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 Amyotrophe Lateralsklerose Ionenkanalkrankheit, muskuläre Isaacs-Syndrom Muskelatrophie, scapuloperoneale spinale Amyotrophe Lateralsklerose, juvenile Morvan-Syndrom Skelettmuskel-Krankheit Genetisch bedingte Krankheit der Skelettmuskeln Spinale Muskelatrophie-progressive Myoklonusepilepsie-Syndrom Muskeldystrophie Paralyse, hypokaliämische periodische Paralyse, hyperkaliämische periodische Paramyotonia congenita Eulenburg Neuropathie, distale hereditäre motorische Erworbene Krankheit der Skelettmuskeln Myopathie, idiopathische inflammatorische Maligne Hyperthermie Neuromuskuläre Übertragungsstörung Tel-Hashomer-Kamptodaktylie-Syndrom