<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0007379"?>
<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://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"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ncit_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#should_conform_to"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000763 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000763">
        <rdfs:label>epithelial and subepithelial corneal dystrophy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007379 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007379">
        <rdfs:label>Meesmann corneal dystrophy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000763"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020212"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/9688/meesmann-corneal-dystrophy</rdfs:seeAlso>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/corneal_dystrophy_meesmann_1</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>MEDGEN:83283</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Meesmann corneal dystrophy (MECD) is a rare form of superficial corneal dystrophy characterized by distinct tiny bubble-like, round-to-oval punctate bilateral opacities in the central corneal epithelium, and to a lesser extent in the peripheral cornea, with little impact on vision.</ns3:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>corneal dystrophy, juvenile epithelial of Meesmann</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:371.51</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>juvenile hereditary epithelial dystrophy of Meesmann</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Meesmann corneal epithelial dystrophy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:1674008</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:98954</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0339277</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>corneal dystrophy, Meesmann</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Meesmann corneal dystrophy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C84795</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Meesman dystrophy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>MECD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>juvenile epithelial of Meesmann corneal dystrophy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0009688</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0060451</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007379</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIMPS:122100</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D053559</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/83283"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D053559"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/1674008"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0339277"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0060451"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C84795"/>
        <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#ncit_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"/>
        <ns4:should_conform_to rdf:resource="http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_98954"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS122100"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020212 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020212">
        <rdfs:label>superficial corneal dystrophy</rdfs:label>
    </Class>
</rdf:RDF>



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



