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adult-onset Still disease

^ http://purl.obolibrary.org/obo/MONDO_0019355

A rare inflammatory multisystem disorder characterized clinically by fever of unknown origin, arthralgia or arthritis, hyperleucocytosis, and typical skin rash. [ Orphanet:829 ]

Term info

database cross reference
  • UMLS:CN206037 (MONDO:equivalentTo)
  • MESH:D014924 (Orphanet:829/e)
  • MedDRA:10064056 (Orphanet:829/e)
  • SCTID:68190001 (MONDO:equivalentTo)
  • EFO:0007135 (MONDO:equivalentTo)
  • DOID:14256 (MONDO:equivalentTo)
  • ICD9:759.89 (MONDO:relatedTo)
  • Orphanet:829 (MONDO:equivalentTo)
  • SCTID:239920006 (MONDO:equivalentTo)
  • MESH:D016706 (Orphanet:829/e)
  • UMLS:C0043195 (Orphanet:829/e)
  • ICD9:714.2 (MONDO:relatedTo)
  • UMLS:C0085253 (Orphanet:829/e)
  • MedDRA:10058493 (Orphanet:829/e)
  • GARD:0000436 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

abbreviation
AOSD [ Orphanet:829 ]

closeMatch

http://identifiers.org/meddra/10058493, http://identifiers.org/meddra/10064056

definition

A rare inflammatory multisystem disorder characterized clinically by fever of unknown origin, arthralgia or arthritis, hyperleucocytosis, and typical skin rash.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN206037, http://purl.obolibrary.org/obo/DOID_14256, http://linkedlifedata.com/resource/umls/id/C0085253, http://purl.obolibrary.org/obo/Orphanet_829, http://identifiers.org/snomedct/239920006, http://identifiers.org/mesh/D016706, http://identifiers.org/snomedct/68190001

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019724, http://purl.obolibrary.org/obo/MONDO_0005554

has exact synonym

AOSD, Wissler-Fanconi syndrome, adult-onset Still's disease, adult-onset Still 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