SE-ATLAS

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