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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
3 OMIM references -
1 associated gene
No signs/symptoms info
Progressive supranuclear palsy - parkinsonism
Classical progressive supranuclear palsy

MAPT MAPT


COMMON
GENES
MAPT



Citations in the biomedical literature:


Progressive supranuclear palsy - parkinsonism
MAPT
Classical progressive supranuclear palsy



Progressive supranuclear palsy - parkinsonism
Classical progressive supranuclear palsy

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

Synonym(s):
- Classical PSP
- Richardson syndrome
- Steele-Richardson-Olszewski disease

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- 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: elderly
Type of inheritance: sporadic

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

No signs/symptoms info available.