benign neonatal seizures Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A neonatal period electroclinical syndrome that is characterized by tonic-clonic seizures in newborns occurring within the first seven days of life and ceasing within the first 15 weeks of life and has_material_basis_in autosomal dominant inheritance of voltage-gated potassium channels or a chromosomal inversion. (Human Disease Ontology, DOID_14264)
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Genes

6 genes co-occuring with the disease benign neonatal seizures 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 1.95206
KCNA6 potassium channel, voltage gated shaker related subfamily A, member 6 1.71681
PRRT2 proline-rich transmembrane protein 2 1.46891
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2 1.43244
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1 1.21305
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3 1.11351