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| General Information | |||
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| Term | Werner syndrome | ID (Ontology) | DOID:5688 (Human Disease) |
| 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. | ||
| Also Known As | "adult premature ageing syndrome" ; "adult progeria" ; "Werner's syndrome" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ syndrome | |__progeroid syndrome___________| Werner syndrome 10 rec. |
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| Is a |
autosomal recessive disease progeroid syndrome |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:7885 MESH:D014898 MIM:277700 NCI:C3447 ORDO:902 SNOMEDCT_US_2023_03_01:51626007 UMLS_CUI:C0043119 |
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