Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.

Synonyms: Adult progeria WS

This is just here as a test because I lose it

Term information

database cross reference
expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=902

hasDbXref

MedDRA:10049429

ICD-10:E34.8

OMIM:277700

MeSH:D014898

UMLS:C0043119

has age of onset

http://www.orpha.net/ORDO/Orphanet_409948

http://www.orpha.net/ORDO/Orphanet_409947

has inheritance

http://www.orpha.net/ORDO/Orphanet_409930

has point prevalence range

http://www.orpha.net/ORDO/Orphanet_409977

http://www.orpha.net/ORDO/Orphanet_409976

notation

ORPHA:902

part of

http://www.orpha.net/ORDO/Orphanet_363245

http://www.orpha.net/ORDO/Orphanet_79389

http://www.orpha.net/ORDO/Orphanet_139027

http://www.orpha.net/ORDO/Orphanet_522548

http://www.orpha.net/ORDO/Orphanet_139033

http://www.orpha.net/ORDO/Orphanet_222628

http://www.orpha.net/ORDO/Orphanet_183422

http://www.orpha.net/ORDO/Orphanet_98641

present in

http://www.orpha.net/ORDO/Orphanet_409992

http://www.orpha.net/ORDO/Orphanet_410102

http://www.orpha.net/ORDO/Orphanet_410225

http://www.orpha.net/ORDO/Orphanet_409984

Term relations