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autoinflammatory syndrome

Go to external page 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. [ NCIT:C119050 http://www.ncbi.nlm.nih.gov/pubmed/23827249 ]

This is just here as a test because I lose it

Term information

database cross reference
  • NANDO:2100156 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C119050 (MONDO:equivalentTo)
  • Orphanet:93665 (MONDO:equivalentTo)
  • MEDGEN:855741 (MONDO:equivalentTo)
  • GARD:19234 (MONDO:GARD)
  • MedDRA:10072220 (Orphanet:93665/e)
  • ICD10CM:M04-M04 (https://orcid.org/0000-0002-4142-7153)
  • UMLS:C3890737 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10072220

comment

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

exactMatch

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

http://identifiers.org/medgen/855741

id

MONDO:0019751

Term relations