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    <!-- http://purl.obolibrary.org/obo/HP_0033130 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0033130">
        <rdfs:label>Abnormal renal echogenicity</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0033131 -->

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        <rdfs:label>Renal medullary hyperechogenicity</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0033130"/>
        <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2020-09-09T12:57:19Z</dc:date>
        <oboInOwl:hasExactSynonym>Increased renal medullary echogenicity</oboInOwl:hasExactSynonym>
        <ns2:IAO_0000115>Increased echogenecity of the medullary region of the kidney.</ns2:IAO_0000115>
        <rdfs:comment>Increased echogenicity of the kidney parenchyma results from the increased presence of material that can reflect sound waves back, thus increasing its brightness on the ultrasonography image. Because fibrous tissue (e.g., glomerulosclerosis, interstitial fibrosis) increases echogenicity, CKD is typically associated with increased echogenicity. Inflammatory infiltrates may explain the increased echogenicity that occurs with acute interstitial nephritis and GN. Proteinaceous casts are thought to cause the increased echogenicity associated with acute tubular necrosis (ATN). Calcium deposits and stones are very echogenic; thus, medullary nephrocalcinosis is characterized by increased medullary echogenicity and a relatively normal-appearing cortex. Several renal diseases are associated with medullary nephrocalcinosis, including medullary sponge kidney, hyperparathyroidism, renal tubular acidosis, and vitamin D toxicity. Other kidney diseases that have been associated with a hyperechoic medulla include sickle cell disease and gout</rdfs:comment>
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