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 Idiopathic camptocormia Morvan syndrome Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Neuromuscular disease Amyotrophic lateral sclerosis Genetic skeletal muscle disease Proximal spinal muscular atrophy Autosomal dominant proximal spinal muscular atrophy Infantile-onset X-linked spinal muscular atrophy Periodic paralysis Muscular tumor Infectious, fungal or parasitic myopathy Monomelic amyotrophy Neurogenic scapuloperoneal syndrome, Kaeser type Muscular dystrophy Skeletal muscle disease Isaacs syndrome Acquired motor neuron disease Tel Hashomer camptodactyly syndrome Intellectual disability-developmental delay-contractures syndrome Idiopathic dropped head syndrome Myotonia permanens Myotonia fluctuans Acetazolamide-responsive myotonia Periodic paralysis with transient compartment-like syndrome Juvenile dermatomyositis Distal hereditary motor neuropathy Macrophagic myofasciitis Distal myopathy Thomsen and Becker disease Cyprus facial-neuromusculoskeletal syndrome Madras motor neuron disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Andersen-Tawil syndrome Amyotrophic lateral sclerosis type 4 Genetic periodic paralysis Muscular dystrophy-white matter spongiosis syndrome Poliomyelitis Bulbospinal muscular atrophy Postpoliomyelitis syndrome Autosomal dominant childhood-onset proximal spinal muscular atrophy Congenital muscular dystrophy Congenital myopathy Progressive muscular atrophy Scapuloperoneal spinal muscular atrophy Idiopathic inflammatory myopathy Muscular channelopathy Neuromuscular junction disease Genetic neuromuscular junction disease Acquired neuromuscular junction disease Motor neuron disease Genetic motor neuron disease Infantile-onset ascending hereditary spastic paralysis Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Juvenile amyotrophic lateral sclerosis Acquired skeletal muscle disease Juvenile primary lateral sclerosis Progressive muscular dystrophy Non-dystrophic myopathy