SE-ATLAS

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