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    <!-- http://purl.obolibrary.org/obo/HP_0002196 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0002196">
        <rdfs:label>Myelopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0030709 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0030709">
        <rdfs:label>Myelocystocele</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0002196"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2016-02-25T21:32:46Z</dcterms:date>
        <oboInOwl:hasDbXref>UMLS:C0025312</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Myelocystocele is characterized by a large, ependyma-lined, cystic dilation of the caudal end of the central canal of the spinal cord; it projects dorsally through a lamina defect, with overlying varying amounts of lipomatous subcutaneous tissue. Myelocystoceles are associated with a tethered cord and meningocele, which communicates with the spinal subarachnoid space, but not with the central canal cyst.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>SNOMEDCT_US:414667000</oboInOwl:hasDbXref>
        <rdfs:comment>Localized dilatation of the central canal of the spinal cord which produces a fluid-filled sac or diverticulum which then protrudes through the cord and the defective dorsal dura between the posterior parts of the vertebra.</rdfs:comment>
        <oboInOwl:hasDbXref>SNOMEDCT_US:203994003</oboInOwl:hasDbXref>
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