Term info
- SCTID:73442001 (MONDO:equivalentTo)
- ICD9:695.12 (MONDO:i2s)
- MESH:D013262 (Orphanet:36426/e)
- ICD9:695.13 (MONDO:i2s)
- NCIT:C79484 (MONDO:equivalentTo)
- ICD9:695.15 (DOID:0050426)
- DOID:0050426 (MONDO:equivalentTo)
- Orphanet:36426 (OMIM:608579)
- OMIM:608579 (Orphanet:36426/ntbt)
- UMLS:C0038325 (Orphanet:36426/e)
- EFO:0004276 (MONDO:equivalentTo)
- ICD10CM:L51.1 (Orphanet:36426/ntbt)
- GARD:0007700 (MONDO:equivalentTo)
- MedDRA:10042033 (Orphanet:36426/e)
ordo_clinical_subtype
http://identifiers.org/meddra/10042033
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.
http://purl.obolibrary.org/obo/DOID_0050426, http://purl.bioontology.org/ontology/ICD10CM/L51.1, http://purl.obolibrary.org/obo/Orphanet_36426, http://purl.obolibrary.org/obo/NCIT_C79484, http://identifiers.org/snomedct/73442001, http://identifiers.org/mesh/D013262, https://omim.org/entry/608579, http://linkedlifedata.com/resource/umls/id/C0038325
http://purl.obolibrary.org/obo/MONDO_0005594
Dermatostomatitis, Stevens Johnson type, Stevens Johnson syndrome
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
MONDO:0018229