Neonatal Period Electroclinical Syndrome is related to benign neonatal seizures and early infantile epileptic encephalopathy. An important gene associated with Neonatal Period Electroclinical Syndrome is KCNQ2 (Potassium Voltage-Gated Channel Subfamily Q Member 2), and among its related pathways/superpathways are Neuropathic Pain-Signaling in Dorsal Horn Neurons and Neuroscience. Related phenotypes are Increased shRNA abundance (Z-score > 2) and Resistant to vaccinia virus (VACV-A4L) infection