SE-ATLAS

Centronuclear myopathy Polymyositis Adult-onset myasthenia gravis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Vocal cord and pharyngeal distal myopathy Alveolar rhabdomyosarcoma Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Transient neonatal myasthenia gravis GNE myopathy Muscular glycogenosis Distal myopathy, Welander type Juvenile myasthenia gravis Congenital myopathy, Paradas type Proximal myotonic myopathy Hereditary myopathy with early respiratory failure Tibial muscular dystrophy Myotonic syndrome Bethlem muscular dystrophy X-linked myopathy with excessive autophagy Potassium-aggravated myotonia Autosomal dominant spastic paraplegia type 17 Bulbospinal muscular atrophy of adult Muscular dystrophy, Selcen type Pontocerebellar hypoplasia type 1 Bulbospinal muscular atrophy of childhood Generalized bulbospinal muscular atrophy Antisynthetase syndrome Dermatomyositis Adult-onset distal myopathy due to VCP mutation Myosclerosis Fungal myositis Parasitic myositis Juvenile overlap myositis Autosomal dominant childhood-onset proximal spinal muscular atrophy Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Spheroid body myopathy Megaconial congenital muscular dystrophy Autosomal dominant distal hereditary motor neuropathy Fingerprint body myopathy Autosomal dominant congenital benign spinal muscular atrophy Rippling muscle disease O'Sullivan-McLeod syndrome Native American myopathy Distal hereditary motor neuropathy type 1 Juvenile amyotrophic lateral sclerosis Corpus callosum agenesis-neuronopathy syndrome Rigid spine syndrome Facioscapulohumeral dystrophy Distal myopathy with anterior tibial onset Hypokalemic periodic paralysis Infantile myofibromatosis Myxofibrosarcoma Steinert myotonic dystrophy Tubular aggregate myopathy Paramyotonia congenita of Von Eulenburg Myotonic dystrophy Distal myopathy with early respiratory muscle involvement Hereditary myopathy with lactic acidosis due to ISCU deficiency Congenital myopathy with excess of thin filaments Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Alpha-crystallinopathy Non-dystrophic myopathy Acquired motor neuron disease Cap myopathy Presynaptic congenital myasthenic syndromes Congenital myopathy with cores Acetazolamide-responsive myotonia Neurogenic scapuloperoneal syndrome, Kaeser type Hereditary inclusion body myopathy type 4 Genetic periodic paralysis X-linked myopathy with postural muscle atrophy Distal hereditary motor neuropathy type 7 Neuromuscular disease Schwartz-Jampel syndrome Genetic skeletal muscle disease Juvenile primary lateral sclerosis Progressive muscular dystrophy Autosomal dominant distal myopathy Inclusion myopathy Autosomal recessive myogenic arthrogryposis multiplex congenita Congenital myotonia Arthrogryposis due to muscular dystrophy Bacterial myositis Juvenile idiopathic inflammatory myopathy Idiopathic inflammatory myopathy Neuromuscular junction disease Motor neuron disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Laminin subunit alpha 2-related congenital muscular dystrophy Duchenne and Becker muscular dystrophy Oculopharyngeal muscular dystrophy Intellectual disability-developmental delay-contractures syndrome Juvenile polymyositis Embryonal rhabdomyosarcoma Muscle filaminopathy Proximal spinal muscular atrophy type 2 Kennedy disease Postsynaptic congenital myasthenic syndromes Andersen-Tawil syndrome Amyotrophic lateral sclerosis type 4 Alpha-B crystallin-related late-onset myopathy Overlap myositis KLHL9-related early-onset distal myopathy Autosomal recessive lower motor neuron disease with childhood onset Laing early-onset distal myopathy Inflammatory myopathy with abundant macrophages Lower motor neuron syndrome with late-adult onset Congenital myopathy Lambert-Eaton myasthenic syndrome Proximal spinal muscular atrophy type 1 Myotonia permanens Autosomal dominant adult-onset proximal spinal muscular atrophy Myosin storage myopathy Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Myasthenia gravis Macrophagic myofasciitis Myofibrillar myopathy Nemaline myopathy Inclusion body myositis Thomsen and Becker disease Cyprus facial-neuromusculoskeletal syndrome Madras motor neuron disease Metabolic myopathy due to lactate transporter defect Hyperkalemic periodic paralysis Congenital muscular dystrophy with integrin alpha-7 deficiency Immune-mediated necrotizing myopathy Distal nebulin myopathy Rhabdomyosarcoma Distal myopathy with posterior leg and anterior hand involvement Acquired skeletal muscle disease Autosomal recessive distal myopathy Trichinellosis Primary lateral sclerosis Congenital myasthenic syndromes with glycosylation defect Ullrich congenital muscular dystrophy Proximal spinal muscular atrophy Eosinophilic fasciitis Autosomal dominant proximal spinal muscular atrophy Brody myopathy Muscular lipidosis Young adult-onset distal hereditary motor neuropathy Periodic paralysis Muscular tumor Viral myositis Infectious, fungal or parasitic myopathy Monomelic amyotrophy Desmin-related myopathy with Mallory body-like inclusions Spinal muscular atrophy associated with central nervous system anomaly Muscular dystrophy Skeletal muscle disease Isaacs syndrome Autosomal recessive distal hereditary motor neuropathy Metabolic myopathy Muscular channelopathy Genetic neuromuscular junction disease Acquired neuromuscular junction disease Spinal atrophy-ophthalmoplegia-pyramidal syndrome Genetic motor neuron disease Tel Hashomer camptodactyly syndrome Congenital lethal myopathy, Compton-North type Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Thyrotoxic periodic paralysis Emery-Dreifuss muscular dystrophy Limb-girdle muscular dystrophy Distal hereditary motor neuropathy type 2 Congenital muscular dystrophy due to dystroglycanopathy Distal hereditary motor neuropathy type 5 Congenital muscular dystrophy due to LMNA mutation Distal spinal muscular atrophy type 3 Distal hereditary motor neuropathy, Jerash type X-linked distal spinal muscular atrophy type 3 Idiopathic camptocormia Congenital fibrosis of extraocular muscles Infantile-onset ascending hereditary spastic paralysis Congenital muscular dystrophy with hyperlaxity Miyoshi myopathy Myotonia fluctuans King-Denborough syndrome DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Juvenile dermatomyositis Morvan syndrome Congenital muscular dystrophy type 1B Congenital myasthenic syndrome Oculopharyngodistal myopathy Desminopathy Distal myotilinopathy Late-onset distal myopathy, Markesbery-Griggs type Synaptic congenital myasthenic syndromes Early-onset myopathy with fatal cardiomyopathy Spinal muscular atrophy with respiratory distress type 1 Finnish upper limb-onset distal myopathy Rippling muscle disease with myasthenia gravis Distal anoctaminopathy Focal myositis Amyotrophic lateral sclerosis Non-dystrophic myopathy with collagen 6 anomaly Muscular dystrophy-white matter spongiosis syndrome Poliomyelitis Bulbospinal muscular atrophy Riboflavin transporter deficiency Hereditary continuous muscle fiber activity Reducing body myopathy Zebra body myopathy Congenital muscular dystrophy Benign Samaritan congenital myopathy Congenital fiber-type disproportion myopathy Cylindrical spirals myopathy Myopathy with hexagonally cross-linked tubular arrays Postpoliomyelitis syndrome Fetal akinesia-cerebral and retinal hemorrhage syndrome Idiopathic eosinophilic myositis Intellectual disability-myopathy-short stature-endocrine defect syndrome