progeria
genetic disorder that causes early aging
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progeria
Summary
progeria is a developmental defect during embryogenesis[1]. progeria has Wikipedia articles in 28 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- progeria's instance of is recorded as developmental defect during embryogenesis[3].
- progeria's instance of is recorded as rare disease[4].
- progeria's instance of is recorded as class of disease[5].
- progeria is a type of autosomal dominant disease[6].
- progeria is a type of progeroid syndrome[7].
- progeria is a type of disease[8].
- progeria is a type of malformation syndrome with skin/mucosae involvement[9].
- progeria is a type of primary osteolysis[10].
- progeria is a type of syndrome[11].
- progeria is a type of autosomal genetic disease[12].
- progeria's Commons category is recorded as Progeria[13].
- progeria's topic's main category is recorded as Category:Progeria[14].
- progeria's ICD-9-CM is recorded as 259.8[15].
- progeria's NCI Thesaurus ID is recorded as C34951[16].
- progeria's health specialty is recorded as endocrinology[17].
- progeria's genetic association is recorded as LMNA[18].
- progeria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3911[19].
- progeria's exact match is recorded as http://identifiers.org/doid/DOID:3911[20].
- progeria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_740[21].
- progeria's on focus list of Wikimedia project is recorded as WikiProject Medicine[22].
Why It Matters
progeria has Wikipedia articles in 28 language editions, a strong signal of global cultural recognition.[2] progeria is known by 61 alternative names across languages and contexts.[23]