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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005510 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005510">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">hydronephrosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007741 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007741">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">congenital hydronephrosis</rdfs:label>
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        <ns2:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Congenital hydronephrosis is a renal urinary disease characterized by distension and dilation of the renal pelvis and calyces secondary to various congenital obstructive malformations of the kidneys and urinary tract that can evolve to renal atrophy.</ns2:IAO_0000115>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Editor note: TODO check relationship to OMIM:143400</rdfs:comment>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q62.0</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD9:753.29</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019720 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019720">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">non-syndromic renal or urinary tract malformation</rdfs:label>
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