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    <!-- http://purl.obolibrary.org/obo/MONDO_0010033 -->

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        <rdfs:label>generalized peeling skin syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024548 -->

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        <rdfs:label>peeling skin syndrome 1</rdfs:label>
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        <oboInOwl:hasDbXref>GARD:0017259</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>generalized deciduous skin type B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0070520</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inflammatory peeling skin syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>CDSN peeling skin syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>peeling skin syndrome 1</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>generalised peeling skin syndrome type B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>peeling skin syndrome type B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>generalized peeling skin syndrome type B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>generalised deciduous skin type B</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0024548</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:263553</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Any peeling skin syndrome in which the cause of the disease is a mutation in the CDSN gene.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>OMIM:270300</oboInOwl:hasDbXref>
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