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    <!-- http://purl.obolibrary.org/obo/RO_0004019 -->

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        <rdfs:label>disease has basis in</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_0050177 -->

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        <rdfs:label xml:lang="en">monogenic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_0060648 -->

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        <rdfs:label xml:lang="en">anterior segment dysgenesis</rdfs:label>
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        <oboInOwl:hasAlternativeId>DOID:0060605</oboInOwl:hasAlternativeId>
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        <oboInOwl:hasDbXref>ORDO:88632</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:Q13.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MIM:PS107250</oboInOwl:hasDbXref>
        <ns4:IAO_0000115 xml:lang="en">An eye disease that is characterized by iris hypoplasia, an enlarged or reduced corneal diameter, corneal vascularization and opacity, posterior embryotoxon, corectopia, polycoria, an abnormal iridocorneal angle, ectopia lentis, and anterior synechiae between the iris and posterior corneal surface and is located_in the anterior segment of the eye.</ns4:IAO_0000115>
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        <oboInOwl:hasExactSynonym xml:lang="en">corneal opacification and other ocular anomalies</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">iridogoniodysgenesis syndrome</oboInOwl:hasExactSynonym>
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