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    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/reason_for_obsolescence"/>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0700020 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0700020">
        <rdfs:label>obsolete_Birt-Hogg-Dube syndrome</rdfs:label>
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        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <oboInOwl:hasDbXref>EFO:1001273</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Birt-Hogg-Dube syndrome</oboInOwl:hasExactSynonym>
        <ns5:obsoleted_in_version>3.88.0</ns5:obsoleted_in_version>
        <oboInOwl:hasDbXref>SCTID:110985001</oboInOwl:hasDbXref>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0800444</ns4:IAO_0100001>
        <ns4:IAO_0000115>Birt-Hogg-Dube (BHD) syndrome is characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. It is a rare clinicopathologic condition named after the three Canadian physicians who reported the syndrome in 1977.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>DOID:0050676</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>fibrofolliculomas with trichodiscomas and acrochordons</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0346010</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10067736</oboInOwl:hasDbXref>
        <rdfs:comment>Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.</rdfs:comment>
        <oboInOwl:hasDbXref>ICD9:704.8</oboInOwl:hasDbXref>
        <ns5:reason_for_obsolescence>Replaced by Mondo term MONDO_0800444, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0800444</ns5:reason_for_obsolescence>
        <oboInOwl:hasDbXref>OMIM:135150</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D058249</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:122</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C28244</oboInOwl:hasDbXref>
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