DOID:5688 - Werner syndrome
Disease Ontology Definition: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: WS, Werner's syndrome, adult premature ageing syndrome, adult progeria
|OMIM:277700 - WERNER SYNDROME; WRN|
|MONDO:0010196 - Werner syndrome|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : lmna, wrn
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD