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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/14000 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0014152 -->

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        <rdfs:label>left ventricular noncompaction 8</rdfs:label>
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        <oboInOwl:hasExactSynonym>left ventricular noncompaction 8</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:615373</oboInOwl:hasDbXref>
        <rdfs:comment>This appears in the series 115200 because of an included entity.</rdfs:comment>
        <oboInOwl:hasDbXref>MEDGEN:815618</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>LVNC8</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>cardiomyopathy, dilated, 1Ll</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>familial isolated dilated cardiomyopathy caused by mutation in PRDM16</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>UMLS:C3809288</oboInOwl:hasDbXref>
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