Benign essential blepharospasm Gene Set

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)
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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