<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0010920"?>
<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#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#ordo_morphological_anomaly"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#closeMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010920 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010920">
        <rdfs:label>microtia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019755"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0024623"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/microtia_anotia</ns4:curated_content_resource>
        <oboInOwl:hasExactSynonym>microtia, congenital</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>microtias, congenital</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>congenital microtias</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10CM:Q17.2</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:35045004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:744.23</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:2005415414</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0010920</oboInOwl:id>
        <oboInOwl:hasDbXref>MESH:D065817</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>anotia</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>Orphanet:83463</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>microtia-anotia</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>A congenital malformation of the external ear, seen more frequently in males, that occurs sporadically or is inherited, that is characterized by unilateral (79-93% of cases, 60% of which involve the right ear) or bilateral small and abnormally shaped auricles and that is often associated with atresia or stenosis of the ear canal, attention deficit disorders and delayed language development. The variation in auricle size ranges from grade I, where the auricle is simply smaller than normal, to grade IV, also known as anotia, where there is a complete absence of the external ear and of the auditory canal.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0000431</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1833486</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:600674</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10027555</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537772</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>M-A</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:322201</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/2005415414"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10027555"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/322201"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D065817"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/35045004"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1833486"/>
        <skos:exactMatch rdf:resource="http://purl.bioontology.org/ontology/ICD10CM/Q17.2"/>
        <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#ordo_morphological_anomaly"/>
        <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_83463"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/600674"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019755 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019755">
        <rdfs:label>developmental defect during embryogenesis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0024623 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0024623">
        <rdfs:label>otorhinolaryngologic disease</rdfs:label>
    </Class>
</rdf:RDF>



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



