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        <rdfs:label>obsolete_Dent disease</rdfs:label>
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        <oboInOwl:hasDbXref>ICD10:N25.8</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Dent&#39;s disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0878681</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Dent disease 1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Dent syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>Dent disease 2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10069199</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>An X-linked, recessive disorder of the proximal renal tubules that presents during childhood, and is characterized by low-molecular weight proteinuria, hypercalciuria, hypophosphatemia rickets, nephrocalcinosis, nephrolithiasis, and progressive kidney failure.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>X-Linked Recessive Hypophosphatemic Rickets</oboInOwl:hasExactSynonym>
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        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
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        <oboInOwl:hasDbXref>OMIM:300555</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Dents Disease</oboInOwl:hasExactSynonym>
        <ns2:IAO_0000115>Dent disease is a rare genetic renal tubular disease characterized by manifestations of proximal tubule dysfunction.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>X-linked recessive nephrolithiasis</oboInOwl:hasExactSynonym>
        <ns5:definition_citation>orphanet</ns5:definition_citation>
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        <oboInOwl:hasDbXref>OMIM:310468</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:308990</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ORDO:Orphanet_1652</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MESH:C545036</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0050699</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:300009</oboInOwl:hasDbXref>
        <ns2:IAO_0000117>Gautier Koscielny</ns2:IAO_0000117>
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