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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Inherited Creutzfeldt-Jakob disease
Progressive supranuclear palsy - pure akinesia with gait freezing

PRNP MAPT


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Inherited Creutzfeldt-Jakob disease
PRNP
Progressive supranuclear palsy - pure akinesia with gait freezing
MAPT



Inherited Creutzfeldt-Jakob disease
Progressive supranuclear palsy - pure akinesia with gait freezing

Synonym(s):
- Inherited CJD

Synonym(s):
- PSP-PAGF
- PSP-pure akinesia with gait freezing

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:
(no data available)
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:
No OMIM references
No MeSH references

No signs/symptoms info available.