SE-ATLAS

Non-dystrophic myopathy Genetic neuromuscular junction disease Acquired neuromuscular junction disease Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Myotonia fluctuans Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Botulism Genetic periodic paralysis Periodic paralysis with transient compartment-like syndrome Congenital myasthenic syndrome Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Neuromuscular disease Poliomyelitis 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 Infectious, fungal or parasitic myopathy Monomelic amyotrophy Cyprus facial-neuromusculoskeletal syndrome Immune-mediated acquired neuromuscular junction disease 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 Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Scapuloperoneal spinal muscular atrophy Morvan syndrome Juvenile amyotrophic lateral sclerosis Skeletal muscle disease Genetic skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Muscular dystrophy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Distal hereditary motor neuropathy Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome