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    <!-- http://purl.obolibrary.org/obo/MONDO_0005021 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005021">
        <rdfs:label>dilated cardiomyopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005217 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005217">
        <rdfs:label>familial cardiomyopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016333 -->

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        <rdfs:label>familial dilated cardiomyopathy</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C0340427</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>idiopathic dilated cardiomyopathy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIMPS:115200</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>dilated cardiomyopathy, familial</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>DCM</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:90951</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.</ns3:IAO_0000115>
        <oboInOwl:id>MONDO:0016333</oboInOwl:id>
        <oboInOwl:hasExactSynonym>hereditary dilated cardiomyopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>hypokinetic dilated cardiomyopathy, familial</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0020525</oboInOwl:hasDbXref>
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        <rdfs:label>obsolete_familial dilated cardiomyopathy</rdfs:label>
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