Stevens-Johnson syndrome
A variant of bullous erythema multiforme. It ranges from mild skin and mucous membrane lesions to a severe, sometimes fatal systemic disorder. Ocular symptoms include ulcerative conjunctivitis, keratitis, iritis, uveitis, and sometimes blindness. The cause of the disease is unknown.
Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis characterized by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area.
Also appears inpride
Exact Synonyms
Dermatostomatitis, Stevens Johnson type
Stevens Johnson syndrome
Stevens-Johnson syndrome
Related Synonyms
erythema multiforme major
hypersensitivity syndrome, carbamazepine-induced, susceptibility to
severe cutaneous adverse reaction, susceptibility to
Stevens-Johnson syndrome, susceptibility to
toxic Epidermal necrolysis, susceptibility to
class Information
excluded_subClassOf
gwas_trait
true
has close match
has exact match
- http://identifiers.org/mesh/D013262
- http://identifiers.org/medgen/20955
- http://identifiers.org/snomedct/73442001
- http://linkedlifedata.com/resource/umls/id/C0038325
- http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/450167795
- Stevens-Johnson Syndromencit
- Stevens-Johnson syndromedoid
- http://purl.bioontology.org/ontology/ICD10CM/L51.1
- http://www.ebi.ac.uk/efo/EFO_0004276
- Stevens-Johnson syndromeordo
- https://omim.org/entry/608579
has_dbxref
- Stevens-Johnson syndromedoid
- GARD:7700
- ICD10CM:L51.1
- icd11.foundation:450167795
- ICD9:695.13
- ICD9:695.12
- ICD9:695.15
- MedDRA:10042033
- MedDRA:10015218
- MEDGEN:20955
- MESH:D013262
- MeSH:D013262
- Stevens-Johnson syndromemondo
- NANDO:1200245
- NANDO:2100290
- NANDO:2201006
- NCIt:C79484
- Stevens-Johnson Syndromencit
- OMIM:608579
- Orphanet:36426
- SCTID:73442001
- SNOMEDCT:73442001
- UMLS:C0038325
in_subset
term editor
Dani Welter