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
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