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    <!-- http://purl.obolibrary.org/obo/MONDO_0009480 -->

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        <rdfs:label>Joubert syndrome with oculorenal defect</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6744</ns4:IAO_0000233>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns4:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/9455/joubert-syndrome-with-oculorenal-anomalies</rdfs:seeAlso>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/arima_syndrome</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>SCTID:721862000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>JS type B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>coloboma, chorioretinal, with cerebellar vermis aplasia</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>Joubert syndrome 5</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Cerebellooculorenal syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>CORS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:243910</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>cerebro-oculo-hepato-renal syndrome</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>chorioretinal coloboma with cerebellar vermis aplasia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Arima syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0009455</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200662</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1855675</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Joubert syndrome with oculorenal defect is a rare subtype of Joubert syndrome and related disorders (JSRD) characterized by the neurological features of JS associated with both renal and ocular disease.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>Orphanet:2318</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:340930</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015369 -->

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