Werner syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Werner syndrome | 902 | WRN | Causal Pathogenic evidence from ClinVar | - | ClinVar |
| Werner Syndrome | C0043119 | WRN | Causal Pathogenic evidence from ClinVar | 8602509, 8641691, 8968742, 9012406, 9048918, 9225981, 10347997, 10440702, 10543396, 10628995, 10678659, 10757812, 15235603, 15888165, 16673358, 16786514, 18810497, 20443122, 21267443, 22188495, 22766507, 25182132, 25390333, 28338660 | ClinVar |
| Atypical Werner syndrome | 79474, C4275075 | LMNA | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 12927431, 19270485 | - |