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    <!-- http://purl.obolibrary.org/obo/MONDO_0015439 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015439">
        <rdfs:label>ring chromosome 4</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700011"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700091"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/1339/ring-chromosome-4</rdfs:seeAlso>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/ring_chromosome_4</ns4:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>chromosome 4 ring</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NORD:1671</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:1447</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Ring chromosome type 4</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Ring chromosome 4 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including significant intrauterine and postnatal growth retardation, developmental delay, intellectual disability, microcephaly, and dysmorphic facial features. Some less frequent features are cleft lip and/or cleft palate, congenital cardiovascular, gastrointestinal and genitourinary system anomalies.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>r(4) syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:75571</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>R4</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0001339</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>rose cluster 4</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>syndrome r(4)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Ring 4</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0015439</oboInOwl:id>
        <oboInOwl:hasDbXref>SCTID:81678004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C121983</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537636</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0265407</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700011 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700011">
        <rdfs:label>chromosome 4 disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700091 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700091">
        <rdfs:label>ring chromosome disorder</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_1447 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_1447">
        <rdfs:label>obsolete_ring chromosome 4</rdfs:label>
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