Blepharospasm Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks. (Human Disease Ontology, DOID_529)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001764
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Genes

7 genes/proteins associated with the disease Blepharospasm from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DRD5 dopamine receptor D5 2.88009
DRD2 dopamine receptor D2 1.6043
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.38384
DRD1 dopamine receptor D1 1.28333
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.19509
PRL prolactin 1.167
GRIA1 glutamate receptor, ionotropic, AMPA 1 1.02634