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    <!-- http://www.orpha.net/ORDO/Orphanet_1069 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_1069">
        <rdfs:label>Aniridia - absent patella</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_108987"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98632"/>
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        <oboInOwl:hasDbXref>OMIM:106220</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Aniridia-absent patella is a syndrome described in three members of a family (a boy, his father, and his paternal grandmother) that is characterized by the association of aniridia with patella aplasia or hypoplasia (see these terms). The grandmother also had bilateral cataracts and glaucoma. There have been no further descriptions in the literature since 1975.</ns3:IAO_0000115>
        <ns4:definition_citation>orphanet</ns4:definition_citation>
        <oboInOwl:hasDbXref>ICD10:Q87.8</oboInOwl:hasDbXref>
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    <!-- http://www.orpha.net/ORDO/Orphanet_108987 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_108987">
        <rdfs:label>Syndromic developmental defect of the eye</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_98632 -->

    <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 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_98640">
        <rdfs:label>Rare cataract</rdfs:label>
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