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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_2053">
        <rdfs:label>obsolete_Freeman-Sheldon syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.w3.org/2002/07/owl#Thing"/>
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        <oboInOwl:hasExactSynonym>Craniocarpotarsal dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:Q87.0</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10073655</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:193700</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0265224</oboInOwl:hasDbXref>
        <ns5:obsoleted_in_version>3.88.0</ns5:obsoleted_in_version>
        <ns5:reason_for_obsolescence>Replaced by Mondo term MONDO_0008675, with which this term was previously merged. This term is an old static import into EFO and is therefore out of date. It is being obsoleted in EFO for preservation and tracking. This term should be considered obsolete in EFO only if it differs from the domain source. Replaced by: http://purl.obolibrary.org/obo/MONDO_0008675</ns5:reason_for_obsolescence>
        <oboInOwl:hasDbXref>OMIM:277720</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Craniocarpotarsal dystrophy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C535483</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Freeman-Sheldon syndrome (FSS) is a very rare, multiple congenital contractures syndrome characterized by a microstomia with a whistling appearance of the mouth, distinctive facies, club foot and joint contractures. FSS is the most severe form of distal arthrogryposis.</ns4:IAO_0000115>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0008675</ns4:IAO_0100001>
        <ns5:definition_citation>orphanet</ns5:definition_citation>
        <oboInOwl:hasExactSynonym>Distal arthrogryposis type 2A</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Whistling face syndrome</oboInOwl:hasExactSynonym>
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