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        <rdfs:label>obsolete_Costello syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Intellectual disability - nasal papillomata</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10067380</oboInOwl:hasDbXref>
        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
        <ns5:obsoleted_in_version>3.41.0</ns5:obsoleted_in_version>
        <oboInOwl:hasExactSynonym>FCS syndrome</oboInOwl:hasExactSynonym>
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        <ns5:definition_citation>orphanet</ns5:definition_citation>
        <oboInOwl:hasDbXref>UMLS:C0587248</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Faciocutaneoskeletal syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:218040</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Costello syndrome (CS) is a rare multisystemic disorder characterized by failure to thrive, short stature, developmental delay or intellectual disability, joint laxity, soft skin, and distinctive facial features. Cardiac and neurological involvement is common and there is an increased lifetime risk of certain tumors.</ns4:IAO_0000115>
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