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Creutzfeldt Jacob disease

Disease Summary
Associated Targets (36)
Tbio

23

Tdark

6

Tchem

5

Tclin

2


Explore Associated Targets
Mondo Description A rare transmittable degenerative disorder of the brain caused by prions. Morphologically it is characterized by spongiform degeneration of the cerebral and cerebellar cortex. Signs and symptoms include sleep disturbances, personality changes, aphasia, ataxia, muscle atrophy and weakness, visual loss, and myoclonus. It usually leads to death within a year from the onset of the disease.
Mondo Term and Equivalent IDs
MONDO:0005357:  Creutzfeldt Jacob disease
COHD:372241: 
EFO:0004226: 
GARD:0006956: 
ICD9:046.1: 
MESH:D007562: 
NCIT:C26802: 
SCTID:792004: 
GWAS Targets (3)
Target
TDL
Study Count
SNP Count
Beta Count
Odds Ratio
Evidence (Mean Rank Score)
Provenance
Tbio
1
1
0
3.3
21.5
Tbio
1
1
0
3.3
21.5
Tbio
1
1
0
3
0.4
Target
TDL
Beta Count
Odds Ratio
Evidence (Mean Rank Score)
Provenance
Tbio
0
3.3
21.5
Tbio
0
3.3
21.5
Tbio
0
3
0.4
Target Novelty (Tin-x)