| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D065635 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Benign Paroxysmal Positional Vertigo from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| BPPV | vestibulopathy, familial | 2.88009 |
