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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/4827 -->

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        <rdfs:label>HBB</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013517 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0013517">
        <rdfs:label>beta-thalassemia HBB/LCRB</rdfs:label>
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        <oboInOwl:hasExactSynonym>thalassemia, beta</oboInOwl:hasExactSynonym>
        <rdfs:comment>OMIM has the gene LCRB implicated in this disease but this gene does not exist in HGNC. It does exist in NCBI gene (HBB-LCR NCBIgene:109580095).</rdfs:comment>
        <oboInOwl:hasDbXref>OMIM:613985</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCDO:0000251</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0024933</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Abnormal clinical manifestations of beta thalassemia that are as a result of the underlying genotype.</ns4:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019402 -->

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