|  Help  |  About  |  Contact Us

DO Term : Werner syndrome [DOID:5688] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A progeroid 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:
  • SNOMEDCT_US_2023_03_01:51626007,
  • OMIM:277700,
  • NCI:C3447,
  • UMLS_CUI:C0043119,
  • MESH:D014898,
  • GARD:7885,
  • ORDO:902,
  • adult progeria,
  • 277700,
  • adult premature ageing syndrome,
  • Werner's syndrome,
  • WS
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents