Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C563399
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Genes

1 genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FCMTE1 familial cortical myoclonic tremor with epilepsy 1 2.88009