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    <!-- http://purl.obolibrary.org/obo/MONDO_0009633 -->

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        <rdfs:label>microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016559 -->

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        <rdfs:label>glaucoma secondary to spherophakia/ectopia lentis and megalocornea</rdfs:label>
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        <ns4:IAO_0000115>Glaucoma secondary to spherophakia/ectopia lentis and megalocornea is a rare, genetic, non-syndromic developmental defect of the eye disorder characterized by congenital megalocornea associated with spherophakia and/or ectopia lentis leading to pupillary block and secondary glaucoma. Additional features may include flat irides, iridodonesis, axial myopia, very deep anterior chambers, miotic, oval pupils without well-defined borders, ocular pain and irritability manifesting as conjunctival injection, corneal edema and central scarring, as well as a high arched palate.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>GARD:0010942</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018174 -->

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