SE-ATLAS

Proximal spinal muscular atrophy Periodic paralysis 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 Muscular channelopathy Amyotrophic lateral sclerosis Isaacs syndrome Juvenile amyotrophic lateral sclerosis Morvan syndrome Muscular dystrophy Skeletal muscle disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Tel Hashomer camptodactyly syndrome Lambert-Eaton myasthenic syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy Genetic motor neuron disease Motor neuron disease Myotonia fluctuans Acquired motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens 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 Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Myotonic syndrome Bulbospinal muscular atrophy Potassium-aggravated myotonia Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease