Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Progressive supranuclear palsy - parkinsonism
Familial Alzheimer-like prion disease

MAPT PRNP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPT
(0.49)
PRNP



Citations in the biomedical literature:


Progressive supranuclear palsy - parkinsonism
MAPT
Familial Alzheimer-like prion disease
PRNP



Progressive supranuclear palsy - parkinsonism
Familial Alzheimer-like prion disease

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

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Certain infectious and parasitic diseases -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.