Stevens-Johnson syndrome
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. [ ]
Term info
Stevens-Johnson syndrome
- Dermatostomatitis, Stevens Johnson type
- Stevens Johnson syndrome
- Stevens-Johnson syndrome
ordo_clinical_subtype
http://identifiers.org/meddra/10042033
http://purl.obolibrary.org/obo/DOID_0050426, http://purl.obolibrary.org/obo/Orphanet_36426, http://identifiers.org/snomedct/73442001, http://purl.obolibrary.org/obo/NCIT_C79484, http://identifiers.org/mesh/D013262, https://omim.org/entry/608579, https://icd.codes/icd10cm/L51.1, http://linkedlifedata.com/resource/umls/id/C0038325
http://purl.obolibrary.org/obo/MONDO_0005594
true
severe cutaneous adverse reaction, susceptibility to, hypersensitivity syndrome, carbamazepine-induced, susceptibility to, Stevens-Johnson syndrome, susceptibility to, toxic Epidermal necrolysis, susceptibility to, erythema multiforme major
EFO:0004276
Dani Welter