autoimmune lymphoproliferative syndrome
Human disease
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Summary
autoimmune lymphoproliferative syndrome is a rare disease[1]. It draws 269 Wikipedia views per month (rare disease category, ranking #216 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: lymphoproliferative disorders[4], type IV hypersensitivity[5]
- Symptoms and signs: hepatomegaly[6], splenomegaly[7], lymphadenopathy[8]
- ICD-9-CM: 279.41[9]
- NCI Thesaurus ID: C37864[10]
- Health specialty: immunology[11]
- Genetic association: FAS[12], FASLG[13], CASP10[14], CASP8[15], CTLA4[16], KRAS[17], NRAS[18], PRKCD[19]
- Age of onset: any age[20]
- Exact match: http://purl.obolibrary.org/obo/DOID_6688[21], http://identifiers.org/doid/DOID:6688[22], http://www.orpha.net/ORDO/Orphanet_3261[23]
- On focus list of Wikimedia project: WikiProject Medicine[24]
- P14914: D03261[25]
Why It Matters
autoimmune lymphoproliferative syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[26] It is known by 15 alternative names across languages and contexts.[27]