SE-ATLAS

Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Myotonia fluctuans 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 Juvenile primary lateral sclerosis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Potassium-aggravated myotonia Myotonic syndrome Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Periodic paralysis Proximal spinal muscular atrophy Bulbospinal muscular atrophy 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 Amyotrophic lateral sclerosis Muscular channelopathy Isaacs-Syndrom Morvan-Syndrom Amyotrophe Lateralsklerose, juvenile Skelettmuskel-Krankheit Muskeldystrophie Paralyse, hypokaliämische periodische Paralyse, hyperkaliämische periodische Paramyotonia congenita Eulenburg Genetisch bedingte Krankheit der Skelettmuskeln Myopathie, idiopathische inflammatorische Erworbene Krankheit der Skelettmuskeln Maligne Hyperthermie Neuromuskuläre Übertragungsstörung Tel-Hashomer-Kamptodaktylie-Syndrom Neuromuskuläre Übertragungsstörung, genetisch bedingte Lambert-Eaton-Myasthenie-Syndrom Neuromuskuläre Übertragungsstörung, erworbene Myopathie, nichtdystrophe