Human genes for Werner syndrome
Werner syndrome [DOID:5688]
A syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8.
Synonyms: Werner syndrome, DOID:5688, Werner disease, Werner disorder, Werner syndromes ...
Linkouts: OMIM