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
|
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