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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_247775">
        <rdfs:label>obsolete_Classic Mayer-Rokitansky-Küster-Hauser syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Mayer-Rokitansky-Küster-Hauser syndrome type 1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:Q51.8</oboInOwl:hasDbXref>
        <ns5:obsoleted_in_version>3.41.0</ns5:obsoleted_in_version>
        <ns4:IAO_0000115>Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 1 is the classic type of MRKH syndrome (see this term) characterized by an isolated form of congenital aplasia of the uterus and upper two thirds of the vagina in otherwise phenotypically normal females.</ns4:IAO_0000115>
        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
        <ns5:definition_citation>orphanet</ns5:definition_citation>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0010173</ns4:IAO_0100001>
        <oboInOwl:hasExactSynonym>Rokitansky sequence</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Classic Rokitansky syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>MRKH syndrome type 1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:277000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Classic MRKH syndrome</oboInOwl:hasExactSynonym>
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