Epilepsy, Benign Neonatal 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:D020936
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Genes

2 genes/proteins associated with the disease Epilepsy, Benign Neonatal from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
BFIS1 benign familial infantile convulsions 2.88009
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2 2.88009