Aetiology AED aggravation Aicardi-goutieres Aicardi Syndrome Alcohol Alpers disease Alternating hemiplagia Angelman Syndrome Autisme Autoimmune behavioural and personality disorders Bilirubin encephalopathy Biotinidase deficiency Brain malformation (not specified) Carbohydrate-deficient glycoprotein Ceroid-lipofuscinosis Chromosomal (not specified) Congenital disorders Congenital muscular dystrophy Congenital perisylvian syndrome Degenerative disease (unknown cause) Dentato-rubral-pallidoluysian degeneration Down syndrome Dysembryoplastic neuroepithelial tumor Dysplasia (architectural) Dysplasia (cytoarchitectural) Dysplasia (taylor-type) Encephalitis Encephalitis (anti-NMDA receptor) Febrile prolonged convulsion Focal cortical dysplasia (type i) Focal cortical dysplasia (type ii) folate deficiency (cerebral) Fragile x syndrome Ganglioganglioma Gaucher disease GENETIC Genetic Disorder Genetic predisposition Gliosis GLUT-1 deficiency Glycine encephalopathy Glycosylation Haemorrhage (cerebral) Hamartoma (cerebellar) Hamartoma (hypothalamic) Hamartoma (not specified) Hashimoto's thyropditis Head trauma Hemimegalencephaly Heterotopia (focal) Heterotopias (diffuse) Heterotopias (nodular periventricular) Heterotopia (subcortical band) HHH syndrome (Hyperornithinaemia-Hyperammonaemia-Homocitrullinaemia) Hippocampal sclerosis Holoprosencephaly Hyperekplexia Hypocalcemia Hypoglycemia Hyponatremia Hypoxia (postnatal) Hypoxic-ischemic encephalopathy Idiopathic Immune disorder Inborn metabolism error (aminoacids) Inborn metabolism error (organic acids) Incontinentia pigmenti Infarct (cerebral) Infection (brain) Infection (fetal, cmv) Infection (perinatal) Infection (prenatal) Ito disease KCNQ2 mutation Lafora disease Leigh disease lesion (unknown nature) Limbic encephalitis Linear naevus syndrome Lissencephaly Melas Menkes disease Merrf Metabolic disorder (not specified) Mitochindrial disorder Neurocutaneous syndrome (not specified) Neurofibromatosis Non epileptic paroxysmal disorder Nonketotic hyperglycinaemia Not applicable OLANZAPINE-INDUCED SEIZURES Pachygyria Panic attack Parasitic brain lesion Perinatal event (sequelae) Phenylketonuria Polymicrogyria (bilateral parasagittal) Polymicrogyria (bilateral perisylvian) Polymicrogyria (diffuse unilateral) Polymicrogyria (focal) Porencephaly Progressive myoclonic epilepsy (not specified) Prolonged convulsive episode Pyridoxine dependency Rasmussen encephalitis Reflex epilepsy Rett syndrome Ring chromosome 20 Sandifer syndrome Schizencephaly Sleep deprivation Stroke Sturge-Weber symptomatic Syncope (cardiac) Syncope (vagal) SYNGAP1 gene mutation Toxics abuse Trisomy 4p Tuberous sclerosis Tumor (brain) Unknown Unverricht-lundborg disease Variable Vascular malformation Venous thrombosis VITAMIN B12 DEFICIENCY VNS Withdrawal seizures (toxic) X-linked inantile spasms

Phenomenology Absence (dialeptic) seizure Absence seizure (typical) Agitation Akinetic seizure Anoxic seizure Aphasia (postictal) Aphasic seizure APNOEA Astatic seizure Atonic seizure (drop attack) Aura (abdominal) Aura (auditory) Aura (autonomic) Aura (gustatory) Aura (olfactory) Aura (psychic) Aura (somatomotor) Aura (visual) AUTOMATISMS Automotor (distal, mouth or tongue) seizure Automotor seizure Autonomic seizure Autonomic symptoms Axial BEHAVIOR (ALTERED) Bilateral asymmetric Bilateral symmetric Blinking (unilateral ictal) Bradycardia Catatonia clonic (non epileptic) Clonic seizure Consciousness (alteration) Consciousness (loss) Cough syncope Couphing CRYING Dacrystic seizure DANCING DES inducing spitting DIZZINESS DROP ATTACKS dyskinesias (non epileptic) Dyspraxia Dystonia (ictal) Ear plugging Eeg ictal discharge (infraclinical) EPILEPSIA PARTIALIS CONTINUA Epilepsy EPILEPTIC NYSTAGMUS Eructation Eye deviation Face Facial distortion FEAR Focal seizure not otherwise specified Focal seizure with affective symptoms Gelastic seizure Generalized Genital automatisms Grimace HALLUCINATIONS (AUDITORY) Hallucinations (visual) Headache HEAD DEVIATION Hiccup Hypermotor Hyperventilation Hypomotor seizure Ictal spitting Ictal vocalizations Ictal vomiting Ictus emeticus Kissing (ictal) LANGUAGE IMPAIRMENT Left Lip smacking Motor seizure (complex) Motor seizure (simple) Myoclonic atonic seizure myoclonic (eyelids) Myoclonic seizure myoclonic tonic Myoclonus (negative) MYOCLONUS (NON-EPILEPTIC)  Neonatal seizure Nocturnal seizure NON CONVULSIVE STATUS Nonepileptic paroxysmal event Nosewiping NYSTAGMUS OCULOCLONIC SEIZURES Panic attack Paradoxical version Paroxysmal arousal onset PHOTOSENSITIVE Pilomotor seizure POSTICAL SIGNS Reflex seizures Retching (ictal) Right Shuddering side-to-side axial movement Singing Sleep myoclonus Spasm (epileptic) Speech apraxia Staring Startle response Status epilepticus (convulsive) Status epilepticus (non convulsive) Stridor Stuttering Subclinical seizure Surgical technique Swearing (ictal) TICS Todd's paralysis Tonic-clonic seizure Tonic posture Tonic seizure Tonic spasms Urinary urge (ictal) Versive seizure Versive seizure (contralateral) Versive seizure (ipsilateral) Vomiting (ictal)

Localization Central (bilateral) Central (left) Central motor Central (right) Central sensory Centro-temporal region Cingulate Gyrus Entorhinal cortex Extra temporal Focal Frontal Eye Field Frontal lobe (bilateral) Frontal lobe (left) Frontal lobe (right) Frontal prefrontal lateral Frontal prefrontal mesial Frontal prefrontal mesiolateral Frontal premotor lateral Frontal premotor mesial Frontal premotor mesiolateral Generalized Hemispheric Hypothalamus Insula Insula (left) Insula (right) Left frontotemporal region Left hemispheric Midline Lesion Multifocal Multilobar excluding temporal Multilobar including temporal non-dominant hemisphere Non dominant temporal lobe Not applicable Occipital Opercular Operculum (left) Operculum (Right) Orbitofrontal Posterior cortex (bilateral) Posterior cortex (left) Posterior cortex occipital Posterior cortex parietal Posterior cortex (right) Right Sensimotor Cortex Supplementary motor area Temporal Temporal lateral Temporal lobe (bilateral) Temporal lobe (left) Temporal lobe (right) Temporal mesial Temporal mesiolateral Unkown

Syndrome Autosomal-dominant epilepsy with auditory features (ADEAF) Autosomal-dominant nocturnal frontal lobe epilepsy (ADNFLE) Benign familial infantile epilepsy Benign familial neonatal epilepsy (BFNE) Benign focal epilepsy with affective symptoms (BFEAS) Benign infantile epilepsy Childhood absence epilepsy (CAE) Chromosome 22q11.2 deletion Dravet syndrome Early myoclonic encephalopathy Epilepsia partialis continua Epilepsy not classified Epilepsy of infancy with Migrating focal seizures Epilepsy with generalized tonic-clonic seizures alone Epilepsy with myoclonic absences Epilepsy with myoclonic astatic (atonic) seizures Epileptic encephalopathy not otherwise classified Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWSS) Epileptic spasms epileptic spasms without hypsarrhythmia Febrile seizure plus Febrile seizures Focal non-idiopathic frontal (FLE) Focal non-idiopathic (localization not specified) Focal non-idiopathic mesiotemporal (MTLE with or without HS) Focal non-idiopathic occipital Focal non-idiopathic parietal Focal non-idiopathic temporal (TLE) GELASTIC SEIZURES WITH HYPOTHALAMIC HAMARTOMA Hemiconvulsion-Hemiplegia-Epilepsy (HHE) Hypothalamic hamartoma related seizures Idiopathic generalized not specified Idiopathic generalized other Jeavons syndrome Juvenile absence epilepsy (JAE) Juvenile myoclonic epilepsy (JME) Landau-Kleffner syndrome (LKS) Late onset childhood occipital epilepsy (Gastaut type) Lennox-Gastaut syndrome Lenox-Gastaut Syndrome Myoclonic encephalopathy in nonprogressive disorders Myoclonic epilepsy in infancy Neonatal seizures NEUROPSYCHIATRIC DISEASE Non epileptic paroxysmal disorder Not applicable Ohtahara syndrome Panayiotopoulos syndrome Perioral myoclonia with absences Photosensitive epilepsy Progressive myoclonic epilepsies (PME) Rasmussen syndrome Reflex epilepsies Rolandic epilepsy (BECTS) Sleep related hypermotor epilepsy (SHE) SYMPTOMATIC UNKNOWN West syndrome

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