Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurodegenerative disease
|
| gptkbp:abbreviation |
gptkb:FTDP-17
|
| gptkbp:associatedWith |
MAPT gene mutation
|
| gptkbp:category |
gptkb:tauopathy
|
| gptkbp:causedBy |
tau protein dysfunction
|
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:firstDescribed |
1996
|
| gptkbp:fullName |
Frontotemporal dementia and parkinsonism linked to chromosome 17
|
| https://www.w3.org/2000/01/rdf-schema#label |
FTDP-17
|
| gptkbp:ICD-10_code |
G31.0
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_17
|
| gptkbp:OMIM |
600274
|
| gptkbp:onset |
adult
|
| gptkbp:riskFactor |
family history
|
| gptkbp:symptom |
behavioral changes
cognitive decline movement disorders frontotemporal dementia parkinsonism |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:MAPT
gptkb:HGNC:7611 |
| gptkbp:bfsLayer |
7
|