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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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        <rdfs:label>hypoproteinemia, hypercatabolic</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>immunodeficiency 43</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>Beta-2-microglobulin deficiency</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>GARD:0015185</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:343422</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0111981</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>B2M deficiency</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011476 -->

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