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FG syndrome type 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary chronic pancreatitis
1 OMIM reference -
5 associated genes
No signs/symptoms info
FG syndrome type 1
Hereditary chronic pancreatitis

MED12
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
CTRC
(UniProt - OMIM)
PRSS1
(UniProt - OMIM)
PRSS2
(UniProt - OMIM)
SPINK1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MED12
(0.63)
CFTR


Citations in the biomedical literature:


FG syndrome type 1
MED12
Hereditary chronic pancreatitis
CFTR CTRC PRSS1 PRSS2 SPINK1



FG syndrome type 1
Hereditary chronic pancreatitis

Synonym(s):
- Opitz-Kaveggia syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
(no data available)
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.