Disease #00010 (FTLD (Frontotemporal Lobar Degeneration), OMIM:607485)
| Official abbreviation |
FTLD |
| Name |
Frontotemporal Lobar Degeneration |
| OMIM ID |
607485 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
355 |
| Phenotype entries for this disease |
3 |
| Associated with 22 genes |
CCNF, CHCHD10, CHMP2B, CYLD, FUS, GFAP, GRN, GSK3B, LRRK2, MAPT, NEK1, NOTCH3, OPTN, PRNP, PSEN1, SOD1, SQSTM1, TARDBP, TBK1, TREM2, UBQLN2, VCP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|