Werner Syndrome
Disease ID: disease_node_7969
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| Dbxref | GARD:7885, MESH:D014898, MIM:277700, NCI:C3447, ORDO:902, SNOMEDCT_US_2023_03_01:51626007, UMLS_CUI:C0043119 |
|---|---|
| Subclassof | DOID_0081332, DOID_0050737 |
| Data Source | DOID, MESH |
| Synonyms | WS, Werner's syndrome, adult premature ageing syndrome, adult progeria |
| Mesh Id | D014898 |
| Mesh Label | Werner Syndrome |
| Mesh Subclassof | D030342, D049914 |
| Doid Label | Werner syndrome |
| Doid 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. OMIM mapping confirmed by DO. [LS]. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_7969 |
| Doid Id | DOID_5688 |
| Label | Werner Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Progeroid Syndrome(ID:disease_node_19958) (Disease)