SE-ATLAS

Acetazolamide-responsive myotonia Acquired motor neuron disease Acquired neuromuscular junction disease Acquired skeletal muscle disease Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Andersen-Tawil syndrome Autosomal dominant adult-onset proximal spinal muscular atrophy Autosomal dominant childhood-onset proximal spinal muscular atrophy Autosomal dominant distal hereditary motor neuropathy Autosomal dominant proximal spinal muscular atrophy Autosomal recessive distal hereditary motor neuropathy Bulbospinal muscular atrophy Bulbospinal muscular atrophy of adult Bulbospinal muscular atrophy of childhood Congenital myasthenic syndrome Cyprus facial-neuromusculoskeletal syndrome Distal myopathy Generalized bulbospinal muscular atrophy Genetic motor neuron disease Genetic neuromuscular junction disease Genetic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic camptocormia Idiopathic inflammatory myopathy Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Infectious, fungal or parasitic myopathy Intellectual disability-developmental delay-contractures syndrome Isaacs syndrome Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Lambert-Eaton myasthenic syndrome Lower motor neuron syndrome with late-adult onset Macrophagic myofasciitis Madras motor neuron disease Malignant hyperthermia of anesthesia Monomelic amyotrophy Morvan syndrome Motor neuron disease Muscular channelopathy Muscular dystrophy Muscular dystrophy-white matter spongiosis syndrome Muscular tumor Myasthenia gravis Myotonia fluctuans Myotonia permanens Myotonic syndrome Neurogenic scapuloperoneal syndrome, Kaeser type Neuromuscular disease Neuromuscular junction disease Non-dystrophic myopathy Paramyotonia congenita of Von Eulenburg Periodic paralysis Poliomyelitis Postpoliomyelitis syndrome Potassium-aggravated myotonia Primary lateral sclerosis Proximal spinal muscular atrophy Proximal spinal muscular atrophy type 1 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Rippling muscle disease with myasthenia gravis Skeletal muscle disease Spinal muscular atrophy associated with central nervous system anomaly Tel Hashomer camptodactyly syndrome Thomsen and Becker disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates X-linked distal spinal muscular atrophy type 3