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    <!-- http://purl.obolibrary.org/obo/MONDO_0020598 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020598">
        <rdfs:label>malabsorption syndrome</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_165655 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_165655">
        <rdfs:label>Genetic intestinal disease</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_35858 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_35858">
        <rdfs:label>Gräsbeck-Imerslund disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020598"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_165655"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_79171"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98056"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98396"/>
        <oboInOwl:hasExactSynonym>Selective cobalamin malabsorption with proteinuria</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:D51.1</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:261100</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Familial megaloblastic anemia</oboInOwl:hasExactSynonym>
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    <!-- http://www.orpha.net/ORDO/Orphanet_79171 -->

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        <rdfs:label>Disorder of cobalamin metabolism and transport</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_98056 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_98056">
        <rdfs:label>Rare genetic renal disease</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_98396 -->

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        <rdfs:label>Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder</rdfs:label>
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