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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://www.orpha.net/ORDO/Orphanet_139027 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_139027">
        <rdfs:label>Malformation syndrome with skin/mucosae involvement</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_183426 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_183426">
        <rdfs:label>Genetic epidermal disorder</rdfs:label>
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        <rdfs:label>Genetic respiratory or mediastinal malformation</rdfs:label>
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        <rdfs:label>Genetic respiratory malformation</rdfs:label>
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        <rdfs:label>LOC syndrome</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_139027"/>
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        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_263676"/>
        <oboInOwl:hasExactSynonym>LOGIC syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>LOC syndrome is a subtype of junctional epidermolysis bullosa (JEB, see this term) characterized by an altered cry in the neonatal period and by aberrant production of granulation tissue in particular affecting the upper airway tract, conjunctiva and periungual/subungual sites.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>Laryngo-onycho-cutaneous syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Shabbir syndrome</oboInOwl:hasExactSynonym>
        <ns4:definition_citation>orphanet</ns4:definition_citation>
        <oboInOwl:hasDbXref>ICD10:Q81.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:245660</oboInOwl:hasDbXref>
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    <!-- http://www.orpha.net/ORDO/Orphanet_263676 -->

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        <rdfs:label>Hereditary epidermolysis bullosa associated with ocular features</rdfs:label>
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