- CODEDESCRIPTIONNUMBER OF GENES
-
7-1
Amyotrophic lateral sclerosis25
-
7-2
Ataxia351
-
7-3
Autism spectrum disorders101
-
7-4
Comprehensive panel muscular dystrophy & congenital myopathy129
-
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