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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/5154 -->

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        <rdfs:label>HPGD</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007343 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007343">
        <rdfs:label>isolated congenital digital clubbing</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6876</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/digital_clubbing_isolated_congenital</ns5:curated_content_resource>
        <oboInOwl:hasExactSynonym>isolated congenital acropachy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>digital clubbing, isolated congenital</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0017117</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0345408</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Isolated congenital digital clubbing is a rare genodermatosis disorder characterized by enlargement of the terminal segments of fingers and toes with thickened nails without any other abnormality.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>OMIM:119900</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:217059</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:576901</oboInOwl:hasDbXref>
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        <rdfs:label>inherited isolated nail anomaly</rdfs:label>
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