SE-ATLAS

Periodic paralysis with transient compartment-like syndrome Cystic fibrosis Andersen-Tawil syndrome Neuromuscular disease Rare pancreatic disease Epilepsy syndrome Potassium-aggravated myotonia Neurocutaneous syndrome with epilepsy Thomsen and Becker disease Chromosomal anomaly with epilepsy as a major feature Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Monogenic disease with epilepsy Cerebral malformation with epilepsy Inflammatory and autoimmune disease with epilepsy Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Primary eosinophilic gastrointestinal disease Rare tumor of salivary glands Carcinoma of the ampulla of Vater Primary lateral sclerosis Infectious disease with epilepsy Progressive muscular atrophy Rare epilepsy Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Skeletal muscle disease Genetic skeletal muscle disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Acquired skeletal muscle disease Inherited digestive cancer-predisposing syndrome Neuromuscular junction disease NK-cell enteropathy Genetic neuromuscular junction disease Acquired neuromuscular junction disease Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Malignant hyperthermia of anesthesia