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    <!-- http://purl.obolibrary.org/obo/MONDO_0013777 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0013777">
        <rdfs:label>pseudohypoaldosteronism type 2B</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019162"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/pseudohypoaldosteronism_type_iib_2</ns4:curated_content_resource>
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        <oboInOwl:hasDbXref>MEDGEN:374457</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>WNK4 pseudohypoaldosteronism type 2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>PHA2B</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the WNK4 gene.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>pseudohypoaldosteronism type 2 caused by mutation in WNK4</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0016776</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C564161</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>pseudohypoaldosteronism, type IIB</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0013777</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:88939</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:614491</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019162 -->

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        <rdfs:label>pseudohypoaldosteronism type 2</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_88939 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_88939">
        <rdfs:label>obsolete_pseudohypoaldosteronism type 2B</rdfs:label>
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