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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_morphological_anomaly"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <rdfs:label>has characteristic</rdfs:label>
        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005510 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005510">
        <rdfs:label>hydronephrosis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007741 -->

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        <rdfs:label>congenital hydronephrosis</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4069</ns5:IAO_0000233>
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        <oboInOwl:hasDbXref>Orphanet:2190</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>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.</ns5:IAO_0000115>
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        <oboInOwl:hasDbXref>NANDO:2200176</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007741</oboInOwl:id>
        <rdfs:comment>Editor note: TODO check relationship to OMIM:143400</rdfs:comment>
        <oboInOwl:hasDbXref>ICD10CM:Q62.0</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021140 -->

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        <rdfs:label>congenital</rdfs:label>
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