SE-ATLAS

Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Myotonia fluctuans Genetic periodic paralysis Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Potassium-aggravated myotonia Myotonic syndrome Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Periodic paralysis Proximal spinal muscular atrophy Bulbospinal muscular atrophy Muscular tumor Postpoliomyelitis syndrome Rippling muscle disease with myasthenia gravis Monomelic amyotrophy 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 Juvenile amyotrophic lateral sclerosis Skeletal muscle disease Muscular dystrophy Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Idiopathic inflammatory myopathy Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Lambert-Eaton myasthenic syndrome Acquired neuromuscular junction disease Non-dystrophic myopathy