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    <!-- http://purl.obolibrary.org/obo/MONDO_0016349 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016349">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">congenital hydrocephalus</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016350 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016350">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">hydrocephalus-blue sclerae-nephropathy syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016349"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019721"/>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Daentl-Townsend-Siegel syndrome</oboInOwl:hasExactSynonym>
        <ns2:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Hydrocephalus-blue sclera-nephropathy syndrome is a rare, genetic, renal or urinary tract malformation syndrome characterized by nephrotic syndrome with focal segmental sclerosis associated with hydrocephalus, thin skin and blue sclerae. There have been no further descriptions in the literature since 1978.</ns2:IAO_0000115>
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        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MONDO:0016350</oboInOwl:id>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019721 -->

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