndrome - variable intellectual disability</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_570 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_570">
        <rdfs:label>Moebius syndrome</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_269550"/>
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        <oboInOwl:hasDbXref>OMIM:157900</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0853240</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Moebius syndrome is a very rare congenital cranial dysinnervation disorder characterized by complete or incomplete facial paralysis in association with bilateral palsy of the abducens nerve causing impairment of ocular abduction. The syndrome also includes various other congenital anomalies.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:D020331</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0221060</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10:Q87.0</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Möbius syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10030069</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Congenital facial diplegia</oboInOwl:hasExactSynonym>
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        <rdfs:label>Syndrome with a symptomatic strabismus</rdfs:label>
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        <rdfs:label>Oculomotor palsy</rdfs:label>
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