obsolete_Werner syndrome true orphanet http://purl.obolibrary.org/obo/MONDO_0010196 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. Replaced with Mondo term. OMIM:277700 MedDRA:10049429 UMLS:C0043119 MESH:D014898 WS 3.41.0 ICD10:E34.8 Adult progeria