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    <!-- http://purl.obolibrary.org/obo/HP_0000486 -->

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        <rdfs:label>Strabismus</rdfs:label>
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        <rdfs:label>syndromic disease</rdfs:label>
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        <rdfs:label>obsolete neuro-ophthalmological disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015369 -->

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        <rdfs:label>Joubert syndrome and related disorders</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016364 -->

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        <rdfs:label>Joubert syndrome with ocular defect</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6744</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6745</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns5:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/10168/joubert-syndrome-with-ocular-anomalies</rdfs:seeAlso>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/joubert_syndrome_with_ocular_defect</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0010168</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>JBTS3</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>icd11.foundation:1358617785</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>JS-O</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Joubert syndrome 3</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:716998009</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Joubert syndrome with ocular anomalies</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:909607</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C4274118</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders (JSRD) characterized by the neurological features of JS associated with retinal dystrophy.</ns5:IAO_0000115>
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