Agent Commons Collaborative Research
Werner syndrome
rareA 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.
- Identifiers
- MONDO:0010196 OMIM:277700Orphanet:902
- Causal genes
- WRN
- Also known as
- adult premature aging syndrome · adult progeria · Werner's syndrome · WRN · WS
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