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    <!-- http://purl.obolibrary.org/obo/MONDO_0015925 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015925">
        <rdfs:label>interstitial lung disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_1010089 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_1010089">
        <rdfs:label>hypomyopathic dermatomyositis</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8118</ns4:IAO_0000233>
        <ns4:IAO_0000115>A clinically amyopathic dermatomyositis with no subjective symptoms of skeletal muscle weakness but objective findings of muscle involvement (elevated aldolase level).</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0027228</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:619606071</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>HDM</oboInOwl:hasExactSynonym>
        <rdfs:comment>Patients with CADM and its subtypes are at risk of having associated interstitial lung disease and internal malignancies. (PMID:39005210)</rdfs:comment>
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