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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

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        <rdfs:label>syndromic intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010176 -->

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        <rdfs:label>orofaciodigital syndrome type 6</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/5588</ns5:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/4412/polydactyly-cleft-lip-palate-psychomotor-retardation</rdfs:seeAlso>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/orofaciodigital_syndrome_vi</ns3:curated_content_resource>
        <oboInOwl:hasExactSynonym>oral-facial-digital syndrome type 6</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>polydactyly cleft lip palate psychomotor retardation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:2754</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Varadi-Papp syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:277170</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Joubert syndrome with orofaciodigital defect</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Joubert syndrome with oral-facial-digital syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0004412</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:721873007</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>orofaciodigital syndrome VI</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Varadi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0010176</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>polydactyly - cleft lip/palate - psychomotor retardation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>DOID:0060376</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>orofaciodigital syndrome type 6</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:411200</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C124841</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536531</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>polydactyly-cleft lip/palate-psychomotor retardation syndrome</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>Joubert syndrome with orofaciodigital defect (or oral-facial-digital syndrome type 6, OFD6) is a very rare subtype of Joubert syndrome and related disorders (JSRD) characterized by the neurological features of JS associated with orofacial anomalies and often polydactyly.</ns5:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>Váradi syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Váradi-Papp syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C2745997</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>OFD6</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013824 -->

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        <rdfs:label>Joubert syndrome 17</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015375 -->

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        <rdfs:label>orofaciodigital syndrome</rdfs:label>
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