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    <!-- http://purl.obolibrary.org/obo/MONDO_0006541 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006541">
        <rdfs:label>epidermolysis bullosa</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018747 -->

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        <oboInOwl:hasDbXref>Orphanet:46487</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:4313</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006360</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acquired epidermolysis bullosa</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>ICD9:695.19</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>EBA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>epidermolysis bullosa Aquisita</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>epidermolysis bullosa acquisita</oboInOwl:hasExactSynonym>
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        <ns4:IAO_0000115>Epidermolysis bullosa acquisita (EBA) is a subepidermal bullous dermatosis of autoimmune origin that was named as a result of its resemblance to hereditary forms of epidermolysis bullosa (HEB), most notably dystrophic HEB.</ns4:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019337 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0021141 -->

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