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Hereditary North American Indian childhood cirrhosis
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial Alzheimer-like prion disease
1 associated gene
No signs/symptoms info
Hereditary North American Indian childhood cirrhosis
Familial Alzheimer-like prion disease

CIRH1A
(UniProt - OMIM)
 PRNP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CIRH1A
(0.68)
PRNP


Citations in the biomedical literature:


Hereditary North American Indian childhood cirrhosis
CIRH1A
Familial Alzheimer-like prion disease
PRNP



Hereditary North American Indian childhood cirrhosis
Familial Alzheimer-like prion disease

Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Certain infectious and parasitic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.