Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:causedBy |
mutation in PRNP gene
|
| gptkbp:diagnosedBy |
clinical evaluation
genetic testing |
| gptkbp:firstDescribed |
1980s
|
| gptkbp:frequency |
rare
|
| gptkbp:fullName |
familial Creutzfeldt-Jakob disease
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:isA |
gptkb:neurodegenerative_disease
gptkb:prion_disease |
| gptkbp:mortalityRate |
high
|
| gptkbp:onset |
middle age
|
| gptkbp:prognosis |
poor
|
| gptkbp:progression |
gptkb:fire
|
| gptkbp:relatedTo |
gptkb:variant_Creutzfeldt-Jakob_disease
sporadic Creutzfeldt-Jakob disease |
| gptkbp:symptom |
gptkb:dementia
ataxia myoclonus |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:familial_CJD
|
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
fCJD
|