SE-ATLAS

Autosomal dominant proximal spinal muscular atrophy Genetic periodic paralysis Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Macrophagic myofasciitis Andersen-Tawil syndrome Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Infantile-onset X-linked spinal muscular atrophy Distal myopathy Infantile-onset ascending hereditary spastic paralysis Potassium-aggravated myotonia Myotonic syndrome Thomsen and Becker disease Periodic paralysis Proximal spinal muscular atrophy Bulbospinal muscular atrophy Postpoliomyelitis syndrome Rippling muscle disease with myasthenia gravis Monomelic amyotrophy Muscular tumor Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Amyotrophic lateral sclerosis type 4 Madras motor neuron disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Muscular dystrophy Skeletal muscle disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Hereditary spastic paraplegia Juvenile amyotrophic lateral sclerosis Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Non-dystrophic myopathy Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Myotonia permanens Myotonia fluctuans Acetazolamide-responsive myotonia Neurogenic scapuloperoneal syndrome, Kaeser type