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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Inherited Creutzfeldt-Jakob disease
Hereditary North American Indian childhood cirrhosis

PRNP CIRH1A


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Inherited Creutzfeldt-Jakob disease
PRNP
Hereditary North American Indian childhood cirrhosis
CIRH1A



Inherited Creutzfeldt-Jakob disease
Hereditary North American Indian childhood cirrhosis

Synonym(s):
- Inherited CJD

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.