SE-ATLAS

Acetazolamide-responsive myotonia 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 childhood-onset proximal spinal muscular atrophy Autosomal dominant limb-girdle muscular dystrophy Autosomal dominant proximal spinal muscular atrophy Autosomal recessive limb-girdle muscular dystrophy Becker muscular dystrophy Bulbospinal muscular atrophy Congenital muscular dystrophy Congenital myopathy Congenital myotonia Cyprus facial-neuromusculoskeletal syndrome Distal hereditary motor neuropathy Distal myopathy Duchenne and Becker muscular dystrophy Duchenne muscular dystrophy Genetic motor neuron disease Genetic neuromuscular junction disease Genetic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic camptocormia Idiopathic dropped head syndrome 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 dermatomyositis Juvenile primary lateral sclerosis Limb-girdle muscular dystrophy 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 Myotonia fluctuans Myotonia permanens Myotonic dystrophy Myotonic syndrome Neurogenic scapuloperoneal syndrome, Kaeser type Neuromuscular disease Neuromuscular junction disease Non-dystrophic myopathy Paramyotonia congenita of Von Eulenburg Periodic paralysis Periodic paralysis with transient compartment-like syndrome Poliomyelitis Postpoliomyelitis syndrome Potassium-aggravated myotonia Progressive muscular atrophy Progressive muscular dystrophy Proximal spinal muscular atrophy Scapuloperoneal spinal muscular atrophy Skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers Tel Hashomer camptodactyly syndrome Thomsen and Becker disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates