SE-ATLAS

Immune-mediated necrotizing myopathy Proximal spinal muscular atrophy Periodic paralysis Overlap myositis Muscular tumor Postpoliomyelitis syndrome Monomelic amyotrophy Antisynthetase syndrome Cyprus facial-neuromusculoskeletal syndrome Dermatomyositis Infectious, fungal or parasitic myopathy Juvenile idiopathic inflammatory myopathy Focal myositis 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 Muscular channelopathy Amyotrophic lateral sclerosis Isaacs syndrome Juvenile amyotrophic lateral sclerosis Morvan syndrome Muscular dystrophy Skeletal muscle disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy Motor neuron disease Eosinophilic fasciitis Genetic motor neuron disease Acquired motor neuron disease Inflammatory myopathy with abundant macrophages Idiopathic eosinophilic myositis Genetic periodic paralysis Neurogenic scapuloperoneal syndrome, Kaeser type Myasthenia gravis Autosomal dominant proximal spinal muscular atrophy Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Polymyositis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Myotonic syndrome Bulbospinal muscular atrophy Inclusion body myositis Potassium-aggravated myotonia Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease