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    <!-- http://purl.obolibrary.org/obo/RO_0004022 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004022">
        <rdfs:label>disease arises from feature</rdfs:label>
        <rdfs:label>disease has basis in feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005154 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005154">
        <rdfs:label>liver disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009061 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009061">
        <rdfs:label>cystic fibrosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_7770005 -->

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        <rdfs:label>cystic fibrosis-related liver disease</rdfs:label>
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        <oboInOwl:hasExactSynonym>CF-related liver disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>CFLD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>CF liver disease</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>A liver disorder that arises as a consequence of cystic fibrosis. Cystic fibrosis-related liver disease encompasses a spectrum of hepatobiliary abnormalities caused by CFTR dysfunction in cholangiocytes, including focal biliary cirrhosis, multilobular biliary cirrhosis, hepatic steatosis, and cholangiopathy. It is a significant cause of non-pulmonary morbidity and mortality in CF, affecting approximately 5-10% of CF patients.</ns4:IAO_0000115>
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