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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fatal familial insomnia
Gerstmann-Straussler-Scheinker syndrome

PRNP PRNP


COMMON
GENES
PRNP



Citations in the biomedical literature:


Fatal familial insomnia
PRNP
Gerstmann-Straussler-Scheinker syndrome



Fatal familial insomnia
Gerstmann-Straussler-Scheinker syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Subacute spongiform encephalopathy, Gerstmann-Straussler type

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

Classification (ICD10):
- Certain infectious and parasitic diseases -
Classification (ICD10):
- Certain infectious and parasitic diseases -

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: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D034062
External references:
1 OMIM reference -
1 MeSH reference: D016098

No signs/symptoms info available.