| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Benign essential blepharospasm (BEB) is a cerebral focal and functional dystonia characterized by involuntary excessive blinking that can lead, in severe cases, to functional blindness due to the impossibility of re-opening the eyes at will. (Orphanet Rare Disease Ontology, Orphanet_93955) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C535428 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Benign essential blepharospasm from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| DRD5 | dopamine receptor D5 | 2.88009 |
