SE-ATLAS

Congenital myasthenic syndrome 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 Potassium-aggravated myotonia Bulbospinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Proximal spinal muscular atrophy Periodic paralysis Muscular tumor Postpoliomyelitis syndrome Monomelic amyotrophy Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Immune-mediated acquired neuromuscular junction disease Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Idiopathic dropped head syndrome Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Progressive muscular atrophy Muscular channelopathy Amyotrophic lateral sclerosis Isaacs syndrome Scapuloperoneal spinal muscular atrophy Juvenile amyotrophic lateral sclerosis Morvan syndrome Genetic skeletal muscle disease Muscular dystrophy Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Skeletal muscle disease Hyperkalemic periodic paralysis Distal hereditary motor neuropathy Acquired skeletal muscle disease Paramyotonia congenita of Von Eulenburg Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Genetic neuromuscular junction disease Tel Hashomer camptodactyly syndrome Acquired neuromuscular junction disease Non-dystrophic myopathy Motor neuron disease Krankheit der Vorderhornzellen, autosomal-dominant oder rezessive Myotonia permanens Myotonia fluctuans Motoneuronkrankheit, erworbene Myotonia congenita, Azetazolamidempfindliche Botulismus Neurogenes scapulo-peroneales Syndrom Typ Kaeser Periodische Paralyse mit transienten Kompartment-ähnlichem Syndrom Periodische Paralyse, genetisch bedingte Spinale Muskelatrophie, proximale, autosomal-dominante