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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
16 OMIM references -
4 associated genes
No signs/symptoms info
Progressive supranuclear palsy - parkinsonism
Early-onset autosomal dominant Alzheimer disease

MAPT APP
PSEN1
PSEN2
SORL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPT
MAPT
(0.79)
(0.55)
APP
PSEN1



Citations in the biomedical literature:


Progressive supranuclear palsy - parkinsonism
MAPT
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Progressive supranuclear palsy - parkinsonism
Early-onset autosomal dominant Alzheimer disease

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

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.