autoinflammatory syndrome
http://purl.obolibrary.org/obo/MONDO_0019751
A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. [ PMID:23827249 NCIT:C119050 ]
Term info
- Orphanet:93665 (MONDO:equivalentTo)
- NCIT:C119050 (MONDO:equivalentTo)
- UMLS:C3890737 (NCIT:C119050)
- MedDRA:10072220 (Orphanet:93665/e)
- ICD10CM:M04-M04 (https://orcid.org/0000-0002-4142-7153)
- UMLS:C3267073 (Orphanet:93665/e)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10072220
Editor note: todo - investigate diseases that have autoinflammatory and autommune components, e.g. IBD, Ankylosing Spondylitis, Axial Spondyloarthropathy, perhaps adult Onset Still's Disease. Consider disjointness axiom
A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease.
http://linkedlifedata.com/resource/umls/id/C3890737, http://purl.bioontology.org/ontology/ICD10CM/M04-M04, http://purl.obolibrary.org/obo/NCIT_C119050, http://linkedlifedata.com/resource/umls/id/C3267073, http://purl.obolibrary.org/obo/Orphanet_93665
MONDO:0019751