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    <!-- http://purl.obolibrary.org/obo/DOID_14447 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_14447">
        <rdfs:label xml:lang="en">gonadal dysgenesis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_3491 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_3491">
        <rdfs:label xml:lang="en">Turner syndrome</rdfs:label>
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        <oboInOwl:id>DOID:3491</oboInOwl:id>
        <oboInOwl:hasExactSynonym xml:lang="en">Gonadal dysgenesis - Turner</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS_CUI:C1527168</oboInOwl:hasDbXref>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasAlternativeId>DOID:5448</oboInOwl:hasAlternativeId>
        <oboInOwl:hasDbXref>NCI:C26900</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D014424</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2025_09_01:38804009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:2540</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCI:C34434</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:7831</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">Bonnevie-Ullrich syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS_CUI:C0041408</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:Q96</oboInOwl:hasDbXref>
        <ns3:IAO_0000115 xml:lang="en">A gonadal dysgenesis that is characterized by short stature and early loss of ovarian function resulting from ovarian hypofunction or premature ovarian failure and has_material_basis_in one missing or structurally altered X chromosome.</ns3:IAO_0000115>
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        <oboInOwl:hasExactSynonym xml:lang="en">Monosomy X</oboInOwl:hasExactSynonym>
        <rdfs:comment xml:lang="en">No OMIM mapping, confirmed by DO. [LS].</rdfs:comment>
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        <oboInOwl:hasExactSynonym xml:lang="en">monosomy X syndrome</oboInOwl:hasExactSynonym>
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