|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Benign essential blepharospasm from the curated CTD Gene-Disease Associations dataset.
|DRD5||dopamine receptor D5||2.88009|