<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0007523"?>
<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://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007523 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007523">
        <rdfs:label>Ehlers-Danlos syndrome, hypermobility type</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020066"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/ehlers_danlos_syndrome_hypermobility_type</ns4:curated_content_resource>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/hypermobile_ehlers_danlos_syndrome</ns4:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>hypermobile Ehlers-Danlos syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Ehlers-Danlos syndrome, type 3</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>EDS III</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:14757</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0268337</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007523</oboInOwl:id>
        <oboInOwl:hasDbXref>NANDO:1200647</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>EDSHMB</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Ehlers-Danlos syndrome type 3</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0002081</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2201257</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:285</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Ehlers-Danlos syndrome, hypermobility type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>hypermobile EDS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:130020</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536196</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Ehlers-Danlos syndrome, hypermobility type (HT-EDS) is the most frequent form of EDS, a group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>NCIT:C125698</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>EDS3 (formerly)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>hEDS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Ehlers-Danlos syndrome type 3 (formerly)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:75670</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:30652003</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>HT-EDS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Ehlers-Danlos syndrome, type III</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Ehlers-Danlos syndrome, hypermobile type</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/75670"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C536196"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/30652003"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0268337"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_14757"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C125698"/>
        <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#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_285"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/130020"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020066 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020066">
        <rdfs:label>Ehlers-Danlos syndrome</rdfs:label>
    </Class>
</rdf:RDF>



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



