Behavioral abnormality, Bilateral tonic-clonic seizure, Bilateral tonic-clonic seizure with focal onset, Continuous spike and waves during slow sleep, Delayed speech and language development, Depression, Diffuse cerebral atrophy, Drooling, Dysarthria, Dysesthesia, Dysphasia, EEG with centrotemporal focal spike waves, EEG with focal sharp waves, EEG with generalized epileptiform discharges, EEG with irregular generalized spike and wave complexes, EEG with multifocal slow activity, Epileptic spasm, Febrile seizure (within the age range of 3 months to 6 years), Focal hemifacial clonic seizure, Focal-onset seizure, Generalized tonic seizure, Global developmental delay, Hypoplasia of the corpus callosum, Hyporeflexia, Incomprehensible speech, Infantile axial hypotonia, Infantile muscular hypotonia, Intellectual disability, Intellectual disability, borderline, Intellectual disability, moderate, Intellectual disability, severe, Laryngospasm, Migraine, Myoclonus, Nasal speech, Nocturnal seizures, Paresthesia, Pes cavus, Poor head control, Primary microcephaly, Profound global developmental delay, Secondary microcephaly, Seizure, Short attention span, Short nose, Short stature, Sleep apnea, Small for gestational age, Spasticity, Specific learning disability, Speech apraxia, Speech articulation difficulties, Stereotypical hand wringing, obsolete Focal seizures, afebril, obsolete Mood changes

decreased exploration in new environment, decreased kindling response, decreased thermal nociceptive threshold, decreased vertical activity, impaired contextual conditioning behavior, impaired cued conditioning behavior, increased startle reflex, jumpy, nervous system phenotype, reduced NMDA-mediated synaptic currents, reduced long term potentiation