SE-ATLAS

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