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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001071 -->

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        <rdfs:label>intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009022 -->

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        <rdfs:label>corpus callosum, agenesis of</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021129 -->

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        <rdfs:label>microphthalmia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0023013 -->

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        <rdfs:label>Duker-Weiss-Siber syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C2930993</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Duker Weiss Siber syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:419689</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0023013</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>microphthalmos, microencephaly, mental retardation, agenesis of the corpus callosum, hypospadius, and cryptorchidism</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>microphthalmos, microencephaly, intellectual disability, agenesis of the corpus callosum, hypospadius, and cryptorchidism</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C535719</oboInOwl:hasDbXref>
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