SE-ATLAS

Duchenne and Becker muscular dystrophy Limb-girdle muscular dystrophy Autosomal dominant limb-girdle muscular dystrophy Autosomal recessive limb-girdle muscular dystrophy Paramyotonia congenita of Von Eulenburg Duchenne muscular dystrophy Becker muscular dystrophy Myotonic dystrophy Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers Congenital myotonia Potassium-aggravated myotonia Myotonic syndrome Morvan syndrome Neuromuscular disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Amyotrophic lateral sclerosis Idiopathic camptocormia Genetic skeletal muscle disease Acquired skeletal muscle disease Infantile-onset ascending hereditary spastic paralysis Progressive muscular atrophy Juvenile primary lateral sclerosis Progressive muscular dystrophy Juvenile amyotrophic lateral sclerosis Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Non-dystrophic myopathy Proximal spinal muscular atrophy Macrophagic myofasciitis Muscular dystrophy-white matter spongiosis syndrome Distal myopathy Autosomal dominant proximal spinal muscular atrophy Poliomyelitis Thomsen and Becker disease Bulbospinal muscular atrophy Cyprus facial-neuromusculoskeletal syndrome Infantile-onset X-linked spinal muscular atrophy Intellectual disability-developmental delay-contractures syndrome Muscular tumor Infectious, fungal or parasitic myopathy Monomelic amyotrophy Myotonia fluctuans Neurogenic scapuloperoneal syndrome, Kaeser type Muscular dystrophy Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Isaacs syndrome Autosomal dominant childhood-onset proximal spinal muscular atrophy Amyotrophic lateral sclerosis type 4 Neuromuscular junction disease Genetic neuromuscular junction disease Motor neuron disease Acquired motor neuron disease Congenital muscular dystrophy Tel Hashomer camptodactyly syndrome Distal hereditary motor neuropathy Postpoliomyelitis syndrome Periodic paralysis Madras motor neuron disease Idiopathic dropped head syndrome Scapuloperoneal spinal muscular atrophy Myotonie permanente Myotonie sensible à l'acétazolamide Hyperthermie maligne de l'anesthésie Maladie du muscle squelettique Syndrome d'Andersen-Tawil Myopathie inflammatoire idiopathique Canalopathie musculaire Paralysie périodique avec pseudo-syndrome des loges transitoire Maladie acquise de la jonction neuromusculaire Maladie génétique du motoneurone Myopathie congénitale Dermatomyosite juvénile Paralysie périodique génétique