progeria
genetic disorder that causes early aging
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Summary
progeria is a developmental defect during embryogenesis[1]. progeria ranks in the top 1% of developmental defect during embryogenesis entities by monthly Wikipedia readership (16,385 views/month).[2]
Key Facts
- Instance of: rare disease[3], class of disease[4]
- Subclass of: autosomal dominant disease[5], progeroid syndrome[6], disease[7], malformation syndrome with skin/mucosae involvement[8], primary osteolysis[9], syndrome[10], autosomal genetic disease[11]
- Commons category: Progeria[12]
- Topic's main category: Category:Progeria[13]
- ICD-9-CM: 259.8[14]
- NCI Thesaurus ID: C34951[15]
- Health specialty: endocrinology[16]
- Genetic association: LMNA[17]
- Exact match: http://purl.obolibrary.org/obo/DOID_3911[18], http://identifiers.org/doid/DOID:3911[19], http://www.orpha.net/ORDO/Orphanet_740[20]
- On focus list of Wikimedia project: WikiProject Medicine[21]
Why It Matters
progeria has Wikipedia articles in 28 language editions, a strong signal of global cultural recognition.[22] progeria is known by 75 alternative names across languages and contexts.[23]