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    <!-- http://purl.obolibrary.org/obo/MONDO_0011057 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011057">
        <rdfs:label>cerebrovascular disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017410 -->

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        <rdfs:label>porencephaly</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020496 -->

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        <oboInOwl:hasDbXref>Orphanet:99810</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1867983</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>An instance of porencephaly that is caused by an inherited modification of the individual&#39;s genome.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>hereditary porencephaly</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>familial porencephalic white matter disease</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>DOID:0112313</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100545 -->

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        <rdfs:label>hereditary neurological disease</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_99810 -->

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        <rdfs:label>obsolete_familial porencephaly</rdfs:label>
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