Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:neurodegenerative_disease
gptkb:prion_disease |
| gptkbp:alternativeName |
gptkb:fCJD
|
| gptkbp:causedBy |
mutation in PRNP gene
|
| gptkbp:diagnosedBy |
gptkb:EEG
MRI genetic testing CSF analysis |
| gptkbp:duration |
months to a few years
|
| gptkbp:frequency |
rare
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:onset |
middle age
|
| gptkbp:prognosis |
fatal
|
| gptkbp:riskFactor |
family history of CJD
|
| gptkbp:subspecies |
gptkb:Creutzfeldt-Jakob_disease
|
| gptkbp:symptom |
gptkb:dementia
behavioral changes ataxia myoclonus |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:Creutzfeldt–Jakob_disease
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
familial CJD
|