| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
R-numbers: R58 Signed-off version 6.6 | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Phenotypes Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, OMIM:300857 |