SE-ATLAS

Progressive myoclonic epilepsy Adolescent-onset epilepsy syndrome Epilepsy syndrome Transient neonatal myasthenia gravis 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 Lambert-Eaton myasthenic syndrome Proximal spinal muscular atrophy Congenital myasthenic syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Hypnic headache PEHO-like syndrome Generalized epilepsy with febrile seizures-plus PEHO syndrome Rare epilepsy Autosomal dominant epilepsy with auditory features Moynahan syndrome Rare ataxia Muscular channelopathy Skeletal muscle disease 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 Motor neuron disease 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 Myasthenia gravis Benign focal seizures of adolescence Adult-onset myasthenia gravis Benign familial mesial temporal lobe epilepsy Neuromuscular disease Juvenile myasthenia gravis Chronic inflammatory demyelinating polyneuropathy