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    <!-- http://www.orpha.net/ORDO/Orphanet_1064 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_1064">
        <rdfs:label>Aniridia - renal agenesis - psychomotor retardation</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_183539"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_183763"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98632"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98640"/>
        <oboInOwl:hasExactSynonym>Sommer-Rathbun-Battles syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1859782</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10:Q87.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536371</oboInOwl:hasDbXref>
        <ns3: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 (see these terms), telecanthus) with frontal bossing, hypertelorism, unilateral renal agenesis (see this term) and mild psychomotor delay. There have been no further descriptions in the literature since 1974.</ns3:IAO_0000115>
        <ns4:definition_citation>orphanet</ns4:definition_citation>
        <oboInOwl:hasDbXref>OMIM:206750</oboInOwl:hasDbXref>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_183539">
        <rdfs:label>Genetic renal or urinary tract malformation</rdfs:label>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_183763">
        <rdfs:label>Rare genetic intellectual disability with developmental anomaly</rdfs:label>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_98632">
        <rdfs:label>Glaucoma associated with neural crest cell migration anomaly</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_98640 -->

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        <rdfs:label>Rare cataract</rdfs:label>
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