SE-ATLAS

Progressive myoclonic epilepsy Adolescent-onset epilepsy syndrome Epilepsy syndrome Neurocutaneous syndrome with epilepsy Benign adult familial myoclonic epilepsy Familial temporal lobe epilepsy Chromosomal anomaly with epilepsy as a major feature Familial focal epilepsy with variable foci Hereditary ataxia Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Monogenic disease with epilepsy New-onset refractory status epilepticus Inflammatory and autoimmune disease with epilepsy Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Rare headache Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Hypnic headache PEHO-like syndrome Generalized epilepsy with febrile seizures-plus PEHO syndrome Autosomal dominant epilepsy with auditory features Moynahan syndrome Rare ataxia SUNCT syndrome Acquired peripheral neuropathy Reversible cerebral vasoconstriction syndrome Oculocerebrocutaneous syndrome Neuromuscular junction disease Cranial neuralgia Genetic peripheral neuropathy Rare peripheral neuropathy Familial or sporadic hemiplegic migraine Action myoclonus-renal failure syndrome DEND syndrome Paroxysmal hemicrania Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Generalized epilepsy-paroxysmal dyskinesia syndrome Juvenile absence epilepsy Acquired sensory ganglionopathy Familial partial epilepsy Neuralgic amyotrophy Reflex epilepsy Autosomal dominant nocturnal frontal lobe epilepsy Childhood absence epilepsy Benign familial neonatal epilepsy Trigeminal autonomic cephalalgia Benign focal seizures of adolescence Benign familial mesial temporal lobe epilepsy Chronic inflammatory demyelinating polyneuropathy Adult-onset myasthenia gravis Juvenile myasthenia gravis Myasthenia gravis Transient neonatal myasthenia gravis Rare epilepsy