SE-ATLAS

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