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    <!-- http://purl.obolibrary.org/obo/MONDO_0011604 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011604">
        <rdfs:label>spondylo-ocular syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020247"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0800064"/>
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        <oboInOwl:hasRelatedSynonym>spondyloocular syndrome</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>Spondylo-ocular syndrome is a very rare association of spinal and ocular manifestations that is characterized by dense cataracts, and retinal detachment along with generalized osteoporosis and platyspondyly. Mild craniofacial dysphormism has been reported including short neck, large head and prominent eyebrows.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0016740</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:85194</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MEDGEN:900371</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020247 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020247">
        <rdfs:label>congenital vitreoretinal dysplasia</rdfs:label>
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        <rdfs:label>osteogenesis imperfecta and a reduction of bone mineral density.</rdfs:label>
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        <rdfs:label>obsolete_spondylo-ocular syndrome</rdfs:label>
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