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    <!-- http://purl.obolibrary.org/obo/MONDO_0005308 -->

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        <rdfs:label>ciliopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100451 -->

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        <rdfs:label>CEP290-related ciliopathy</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3898</ns3:IAO_0000233>
        <oboInOwl:hasNarrowSynonym>MKS4</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Meckel-like Cerebrorenodigital syndrome</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Meckel syndrome 4</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>CEP290 Senior-Loken syndrome</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>CEP290 Joubert syndrome</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>SLSN6</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>JBTS5</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Meckel syndrome, type 4</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>amaurosis congenita of Leber, type 10</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Joubert syndrome caused by mutation in CEP290</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasExactSynonym>CEP290 ciliopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>Leber congenital amaurosis type 10</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>SENIOR-Loken syndrome 6</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>GARD:0026225</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>CEP290 Meckel syndrome</oboInOwl:hasNarrowSynonym>
        <ns3:IAO_0000115>A ciliopathy caused by biallelic variants in the CEP290 gene.</ns3:IAO_0000115>
        <oboInOwl:hasNarrowSynonym>Joubert syndrome type 5</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Meckel syndrome caused by mutation in CEP290</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Senior-Loken syndrome caused by mutation in CEP290</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>CEP290 Leber congenital amaurosis</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Senior-Loken syndrome 6</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Senior-Loken syndrome type 6</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Leber congenital amaurosis caused by mutation in CEP290</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>LCA10</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Bardet-Biedl syndrome type 14</oboInOwl:hasNarrowSynonym>
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        <oboInOwl:hasNarrowSynonym>BBS14</oboInOwl:hasNarrowSynonym>
        <oboInOwl:id>MONDO:0100451</oboInOwl:id>
        <oboInOwl:hasNarrowSynonym>Leber congenital amaurosis 10</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Meckel-Gruber syndrome, type 4</oboInOwl:hasNarrowSynonym>
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