Disease #02665 (FTLDTDP;PPA (degeneration, frontotemporal lobar, with TDP43 inclusions (FTLD-TDP, aphasia, primary progressive (PPA))), OMIM:607485)
| Official abbreviation |
FTLDTDP;PPA |
| Name |
degeneration, frontotemporal lobar, with TDP43 inclusions (FTLD-TDP, aphasia, primary progressive (PPA)) |
| OMIM ID |
607485 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GRN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|