Disease #00096 (FTD (dementia, frontotemporal (FTD)), OMIM:600274)
| Official abbreviation |
FTD |
| Name |
dementia, frontotemporal (FTD) |
| OMIM ID |
600274 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
429 |
| Phenotype entries for this disease |
61 |
| Associated with 2 genes |
MAPT, PSEN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-12-10 14:01:50 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|