Bruck syndrome
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Summary
Bruck syndrome is a rare disease[1]. It draws 155 Wikipedia views per month (rare disease category, ranking #225 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: syndrome[4], osteogenesis imperfecta[5]
- Health specialty: rheumatology[6]
- Genetic association: FKBP10[7], PLOD2[8]
- Exact match: http://purl.obolibrary.org/obo/DOID_0060231[9], http://identifiers.org/doid/DOID:0060231[10], http://www.orpha.net/ORDO/Orphanet_2771[11]
- On focus list of Wikimedia project: WikiProject Medicine[12]
Why It Matters
Bruck syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[13] It is known by 12 alternative names across languages and contexts.[14]