Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurodegenerative disease
rare disease |
| gptkbp:affects |
central nervous system
|
| gptkbp:affiliatedWith |
prion diseases
|
| gptkbp:alsoKnownAs |
Fatal Familial Insomnia
|
| gptkbp:cause |
death
|
| gptkbp:causedBy |
mutation in PRNP gene
|
| gptkbp:characterizedBy |
cognitive decline
autonomic dysfunction motor disturbances progressive insomnia |
| gptkbp:firstDescribed |
1986
Elio Lugaresi |
| gptkbp:hasNoCure |
true
|
| https://www.w3.org/2000/01/rdf-schema#label |
Lugaresi disease
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:bfsParent |
gptkb:fatal_familial_insomnia
|
| gptkbp:bfsLayer |
7
|