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PROTEIN INTERACTIONS: 2
1 OMIM reference -
5 associated genes
No signs/symptoms info
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Hereditary chronic pancreatitis

SERPINA1 CFTR
CTRC
PRSS1
PRSS2
SPINK1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SERPINA1
SERPINA1
(0.52)
(0.52)
PRSS1
PRSS2



Citations in the biomedical literature:


Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
SERPINA1
Hereditary chronic pancreatitis
CFTR CTRC PRSS1 PRSS2 SPINK1



Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Hereditary chronic pancreatitis

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the digestive system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
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:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.