SE-ATLAS

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