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
|