Werner syndrome

Summary
Synonym
  • WS
  • Werner's syndrome
  • adult premature ageing syndrome
  • adult progeria
Definition
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.
Super Class
autosomal recessive disease progeroid syndrome
External Links
Disease Ontology
DOID:5688
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 28 of 28 in total
Gene ID Gene Symbol Description Source
9365 KL klotho
22925 PLA2R1 phospholipase A2 receptor 1
22933 SIRT2 sirtuin 2
51548 SIRT6 sirtuin 6
55556 ENOSF1 enolase superfamily member 1
79661 NEIL1 nei like DNA glycosylase 1
151056 PLB1 phospholipase B1
159371 SLC35G1 solute carrier family 35 member G1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024