Cytoscape Web
Click node...

Inherited Creutzfeldt-Jakob disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
X-linked complicated spastic paraplegia type 1
1 associated gene
No signs/symptoms info
Inherited Creutzfeldt-Jakob disease
X-linked complicated spastic paraplegia type 1

PRNP
(UniProt - OMIM)
 L1CAM
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PRNP
(0.59)
L1CAM


Citations in the biomedical literature:


Inherited Creutzfeldt-Jakob disease
PRNP
X-linked complicated spastic paraplegia type 1
L1CAM



Inherited Creutzfeldt-Jakob disease
X-linked complicated spastic paraplegia type 1

Synonym(s):
- Inherited CJD
Synonym(s):
- SPG1
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Certain infectious and parasitic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.