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Inherited Creutzfeldt-Jakob disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Inherited Creutzfeldt-Jakob disease
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

PRNP
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PRNP
(0.88)
APP


Citations in the biomedical literature:


Inherited Creutzfeldt-Jakob disease
PRNP
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Inherited Creutzfeldt-Jakob disease
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Inherited CJD
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic 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:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.