SE-ATLAS

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