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    <!-- http://purl.obolibrary.org/obo/MONDO_0007671 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007671">
        <rdfs:label>fibronectin glomerulopathy</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100191"/>
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        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/glomerulopathy_with_fibronectin_deposits_2</ns4:curated_content_resource>
        <oboInOwl:hasExactSynonym>GFND</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>GFND2</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>GFND1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>fibronectin glomerulopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>glomerulopathy with fibronectin deposits 2</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0015019</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:137950</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:84090</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536826</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C3888104</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life.</ns3:IAO_0000115>
        <rdfs:comment>Editor note: consider splitting out type 1, and also separate class for giant subtype</rdfs:comment>
        <oboInOwl:hasDbXref>MEDGEN:854773</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>glomerulopathy with giant fibrillar deposits</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>glomerulopathy with fibronectin deposits</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1877494378</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:236535001</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>glomerular nephritis, familial, with fibronectin deposits</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C562900</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007671</oboInOwl:id>
        <oboInOwl:hasDbXref>NANDO:2200133</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>glomerulopathy with fibronectin deposits 1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>lobular glomerulopathy, familial</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019722 -->

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        <rdfs:label>glomerular disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0100191 -->

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        <rdfs:label>inherited kidney disorder</rdfs:label>
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