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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005594 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005594">
        <rdfs:label>severe cutaneous adverse reaction</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018229 -->

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        <rdfs:label>Stevens-Johnson syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>ICD10CM:L51.1</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:695.13</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:695.12</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:20955</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0007700</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Stevens Johnson syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0050426</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2201006</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:73442001</oboInOwl:hasDbXref>
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        <ns4:IAO_0000115>Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis characterized by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>NCIT:C79484</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10042033</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200245</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100290</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Dermatostomatitis, Stevens Johnson type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:36426</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019810 -->

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        <rdfs:label>toxic epidermal necrolysis</rdfs:label>
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