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    <rdfs:label>Dent disease</rdfs:label>
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    <obo:hasDbXref>Orphanet:1652</obo:hasDbXref>
    <obo:hasDbXref>NORD:1040</obo:hasDbXref>
    <obo:hasDbXref>MESH:D057973</obo:hasDbXref>
    <obo:hasDbXref>DOID:0050699</obo:hasDbXref>
    <obo:hasDbXref>NCIT:C123260</obo:hasDbXref>
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    <obo:hasExactSynonym>X-linked recessive nephrolithiasis</obo:hasExactSynonym>
    <obo:hasExactSynonym>Dent syndrome</obo:hasExactSynonym>
    <obo:hasExactSynonym>low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis</obo:hasExactSynonym>
    <obo:hasExactSynonym>X-linked recessive hypercalciuric hypophosphatemic rickets</obo:hasExactSynonym>
    <obo:hasExactSynonym>X-linked recessive hypophosphatemic rickets</obo:hasExactSynonym>
    <obo:hasExactSynonym>renal Fanconi syndrome with nephrocalcinosis and renal stones</obo:hasExactSynonym>
    <obo:hasRelatedSynonym>Dents disease</obo:hasRelatedSynonym>
    <obo:id>MONDO:0015612</obo:id>
    <ns3:IAO_0000115>Dent disease is a rare genetic renal tubular disease characterized by manifestations of proximal tubule dysfunction.</ns3:IAO_0000115>
    <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/dent_disease</ns2:curated_content_resource>
    <obo:hasNarrowSynonym>Dent disease 1</obo:hasNarrowSynonym>
    <obo:hasNarrowSynonym>Dent disease 2</obo:hasNarrowSynonym>
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    <skos:exactMatch rdf:resource="&obo;NCIT_C123260" />
    <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS300009" />
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    <rdfs:label>rickets</rdfs:label>
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<rdf:Description rdf:about="&obo;MONDO_0006510">
    <rdfs:label>renal tubular transport disease</rdfs:label>
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    <rdfs:label>inherited renal tubular disease</rdfs:label>
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