| Dataset | ClinVar Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_5688) |
| External Link | http://www.omim.org/entry/277700 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the Werner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| WRN | Werner syndrome, RecQ helicase-like |
