Stevens-Johnson Syndrome

Preferred Label : Stevens-Johnson Syndrome;

NCIt related terms : Stevens Johnson Syndrome;

NCIt definition : A systemic, serious, and life-threatening disorder characterized by lesions in the skin and mucous membranes that may lead to necrosis. The lesions may appear anywhere in the body but they occur more commonly in the palms, soles, dorsum of the hands, and extensor surfaces. The lesions are vesicular or necrotic in the center, surrounded by an erythematous zone and occupy less than 10% of the body surfaces. The appearance of the mucocutaneous lesions is preceded by an upper respiratory tract infection. It is an immune complex hypersensitivity reaction usually caused by drugs (e.g., sulfa, phenytoin, penicillin), viruses (e.g., herpes simplex, influenza, hepatitis), and malignancies (e.g., carcinoma and lymphoma).;

Alternative definition : CTCAE: A disorder characterized by less than 10% total body skin area separation of dermis. The syndrome is thought to be a hypersensitivity complex affecting the skin and the mucous membranes.; NICHD: Drug or microbial induced exanthem characterized by papular or target-like lesions that involve less than 10% of the skin surface and at least two mucous membranes associated with systemic symptoms and may result in variable areas of skin necrosis.;

Codes from synonyms : E13736;

Details

Origin ID

C79484;

UMLS CUI

C0038325;

Currated CISMeF NLP mapping
- Bullous erythema multiforme [ICD-10 Sub-category (who)]
- Erythema multiforme minor [ICD-9 code]
- STEVENS JOHNSON SYNDROME [WHO-ART Preferred Term]
- Stevens Johnson reaction [MedDRA LLT]
- Stevens Johnson syndrome [Disease (Nov.)]
- Stevens Johnson syndrome [MedDRA LLT]
- Stevens-Johnson syndrome [PASCAL descriptor]
- Stevens-Johnson syndrome [ICD-10 Sub-category]
- Stevens-Johnson syndrome [DO Concept]
- Stevens-Johnson syndrome [ICD-11 Subcategory]
- Stevens-Johnson syndrome [MedDRA Preferred Term]
- Stevens-Johnson syndrome [MeSH concept]
- Stevens-Johnson syndrome [ORDO Disease]
- Stevens-Johnson syndrome (disorder) [SNOMED CT concept]
- Syndrome Stevens-Johnson [MedDRA LLT]
- stevens-johnson syndrome [MeSH Descriptor]
- stevens-johnson syndrome [SNOMED Notion]
DO Cross reference
- Stevens-Johnson syndrome [DO Concept]
Has associated anatomic sites
- Integumentary System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bullous erythema multiforme [MedDRA LLT]
- Bullous erythema multiforme [ICD-10 Sub-category (who)]
- Erythema exsudativum multiforme [MedDRA LLT]
- Erythema exudativum multiforme [MedDRA LLT]
- Erythema multiforme exudativum [MedDRA LLT]
- Erythema multiforme major [MedDRA LLT]
- STEVENS JOHNSON SYNDROME [WHO-ART Preferred Term]
- Stevens Johnson reaction [MedDRA LLT]
- Stevens Johnson syndrome [MedDRA LLT]
- Stevens Johnson syndrome [Disease (Nov.)]
- Stevens-Johnson syndrome [ORDO Disease]
- Stevens-Johnson syndrome [MedDRA Preferred Term]
- Stevens-Johnson syndrome [ICD-9 code]
- Stevens-Johnson syndrome [ICD-10 Sub-category]
- Stevens-Johnson syndrome [PASCAL descriptor]
- Stevens-Johnson syndrome [DO Concept]
- Stevens-Johnson syndrome [ICD-11 Subcategory]
- Stevens-Johnson syndrome [MeSH concept]
- Stevens-Johnson syndrome (disorder) [SNOMED CT concept]
- Syndrome Stevens-Johnson [MedDRA LLT]
- stevens-johnson syndrome [SNOMED Notion]
- stevens-johnson syndrome [MeSH Descriptor]
concept_is_in_subset
- CTCAE Adverse Events Version 4.0 Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Adverse Events Terminology [NCIt concept]
- Pediatric Adverse Events Terminology Mapped to MedDRA [NCIt concept]
disease_has_finding
- Cutaneous Involvement [NCIt concept]
disease_has_primary_anatomic_site
- Skin [NCIt concept]

Keyword's position in hierarchy(ies) :

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