A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis). [ NCIT:C2889 ]

Synonyms: autoimmune disease or disorder autoimmune disorder disease, autoimmune autoimmune disease

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:109100 (MONDO:equivalentTo)
  • SCTID:85828009 (MONDO:equivalentTo)
  • EFO:0005809 (MONDO:equivalentTo)
  • NCIT:C2889 (MONDO:equivalentTo)
  • MEDGEN:2135 (MONDO:equivalentTo)
  • ICD9:279.4 (MONDO:relatedTo)
  • MESH:D001327 (MONDO:equivalentTo)
  • DOID:417 (MONDO:equivalentTo)
  • ICD9:720 (DOID:417)
  • OBI:1110054 (MONDO:equivalentTo)
  • UMLS:C0004364 (MONDO:equivalentTo)
  • ICD9:279.49 (MONDO:relatedTo)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, harrisons_view_immune_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, clingen, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_immune_system_disorder, harrisons_view_member, matrix_txgnn_grouping

comment

Editor note: check OMIM

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/autoimmune.yaml

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0007179

exactMatch

http://purl.obolibrary.org/obo/DOID_417

http://purl.obolibrary.org/obo/NCIT_C2889

https://omim.org/entry/109100

http://identifiers.org/medgen/2135

http://identifiers.org/snomedct/85828009

http://www.ebi.ac.uk/efo/EFO_0005809

http://linkedlifedata.com/resource/umls/id/C0004364

http://identifiers.org/mesh/D001327

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0000605

has related synonym

autoimmune hypersensitivity disease

hypersensitivity reaction type II disease

id

MONDO:0007179