SE-ATLAS

Proximal spinal muscular atrophy type 2 Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Proximal spinal muscular atrophy type 4 Proximal spinal muscular atrophy type 3 Primary lateral sclerosis Idiopathic camptocormia Lower motor neuron syndrome with late-adult onset Spinal muscular atrophy associated with central nervous system anomaly Muscular dystrophy-white matter spongiosis syndrome Autosomal dominant childhood-onset proximal spinal muscular atrophy Autosomal dominant adult-onset proximal spinal muscular atrophy Amyotrophic lateral sclerosis type 4 Madras motor neuron disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Autosomal dominant distal hereditary motor neuropathy Amyotrophic lateral sclerosis Muscular channelopathy Autosomal recessive distal hereditary motor neuropathy Isaacs syndrome Morvan syndrome Proximal spinal muscular atrophy type 1 Skeletal muscle disease Hypokalemic periodic paralysis Muscular dystrophy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Genetic skeletal muscle disease Idiopathic inflammatory myopathy Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Tel Hashomer camptodactyly syndrome Lambert-Eaton myasthenic syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy X-linked distal spinal muscular atrophy type 3 Motor neuron disease Myotonia fluctuans Acquired motor neuron disease Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Neurogenic scapuloperoneal syndrome, Kaeser type Adult-onset myasthenia gravis Autosomal dominant proximal spinal muscular atrophy Myasthenia gravis Congenital myasthenic syndrome Intellectual disability-developmental delay-contractures syndrome Genetic periodic paralysis Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Juvenile myasthenia gravis Myopathie, distale Lateralsklerose, juvenile primäre Spinale Muskelatrophie, infantile, X-chromosomale Transiente neonatale Myasthenia gravis Hereditäre Spastische Paralyse, aufsteigende, des frühen Kindesalters Muskelatrophie, bulbospinale Myotonie, Kalium-sensitive Myotones Syndrom Myotonia congenita Typ Thomsen und Becker Spinale Muskelatrophie, proximale Muskelatrophie, bulbospinale, des Kindes Periodische Paralyse Muskeltumor Muskelatrophie, bulbospinale, des Erwachsenen Post-Poliomyelitis-Syndrom Rippling-Muskel-Krankheit mit Myasthenia gravis Muskelatrophie, bulbospinale generalisierte Amyotrophie, monomelische