SE-ATLAS

Adenosine monophosphate deaminase deficiency Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency Amyotrophic lateral sclerosis Barth syndrome Becker muscular dystrophy Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome DNA2-related mitochondrial DNA deletion syndrome Dermatomyositis Distal hereditary motor neuropathy type 1 Distal hereditary motor neuropathy type 2 Distal hereditary motor neuropathy type 5 Distal hereditary motor neuropathy type 7 Distal spinal muscular atrophy type 3 Duchenne muscular dystrophy Facioscapulohumeral dystrophy Immune-mediated necrotizing myopathy Inclusion body myositis Isolated complex I deficiency Isolated succinate-CoQ reductase deficiency Kearns-Sayre syndrome MELAS MERRF Mitochondrial DNA-related progressive external ophthalmoplegia Mitochondrial myopathy Mitochondrial myopathy and sideroblastic anemia Mitochondrial myopathy-lactic acidosis-deafness syndrome Mitochondrial neurogastrointestinal encephalomyopathy Mitochondrial trifunctional protein deficiency Muscular dystrophy Myotonic dystrophy Poliomyelitis Polymyositis Proximal myotonic myopathy Proximal spinal muscular atrophy Proximal spinal muscular atrophy type 1 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Pyruvate dehydrogenase E3 deficiency Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome Spinal muscular atrophy with respiratory distress type 1 Steinert myotonic dystrophy