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

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001967">
        <rdfs:label>gonadal dysgenesis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010765 -->

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        <rdfs:label>46,XY complete gonadal dysgenesis</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021147"/>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6876</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/46xy_sex_reversal</ns2:curated_content_resource>
        <oboInOwl:hasExactSynonym>46, XY CGD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:445380</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D006061</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>46, XY pure gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>46,XY gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>46,XY complete gonadal dysgenesis (46,XY CGD) is a disorder of sex development (DSD) associated with anomalies in gonadal development that result in the presence of female external and internal genitalia despite the 46,XY karyotype.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>46,XY SEX reversal</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>gonadal dysgenesis, XY female type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>46, XY complete gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>sex-reversing locus on X</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>46,XY CGD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0005068</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>testis-determining Factor, X-chromosomal</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>sex-reversing locus on X, formerly</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NCIT:C120198</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:14448</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>46 XY gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:95218005</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Swyer syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIMPS:400044</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>46,XY pure gonadal dysgenesis</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0010765</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:242</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1750</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2936694</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019520 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019520">
        <rdfs:label>obsolete syndromic lymphedema</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021147 -->

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        <rdfs:label>disorder of development or morphogenesis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024573 -->

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        <rdfs:label>familial hypertrophic cardiomyopathy</rdfs:label>
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