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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008796 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008796">
        <rdfs:label>aniridia-renal agenesis-psychomotor retardation syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015159"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0024458"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5588</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6744</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6745</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6877</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/aniridia_partial_with_unilateral_renal_agenesis_and_psychomotor_retardation</ns2:curated_content_resource>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/aniridia_renal_agenesis_psychomotor_retardation_syndrome</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0000690</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0008796</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:206750</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>aniridia renal agenesis psychomotor retardation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:1064</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:347952</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C000598722</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Sommer-Rathbun-Battles syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Sommer Rathbun Battles syndrome</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>Aniridia - renal agenesis - psychomotor retardation is an extremely rare syndrome reported in two siblings of non consanguineous parents that is characterized by the association of ocular abnormalities (partial aniridia, congenital glaucoma, telecanthus) with frontal bossing, hypertelorism, unilateral renal agenesis and mild psychomotor delay. There have been no further descriptions in the literature since 1974.</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>aniridia partial with unilateral renal agenesis and psychomotor retardation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C1859782</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:733116005</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C000598722"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024458 -->

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        <rdfs:label>disorder of visual system</rdfs:label>
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