- CODEDESCRIPTIONNUMBER OF GENES
 
- 
									7-1
									Amyotrophic lateral sclerosis25
 - 
									7-2
									Ataxia351
 - 
									7-3
									Autism spectrum disorders101
 - 
									7-4
									Comprehensive panel muscular dystrophy & congenital myopathy128
 - 
									7-6
									Early onset dementia & dementia in older adults34
 - 
									7-7
									Emery-Dreyfuss muscular dystrophy28
 - 
									7-8
									Epilepsy557
 - 
									7-9
									Hereditary neuropathies (includes Charcot-Marie-Tooth)174
 - 
									7-10
									Hereditary spastic paraparesis90
 - 
									7-11
									Infantile nystagmus10
 - 
									7-12
									Leukodystrophy - white matter disease126
 - 
									7-14
									Limb girdle muscular dystrophy64
 - 
									7-15
									Neurofibromatosis30
 - 
									7-16
									Neuromuscular disorders comprehensive panel209
 - 
									7-17
									Parkinson disease40
 - 
									7-18
									Spinal muscular atrophy24
 - 
									2-8
									Tuberous sclerosis2
 - 
									7-20
									X-linked intellectual disability107
 - 
									7-5
									Dystonia, chorea and other hyperkinetic movement disorders197
 - 
									7-13
									Leukodystrophy- White Matter Disease Early Onset1932