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5 OMIM references -
8 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Primary biliary cirrhosis
Hereditary chronic pancreatitis

IL12A CFTR
IL12RB1 CTRC
IRF5 PRSS1
MMEL1 PRSS2
POU2AF1 SPINK1
SPIB
TNFSF15
TNPO3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TNPO3
(0.63)
CFTR



Citations in the biomedical literature:


Primary biliary cirrhosis
IL12A IL12RB1 IRF5 MMEL1 POU2AF1 SPIB
TNFSF15 TNPO3
Hereditary chronic pancreatitis
CFTR CTRC PRSS1 PRSS2 SPINK1



Primary biliary cirrhosis
Hereditary chronic pancreatitis

Synonym(s):
- Hanot syndrome

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare hepatic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Diseases of the digestive system -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.