Term info
- UMLS:C0085253 (Orphanet:829/e)
- MESH:D016706 (Orphanet:829/e)
- UMLS:C0043195 (Orphanet:829/e)
- MedDRA:10064056 (Orphanet:829/e)
- ICD9:714.2 (MONDO:relatedTo)
- SCTID:239920006 (MONDO:equivalentTo)
- EFO:0007135 (MONDO:equivalentTo)
- UMLS:CN206037 (MONDO:equivalentTo)
- MESH:D014924 (Orphanet:829/e)
- Orphanet:829 (MONDO:equivalentTo)
- GARD:0000436 (MONDO:equivalentTo)
- SCTID:68190001 (MONDO:equivalentTo)
- DOID:14256 (MONDO:equivalentTo)
- MedDRA:10058493 (Orphanet:829/e)
- ICD9:759.89 (MONDO:relatedTo)
gard_rare, ordo_disease
http://identifiers.org/meddra/10058493, http://identifiers.org/meddra/10064056
A rare inflammatory multisystem disorder characterized clinically by fever of unknown origin, arthralgia or arthritis, hyperleucocytosis, and typical skin rash.
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
http://purl.obolibrary.org/obo/MONDO_0019724, http://purl.obolibrary.org/obo/MONDO_0005554
AOSD, Wissler-Fanconi syndrome, adult-onset Still's disease, adult-onset Still disease, adult onset Still's disease
Still's disease adult onset, adult Still's disease
MONDO:0019355
https://rarediseases.info.nih.gov/diseases/436/adult-onset-stills-disease