SE-ATLAS

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