SE-ATLAS

Allan-Herndon-Dudley syndrome Alpers-Huttenlocher syndrome Amyotrophic lateral sclerosis Andersen-Tawil syndrome Autosomal dominant spastic paraplegia type 10 Autosomal dominant spastic paraplegia type 12 Autosomal dominant spastic paraplegia type 13 Autosomal dominant spastic paraplegia type 19 Autosomal dominant spastic paraplegia type 3 Autosomal dominant spastic paraplegia type 31 Autosomal dominant spastic paraplegia type 37 Autosomal dominant spastic paraplegia type 4 Autosomal dominant spastic paraplegia type 41 Autosomal dominant spastic paraplegia type 42 Autosomal dominant spastic paraplegia type 6 Autosomal dominant spastic paraplegia type 8 Autosomal recessive spastic paraplegia type 11 Autosomal recessive spastic paraplegia type 14 Autosomal recessive spastic paraplegia type 15 Autosomal recessive spastic paraplegia type 20 Autosomal recessive spastic paraplegia type 21 Autosomal recessive spastic paraplegia type 23 Autosomal recessive spastic paraplegia type 24 Autosomal recessive spastic paraplegia type 25 Autosomal recessive spastic paraplegia type 26 Autosomal recessive spastic paraplegia type 27 Autosomal recessive spastic paraplegia type 28 Autosomal recessive spastic paraplegia type 32 Autosomal recessive spastic paraplegia type 35 Autosomal recessive spastic paraplegia type 39 Autosomal recessive spastic paraplegia type 43 Autosomal recessive spastic paraplegia type 44 Autosomal recessive spastic paraplegia type 45 Autosomal recessive spastic paraplegia type 46 Autosomal recessive spastic paraplegia type 48 Autosomal recessive spastic paraplegia type 53 Autosomal recessive spastic paraplegia type 54 Autosomal recessive spastic paraplegia type 55 Autosomal recessive spastic paraplegia type 56 Autosomal recessive spastic paraplegia type 5A Autosomal spastic paraplegia type 18 Autosomal spastic paraplegia type 30 Becker muscular dystrophy Complex regional pain syndrome type 1 Complex regional pain syndrome type 2 Duchenne and Becker muscular dystrophy Duchenne muscular dystrophy Genetic periodic paralysis Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Hereditary spastic paraplegia Hyperkalemic periodic paralysis Hypokalemic periodic paralysis MASA syndrome MT-ATP6-related mitochondrial spastic paraplegia Macrocephaly-spastic paraplegia-dysmorphism syndrome Menkes disease Mutilating hereditary sensory neuropathy with spastic paraplegia Postpoliomyelitis syndrome Pure or complex X-linked spastic paraplegia Pure or complex autosomal dominant spastic paraplegia Pure or complex autosomal recessive spastic paraplegia Severe intellectual disability and progressive spastic paraplegia Spastic paraplegia type 2 Spastic paraplegia type 7 Spastic paraplegia-glaucoma-intellectual disability syndrome Spastic paraplegia-optic atrophy-neuropathy syndrome Thalidomide embryopathy X-linked pure spastic paraplegia X-linked spastic paraplegia type 16 X-linked spastic paraplegia type 34