Disease association ontology term - MONDO:0010196 - Werner syndrome
Term summary
- ID
- MONDO:0010196
- Name
- Werner syndrome
- Ontology or CV name
- Disease association
- Definition
- 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.
