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://www.ncbi.nlm.nih.gov/pubmed/23827249 NCIT:C119050 ]
Term information
- NANDO:2100156 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:855741 (MONDO:equivalentTo)
- Orphanet:93665 (MONDO:equivalentTo)
- MedDRA:10072220 (Orphanet:93665/e)
- NCIT:C119050 (MONDO:equivalentTo)
- GARD:19234 (MONDO:GARD)
- UMLS:C3890737 (MONDO:equivalentTo)
- ICD10CM:M04-M04 (https://orcid.org/0000-0002-4142-7153)
matrix_llm__is_cancer_other, gard_rare, harrisons_view_connective_tissue_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_syndromic_disease, mondo_top_grouping_connective_tissue_disorder, ordo_group_of_disorders, mondo_top_grouping_syndromic_disease
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
http://identifiers.org/medgen/855741