<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0010426"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:skos="http://www.w3.org/2004/02/skos/core#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns4="http://purl.obolibrary.org/obo/mondo#"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/"
     xmlns:ns3="http://purl.obolibrary.org/obo/">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000766 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000766">
        <rdfs:label>corneal endothelial dystrophy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010426">
        <rdfs:label>X-linked endothelial corneal dystrophy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000766"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020214"/>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns3:IAO_0000233>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/corneal_dystrophy_endothelial_x_linked</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0017339</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:718579008</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>XECD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C567587</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>endothelial corneal dystrophy, X-linked</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0010426</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:293621</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:300779</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>corneal dystrophy, endothelial, X-linked</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1842066261</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:413518</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2749049</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>corneal dystrophy, endothelial, X-linked, X-linked dominant</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>X-linked endothelial corneal dystrophy (XECD) is a rare subtype of posterior corneal dystrophy characterized by congenital ground glass corneal clouding or a diffuse corneal haze, and blurred vision in male patients.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>DOID:0060446</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1842066261"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/413518"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C567587"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/718579008"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C2749049"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0060446"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_293621"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/300779"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020214 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020214">
        <rdfs:label>posterior corneal dystrophy</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



