List of diseases covered by
Amyotrophic Lateral Sclerosis NGS panel
| Gene | Condition |
| ALS2 | Amyotrophic lateral sclerosis 2, juvenile; Primary lateral sclerosis, juvenile; Spastic paralysis, infantile onset ascending |
| ANG | Amyotrophic lateral sclerosis 9 |
| CHCHD10 | Frontotemporal dementia and/or amyotrophic lateral sclerosis 2; Myopathy, isolated mitochondrial, autosomal dominant; Spinal muscular atrophy, Jokela type |
| CHMP2B | Amyotrophic lateral sclerosis 17; Dementia, familial, nonspecific |
| ERBB4 | Amyotrophic lateral sclerosis 19 |
| FIG4 | Amyotrophic lateral sclerosis 11; Charcot-Marie-Tooth disease, type 4J; Yunis-Varon syndrome |
| FUS | Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia; Essential tremor, hereditary, 4 |
| MATR3 | Amyotrophic lateral sclerosis 21 |
| OPTN | Amyotrophic lateral sclerosis 12 |
| PFN1 | Amyotrophic lateral sclerosis 18 |
| SETX | Amyotrophic lateral sclerosis 4, juvenile; Spinocerebellar ataxia, autosomal recessive 1 |
| SIGMAR1 | Amyotrophic lateral sclerosis 16, juvenile; Spinal muscular atrophy, distal, autosomal recessive, 2 |
| SOD1 | Amyotrophic lateral sclerosis 1 |
| SPART | Troyer syndrome |
| SPG11 | Amyotrophic lateral sclerosis 5, juvenile; Charcot-Marie-Tooth disease, axonal, type 2X; Spastic paraplegia 11, autosomal recessive |
| SQSTM1 | Frontotemporal dementia and/or amyotrophic lateral sclerosis 3; Myopathy, distal, with rimmed vacuoles; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset; Paget disease of bone 3 |
| TARDBP | Amyotrophic lateral sclerosis 10, with or without FTD; Frontotemporal lobar degeneration, TARDBP-related |
| TBK1 | Frontotemporal dementia and/or amyotrophic lateral sclerosis 4; |
| TUBA4A | Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia |
| UBQLN2 | Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia |
| VAPB | Amyotrophic lateral sclerosis 8; Spinal muscular atrophy, late-onset, Finkel type |
| VCP | Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia; Charcot-Marie-Tooth disease, type 2Y; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1 |

