Adult-onset Still disease (AOSD) is a rare inflammatory multisystem disorder characterized clinically by fever of unknown origin, arthralgia or arthritis, hyperleucocytosis, and typical skin rash. [ Orphanet:829 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:759.89 (i2s)
  • MedDRA:10058493 (Orphanet:829)
  • ICD9:714.2 (i2s)
  • SCTID:239920006 (MONDO:equivalentTo)
  • DOID:14256 (MONDO:equivalentTo)
  • Orphanet:829 (MONDO:equivalentTo)
  • SCTID:68190001 (MONDO:equivalentTo)
  • UMLS:C0085253 (Orphanet:829)
  • MedDRA:10064056 (Orphanet:829)
  • EFO:0007135 (MONDO:equivalentTo)
  • MESH:D016706 (Orphanet:829)
  • UMLS:CN206037 (MONDO:equivalentTo)
  • ICD10:M06.1 (Orphanet:829)
  • GARD:0000436 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

abbreviation
AOSD [ Orphanet:829 ]

closeMatch

http://identifiers.org/snomedct/201815006

http://identifiers.org/snomedct/201449008

comment

Editor note: check if autoimmune

definition

Adult-onset Still disease (AOSD) is a rare inflammatory multisystem disorder characterized clinically by fever of unknown origin, arthralgia or arthritis, hyperleucocytosis, and typical skin rash.

exactMatch

http://identifiers.org/meddra/10058493

http://linkedlifedata.com/resource/umls/id/CN206037

http://purl.obolibrary.org/obo/DOID_14256

http://identifiers.org/meddra/10064056

http://linkedlifedata.com/resource/umls/id/C0085253

http://linkedlifedata.com/resource/umls/id/C0043195

http://www.orpha.net/ORDO/Orphanet_829

http://identifiers.org/snomedct/239920006

http://identifiers.org/mesh/D016706

http://identifiers.org/mesh/D014924

http://identifiers.org/snomedct/68190001

has exact synonym

AOSD

Wissler-Fanconi syndrome

adult-onset Still disease

adult-onset Still's disease

adult onset Still's disease

has related synonym

Still's disease adult onset

adult Still's disease

id

MONDO:0019355

seeAlso

https://rarediseases.info.nih.gov/diseases/436/adult-onset-stills-disease