<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0019490"?>
<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.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#hasNarrowSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#should_conform_to"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000992 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000992">
        <rdfs:label>heart conduction disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019490 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019490">
        <rdfs:label>progressive familial heart block</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000992"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_1010180"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/familial_progressive_cardiac_conduction_defect</ns4:curated_content_resource>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/progressive_familial_heart_block</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>DOID:0111073</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial Lenègre disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>familial progressive heart block</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0010005</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:113900</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:426.6</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:871</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>hereditary bundle branch defect</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>SCTID:93130009</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial Lev-Lenègre disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1762068981</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A hereditary cardiac conduction disorder that may progress to complete atrioventricular (AV) block. The disease is either asymptomatic or manifests as dyspnea, dizziness, syncope, abdominal pain, heart failure or sudden death.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:698249005</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019490</oboInOwl:id>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1762068981"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/698249005"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0111073"/>
        <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"/>
        <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_871"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS113900"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_1010180 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_1010180">
        <rdfs:label>cardiogenetic rhythm disorder</rdfs:label>
    </Class>
</rdf:RDF>



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



