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     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     xmlns:owl="http://www.w3.org/2002/07/owl#"
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    <!-- 
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    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/reason_for_obsolescence"/>
    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/obsoleted_in_version"/>
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    <!-- http://www.orpha.net/ORDO/Orphanet_2969 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_2969">
        <rdfs:label>obsolete_Proteus-like syndrome</rdfs:label>
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        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <oboInOwl:hasDbXref>SCTID:716862002</oboInOwl:hasDbXref>
        <ns5:obsoleted_in_version>3.41.0</ns5:obsoleted_in_version>
        <oboInOwl:hasRelatedSynonym>Proteus like syndrome mental retardation eye defect</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0012801</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2969</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Cohen-Hayden syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Proteus-like syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:Q87.3</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0004525</oboInOwl:hasDbXref>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0017571</ns4:IAO_0100001>
        <oboInOwl:hasRelatedSynonym>Proteus like syndrome intellectual disability eye defect</oboInOwl:hasRelatedSynonym>
        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
        <ns4:IAO_0000115>Proteus-like syndrome describes patients who do not meet the diagnostic criteria for Proteus syndrome but who share a multitude of characteristic clinical features of the disease.</ns4:IAO_0000115>
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