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adult-onset Still disease

Go to external page 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 ]

Synonyms: AOSD Adult-Onset Still's Disease Wissler-Fanconi syndrome adult-onset Still's disease adult-onset Still disease adult onset Still's disease

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:436 (MONDO:GARD)
  • Orphanet:829 (MONDO:equivalentTo)
  • MedDRA:10058493 (Orphanet:829/e)
  • DOID:14256 (MONDO:equivalentTo)
  • MESH:D016706 (Orphanet:829/e)
  • icd11.foundation:549009522 (Orphanet:829)
  • MESH:D014924 (Orphanet:829/e)
  • EFO:0007135 (MONDO:equivalentTo)
  • ICD9:714.2 (MONDO:relatedTo)
  • NANDO:1200282 (https://orcid.org/0000-0003-0011-764X)
  • MEDGEN:39007 (MONDO:equivalentTo)
  • NORD:737 (MONDO:NORD)
  • UMLS:C0085253 (MONDO:equivalentTo)
  • SCTID:239920006 (MONDO:equivalentTo)
  • SCTID:68190001 (MONDO:equivalentTo)
  • MedDRA:10064056 (Orphanet:829/e)
  • ICD9:759.89 (MONDO:relatedTo)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare

abbreviation
AOSD [ Orphanet:829 ]

closeMatch

http://identifiers.org/meddra/10058493

http://identifiers.org/meddra/10064056

exactMatch

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

http://identifiers.org/medgen/39007

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

http://identifiers.org/snomedct/239920006

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

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 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