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    <!-- http://purl.obolibrary.org/obo/DOID_1062 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_1062">
        <rdfs:label xml:lang="en">Fanconi syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>SNOMEDCT_US_2025_09_01:40488004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS_CUI:C0341703</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MIM:PS134600</oboInOwl:hasDbXref>
        <oboInOwl:id>DOID:1062</oboInOwl:id>
        <oboInOwl:hasDbXref>NCI:C3034</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2025_09_01:236468006</oboInOwl:hasDbXref>
        <oboInOwl:hasAlternativeId>DOID:5956</oboInOwl:hasAlternativeId>
        <oboInOwl:hasDbXref>NCI:C4377</oboInOwl:hasDbXref>
        <ns3:IAO_0000115 xml:lang="en">A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym xml:lang="en">Congenital Fanconi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">Fanconi-de Toni syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:9118</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D005198</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS_CUI:C0015624</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">adult Fanconi Anemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">adult Fanconi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasExactSynonym xml:lang="en">De Toni-Fanconi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">Fanconi-de-Toni syndrome</oboInOwl:hasExactSynonym>
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        <rdfs:comment xml:lang="en">Xref MGI. OMIM mapping confirmed by DO. [SN].</rdfs:comment>
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