Stevens–Johnson syndrome
skin disease
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Summary
Stevens–Johnson syndrome is a designated intractable/rare disease[1]. It ranks in the top 10% of designated intractable rare disease entities by monthly Wikipedia readership (10,963 views/month).[2]
Key Facts
- Instance of: class of disease[3]
- Named after: Albert Mason Stevens[4], Frank Chambliss Johnson[5], Ernst Wilhelm Baader[6]
- Subclass of: skin disease[7], erythema[8], severe cutaneous adverse reactions[9], syndrome[10], disease[11]
- Commons category: Stevens–Johnson syndrome[12]
- External data available at URL: http://www.nanbyou.or.jp/entry/4073[13]
- ICD-9-CM: 695.13[14]
- NCI Thesaurus ID: C79484[15], C79777[16]
- Health specialty: dermatology[17]
- Genetic association: PSORS1C1[18], POU5F1[19]
- Exact match: http://purl.obolibrary.org/obo/DOID_0050426[20], http://identifiers.org/doid/DOID:0050426[21], http://www.orpha.net/ORDO/Orphanet_537[22]
- On focus list of Wikimedia project: WikiProject Medicine[23]
Why It Matters
Stevens–Johnson syndrome has Wikipedia articles in 23 language editions, a strong signal of global cultural recognition.[24] It is known by 66 alternative names across languages and contexts.[25]