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    <!-- http://purl.obolibrary.org/obo/MONDO_0010959 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010959">
        <rdfs:label>van den Ende-Gupta syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015161"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015168"/>
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        <oboInOwl:hasDbXref>Orphanet:2460</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:719845008</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003382</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Marden Walker like syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Van den Ende Gupta syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C535909</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>van den Ende-Gupta syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Marden-Walker-like syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0111699</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>VDEGS</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>MEDGEN:322127</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Van den Ende-Gupta syndrome is a very rare syndrome characterized by blepharophimosis, arachnodactyly, joint contractures, and characteristic dysmorphic features.</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>Marden Walker like syndrome without psychomotor retardation</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015168 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015168">
        <rdfs:label>arthrogryposis multiplex congenita</rdfs:label>
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        <rdfs:label>obsolete_van den Ende-Gupta syndrome</rdfs:label>
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