SE-ATLAS

Immune-mediated necrotizing myopathy Mitochondrial myopathy Thomsen and Becker disease Primary lateral sclerosis Chronic inflammatory demyelinating polyneuropathy Hereditary ATTR amyloidosis Variant of Guillain-Barré syndrome Facioscapulohumeral dystrophy Amyotrophic lateral sclerosis Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Guillain-Barré syndrome Proximal spinal muscular atrophy Myasthenia gravis Congenital myasthenic syndrome Duchenne muscular dystrophy Polymyositis Dermatomyositis Inclusion body myositis Lambert-Eaton myasthenic syndrome Limb-girdle muscular dystrophy Hereditary spastic paraplegia Autosomal dominant cerebellar ataxia type I Autosomal dominant cerebellar ataxia type IV Autosomal dominant cerebellar ataxia type III Becker muscular dystrophy Autosomal dominant cerebellar ataxia Autosomal dominant cerebellar ataxia type II Spinocerebellar ataxia type 29 Autosomal dominant intermediate Charcot-Marie-Tooth disease Duchenne and Becker muscular dystrophy Spinocerebellar ataxia type 38 Autosomal recessive axonal hereditary motor and sensory neuropathy Spastic paraplegia-optic atrophy-neuropathy syndrome Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Non-progressive cerebellar ataxia with intellectual disability Acetazolamide-responsive myotonia Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Spinocerebellar ataxia type 34 X-linked Charcot-Marie-Tooth disease type 6 Autosomal dominant hereditary demyelinating motor and sensory neuropathy Autosomal recessive hereditary demyelinating motor and sensory neuropathy Spinocerebellar ataxia type 41 Autosomal dominant hereditary axonal motor and sensory neuropathy Paramyotonia congenita of Von Eulenburg Autosomal recessive spastic paraplegia type 74 Spinocerebellar ataxia type 42 Autosomal recessive intermediate Charcot-Marie-Tooth disease Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 37 Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 7 PUM1-associated developmental disability-ataxia-seizure syndrome Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 17 X-linked Charcot-Marie-Tooth disease type 5 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 10 Spinocerebellar ataxia type 8 Axonal hereditary motor and sensory neuropathy Spinocerebellar ataxia type 14 Spinocerebellar ataxia type 30 Spinocerebellar ataxia type 12 Spinocerebellar ataxia type 4 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 5 Spinocerebellar ataxia type 15/16 Spinocerebellar ataxia type 13 Spinocerebellar ataxia type 18 Spinocerebellar ataxia type 32 X-linked Charcot-Marie-Tooth disease type 3 X-linked Charcot-Marie-Tooth disease type 2 X-linked Charcot-Marie-Tooth disease type 4 Spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 35 Autosomal recessive spastic paraplegia type 57 Spinocerebellar ataxia type 40 X-linked Charcot-Marie-Tooth disease type 1 Demyelinating hereditary motor and sensory neuropathy Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 19/22 Spinocerebellar ataxia type 46 Intermediate Charcot-Marie-Tooth disease Proximal myotonic myopathy Spinocerebellar ataxia type 45 Spinocerebellar ataxia type 43 X-linked Charcot-Marie-Tooth disease Digital extensor muscle aplasia-polyneuropathy Autosomal recessive spastic paraplegia type 55 Spinocerebellar ataxia type 28 Spinocerebellar ataxia type 23 Spinocerebellar ataxia type 25 Spinocerebellar ataxia type 26 Spinocerebellar ataxia type 20 Subacute inflammatory demyelinating polyneuropathy Refsum disease Emery-Dreifuss muscular dystrophy Lewis-Sumner syndrome Progressive muscular dystrophy Juvenile myasthenia gravis Polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies Bethlem muscular dystrophy CANOMAD syndrome Myotonic syndrome Hereditary motor and sensory neuropathy Muscular dystrophy Cerebellar ataxia with peripheral neuropathy Neuromuscular junction disease Congenital muscular dystrophy