SE-ATLAS

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