benign familial neonatal epilepsy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

6 genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2 2.45694
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3 1.7159
PRRT2 proline-rich transmembrane protein 2 1.69905
STX1A syntaxin 1A (brain) 0.778613
SCN2A sodium channel, voltage gated, type II alpha subunit 0.74761
CRH corticotropin releasing hormone 0.396353