Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Progressive supranuclear palsy - parkinsonism

APP MAPT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.79)
MAPT



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Progressive supranuclear palsy - parkinsonism
MAPT



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Progressive supranuclear palsy - parkinsonism

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- PSP-p
- PSP-parkinsonism

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.