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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Fatal familial insomnia
Progressive supranuclear palsy - corticobasal syndrome

PRNP MAPT


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Fatal familial insomnia
PRNP
Progressive supranuclear palsy - corticobasal syndrome
MAPT



Fatal familial insomnia
Progressive supranuclear palsy - corticobasal syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- PSP-CBS
- PSP-corticobasal syndrome

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

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

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

External references:
1 OMIM reference -
1 MeSH reference: D034062
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.