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    <!-- http://purl.obolibrary.org/obo/MONDO_0010542 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010542">
        <rdfs:label>dilated cardiomyopathy 3B</rdfs:label>
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        <oboInOwl:hasExactSynonym>DMD dilated cardiomyopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>dilated cardiomyopathy 3B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:777148</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>CMD3B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>dilated cardiomyopathy caused by mutation in DMD</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>DOID:0060561</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C580047</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>dilated cardiomyopathy type 3B</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>DOID:0110461</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SCTID:702424003</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Any dilated cardiomyopathy in which the cause of the disease is a mutation in the DMD gene.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>ICD9:425.4</oboInOwl:hasDbXref>
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        <rdfs:label>neuromuscular disease caused by qualitative or quantitative defects of dystrophin</rdfs:label>
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        <rdfs:label>hereditary neurological disease</rdfs:label>
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        <rdfs:label>familial isolated dilated cardiomyopathy</rdfs:label>
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