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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/15561 -->

    <Class rdf:about="http://identifiers.org/hgnc/15561">
        <rdfs:label>IL36RN</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005083 -->

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        <rdfs:label>psoriasis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013626 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0013626">
        <rdfs:label>psoriasis 14, pustular</rdfs:label>
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        </rdfs:subClassOf>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/2829</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4496</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9686</ns5:IAO_0000233>
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        <oboInOwl:hasDbXref>GARD:0017679</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:614204</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200452</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0080474</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>deficiency of IL-36R antagonist</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:696.1</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:404546</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>psoriasis caused by mutation in IL36RN</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>PSORS14</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0392439</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0013626</oboInOwl:id>
        <oboInOwl:hasExactSynonym>deficiency of the interleukin-36 receptor antagonist</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>deficiency of IL-36Ra</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>GPP</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>familial generalised pustular psoriasis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Interleukin 36 receptor antagonist deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>generalized pustular psoriasis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>IL36RN psoriasis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:1200244</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:163931</oboInOwl:hasDbXref>
        <oboInOwl:hasBroadSynonym>palmoplantar pustulosis</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasExactSynonym>acrodermatitis continua of Hallopeau</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>Any psoriasis in which the cause of the disease is a mutation in the IL36RN gene.</ns5:IAO_0000115>
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        <oboInOwl:hasDbXref>MEDGEN:581114</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SCTID:83839005</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019268 -->

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        <rdfs:label>epidermal disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019299 -->

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        <rdfs:label>obsolete unclassified genetic skin disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019751 -->

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        <rdfs:label>autoinflammatory syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0023603 -->

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        <rdfs:label>hereditary disorder of connective tissue</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100491 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100491">
        <rdfs:label>generalized pustular psoriasis</rdfs:label>
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