Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q213098> ?p ?o }
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- Q213098 subject Q7467724.
- Q213098 subject Q8795300.
- Q213098 abstract "Progeria (pronunciation: /proʊˈdʒɪəriə/) (Hutchinson–Gilford progeria syndrome, HGPS, progeria syndrome) is an extremely rare genetic disorder wherein symptoms resembling aspects of aging are manifested at a very early age. Progeria is one of several progeroid syndromes. The word progeria comes from the Greek words "pro" (πρό), meaning "before" or "premature", and "gēras" (γῆρας), meaning "old age". The disorder has a very low incidence rate, occurring in an estimated 1 per 8 million live births. Those born with progeria typically live to their mid teens to early twenties. It is a genetic condition that occurs as a new mutation, and is rarely inherited, as carriers usually do not live to reproduce. Although the term progeria applies strictly speaking to all diseases characterized by premature aging symptoms, and is often used as such, it is often applied specifically in reference to Hutchinson–Gilford progeria syndrome (HGPS).Scientists are particularly interested in progeria because it might reveal clues about the normal process of aging. Progeria was first described in 1886 by Jonathan Hutchinson. It was also described independently in 1897 by Hastings Gilford. The condition was later named Hutchinson–Gilford progeria syndrome.".
- Q213098 icd10 "E34.8(ILDSE34.840)".
- Q213098 icd9 "259.8".
- Q213098 meshId "D011371".
- Q213098 omim "176670".
- Q213098 thumbnail Hutchinson-Gilford_Progeria_Syndrome.png?width=300.
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- Q213098 wikiPageExternalLink progeria.
- Q213098 wikiPageExternalLink NBK1121.
- Q213098 wikiPageExternalLink www.progeria.ca.
- Q213098 wikiPageExternalLink www.progeriaresearch.org.
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