Cytoscape Web
Click node...


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
Huntington disease-like 1

PRNP PRNP


COMMON
GENES
PRNP



Citations in the biomedical literature:


Fatal familial insomnia
PRNP
Huntington disease-like 1



Fatal familial insomnia
Huntington disease-like 1

Synonym(s):
(no synonyms)

Synonym(s):
- Early onset prion disease with prominent psychiatric features
- HDL1

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):
(no data available)

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: -
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 -
No MeSH references

No signs/symptoms info available.