SE-ATLAS

Acquired motor neuron disease Acquired neuromuscular junction disease Acquired skeletal muscle disease Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Andersen-Tawil syndrome Autosomal dominant proximal spinal muscular atrophy Bulbospinal muscular atrophy Congenital myasthenic syndrome Cyprus facial-neuromusculoskeletal syndrome Distal myopathy Genetic motor neuron disease Genetic neuromuscular junction disease Genetic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic camptocormia Idiopathic inflammatory myopathy Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Infectious, fungal or parasitic myopathy Intellectual disability-developmental delay-contractures syndrome Isaacs syndrome Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Lambert-Eaton myasthenic syndrome Macrophagic myofasciitis Madras motor neuron disease Malignant hyperthermia of anesthesia Monomelic amyotrophy Morvan syndrome Motor neuron disease Muscular channelopathy Muscular dystrophy Muscular dystrophy-white matter spongiosis syndrome Muscular tumor Myasthenia gravis Myotonic syndrome Neurogenic scapuloperoneal syndrome, Kaeser type Neuromuscular disease Neuromuscular junction disease Non-dystrophic myopathy Paramyotonia congenita of Von Eulenburg Periodic paralysis Poliomyelitis Postpoliomyelitis syndrome Potassium-aggravated myotonia Primary lateral sclerosis Proximal spinal muscular atrophy Rippling muscle disease with myasthenia gravis Skeletal muscle disease Tel Hashomer camptodactyly syndrome Thomsen and Becker disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates