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. [ NCIT:C119050 http://www.ncbi.nlm.nih.gov/pubmed/23827249 ]
Term information
- MedDRA:10072220 (Orphanet:93665/e)
- NCIT:C119050 (MONDO:equivalentTo)
- ICD10CM:M04-M04 (https://orcid.org/0000-0002-4142-7153)
- UMLS:C3890737 (NCIT:C119050)
- GARD:19234 (Orphanet:93665)
- Orphanet:93665 (MONDO:equivalentTo)
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders
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
http://www.orpha.net/ORDO/Orphanet_93665
http://linkedlifedata.com/resource/umls/id/C3890737
http://purl.bioontology.org/ontology/ICD10CM/M04-M04
http://purl.obolibrary.org/obo/NCIT_C119050