SE-ATLAS

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