SE-ATLAS

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 syndrome Morvan syndrome Skeletal muscle disease Genetic skeletal muscle disease Muscular dystrophy Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Acquired skeletal muscle disease Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Idiopathic inflammatory myopathy Oculopharyngodistal myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Autosomal dominant distal myopathy Tel Hashomer camptodactyly syndrome Non-dystrophic myopathy Genetic neuromuscular junction disease Lambert-Eaton myasthenic syndrome Acquired neuromuscular junction disease Autosomal recessive distal myopathy Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease 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 Neuromuscular disease Poliomyelitis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Infantile-onset ascending hereditary spastic paralysis Myotonic syndrome Potassium-aggravated myotonia Bulbospinal muscular atrophy Thomsen and Becker disease Proximal spinal muscular atrophy Periodic paralysis Rippling muscle disease with myasthenia gravis Muscular tumor Postpoliomyelitis syndrome Monomelic amyotrophy Infectious, fungal or parasitic myopathy Cyprus facial-neuromusculoskeletal syndrome Primary lateral sclerosis Idiopathic camptocormia