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    <!-- http://purl.obolibrary.org/obo/DOID_0080578 -->

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        <rdfs:label xml:lang="en">digenic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_2729 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_2729">
        <rdfs:label xml:lang="en">dyskeratosis congenita</rdfs:label>
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        <oboInOwl:id>DOID:2729</oboInOwl:id>
        <oboInOwl:hasDbXref>MIM:PS127550</oboInOwl:hasDbXref>
        <ns2:IAO_0000115 xml:lang="en">A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer.</ns2:IAO_0000115>
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        <rdfs:comment xml:lang="en">Xref MGI. OMIM mapping by NeuroDevNet. [LS].</rdfs:comment>
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