Disease #00025 (FTDALS (dementia, frontotemporal, and/or amyotrophic lateral sclerosis (FTDALS)), OMIM:105550)
| Official abbreviation |
FTDALS |
| Name |
dementia, frontotemporal, and/or amyotrophic lateral sclerosis (FTDALS) |
| OMIM ID |
105550 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
277 |
| Phenotype entries for this disease |
11 |
| Associated with 1 gene |
C9orf72 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-08-03 15:09:30 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|