SE-ATLAS

Distal myopathy Postpoliomyelitis syndrome Amyotrophic lateral sclerosis type 4 Amyotrophic lateral sclerosis Juvenile amyotrophic lateral sclerosis Inclusion myopathy Distal myopathy with posterior leg and anterior hand involvement Central core disease Distal myopathy, Welander type Nemaline myopathy Inclusion body myositis Mitochondrial myopathy Autosomal dominant childhood-onset proximal spinal muscular atrophy Congenital myopathy with cores Autosomal dominant adult-onset proximal spinal muscular atrophy Myopathic Ehlers-Danlos syndrome Distal hereditary motor neuropathy type 1 Autosomal dominant limb-girdle muscular dystrophy type 1A Multiminicore myopathy Proximal myotonic myopathy Tibial muscular dystrophy Glycogen storage disease due to acid maltase deficiency Kennedy disease Glycogen storage disease with hypertrophic cardiomyopathy Distal hereditary motor neuropathy