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    <!-- http://purl.obolibrary.org/obo/MONDO_0007179 -->

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        <rdfs:label>autoimmune disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017287 -->

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        <rdfs:label>immunoglobulin G4-related sclerosing disease</rdfs:label>
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        <oboInOwl:hasDbXref>NANDO:1200924</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>IgG4-positive multiorgan lymphoproliferative syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>immunoglobulin G4-related sclerosing disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0012521</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>IgG4-related sclerosing disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:596448</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:284264</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>hyper-IgG4 disease</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>systemic IgG4-related sclerosing syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C3203653</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>systemic IgG4-related plasmacytic syndrome</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115>A recently described mass-forming lesion that occurs in the pancreas, submandibular glands, lacrimal glands, lymph nodes, and hepatobiliary tract. It is characterized by the presence of marked tissue sclerosis and infiltration by numerous plasma cells. The plasma cells show immunohistochemical staining for IgG4 and the serum IgG4 levels are often increased.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>MEDGEN:473761</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0080356</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MedDRA:10071569</oboInOwl:hasDbXref>
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