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    <!-- http://www.orpha.net/ORDO/Orphanet_84 -->

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        <rdfs:label>obsolete_Fanconi anemia</rdfs:label>
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        <oboInOwl:hasDbXref>OMIM:600901</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>OMIM:227646</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:227645</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:610832</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10:D61.0</oboInOwl:hasDbXref>
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