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        <rdfs:label>has_disease_location</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0004994 -->

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        <rdfs:label>cardiomyopathy</rdfs:label>
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        <rdfs:label>myocardium</rdfs:label>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_139027">
        <rdfs:label>Malformation syndrome with skin/mucosae involvement</rdfs:label>
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        <rdfs:label>Malformation syndrome with connective tissue involvement</rdfs:label>
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        <rdfs:label>Genetic dermis elastic tissue disorder</rdfs:label>
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        <rdfs:label>Pseudoxanthoma elasticum</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98054"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98056"/>
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        <oboInOwl:hasDbXref>OMIM:177850</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10037150</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0033847</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>PXE</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:264800</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Gronblad-Strandberg-Touraine syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:Q82.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D011561</oboInOwl:hasDbXref>
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        <rdfs:label>Rare genetic cardiac disease</rdfs:label>
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        <rdfs:label>Rare genetic renal disease</rdfs:label>
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        <rdfs:label>Connective tissue disease with eye involvement</rdfs:label>
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