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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
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    <!-- 
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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
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     -->

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0001967 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001967">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">gonadal dysgenesis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015218 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015218">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic developmental defect of the eye</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015620 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015620">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic urogenital tract malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016999 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016999">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">X chromosome number anomaly</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017143 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017143">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">genetic infertility</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017975 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017975">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">sex chromosome disorder of sex development</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018402 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018402">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">female infertility due to gonadal dysgenesis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019499 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019499">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Turner syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0001967"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015218"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015620"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016999"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017143"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017975"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018402"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019721"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019852"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020165"/>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">45, X syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">45,X gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">45,X syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">45,X/46,XX syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">45,X0 syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">45X syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Bonnevie-Ullrich syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Bonnevie-Ulrich syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">COHD:4307885</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">DOID:3491</oboInOwl:hasDbXref>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Editor note: consider splitting BU syndrome</rdfs:comment>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GARD:0002458</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GARD:0002459</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GARD:0002540</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GARD:0007831</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.0</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.1</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.2</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.3</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.4</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:Q96.9</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD9:758.7</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MESH:D014424</oboInOwl:hasDbXref>
        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MONDO:0019499</oboInOwl:id>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MedDRA:10045181</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">NCIT:C26900</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Orphanet:881</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">SCTID:38804009</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Schereshevkii Turner syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Turner Varny syndrome</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Turner syndrome is a chromosomal disorder associated with the complete or partial absence of an X chromosome.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">UMLS:C0041408</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Ullrich-Turner syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">XO syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">chromosome X monosomy X</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">genital dwarfism</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">genital dwarfism, Turner type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">gonadal dysgenesis (45,X)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">gonadal dysgenesis - Turner</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">gonadal dysgenesis Turner type</oboInOwl:hasRelatedSynonym>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/2458/genital-dwarfism</rdfs:seeAlso>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/2540/gonadal-dysgenesis-turner-type</rdfs:seeAlso>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/7831/turner-syndrome</rdfs:seeAlso>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">karyotype 45, X</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">monosomy X</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">monosomy X syndrome</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/meddra/10045181"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D014424"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/snomedct/157020008"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/snomedct/205685008"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/snomedct/205691005"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/snomedct/254279009"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/snomedct/268299006"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/snomedct/268356004"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/38804009"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0041408"/>
        <skos:closeMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0242526"/>
        <skos:closeMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1527168"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_malformation_syndrome"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_3491"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020226"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C26900"/>
        <skos:closeMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C34434"/>
        <skos:closeMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C85210"/>
        <ns3:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/mondo.owl"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_881"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019721 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019721">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic renal or urinary tract malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019852 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019852">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">inherited primary ovarian failure</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020165 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020165">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic epicanthus</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020226 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020226">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">chromosomal anomaly with cataract</rdfs:label>
    </Class>
</rdf:RDF>



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



