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Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
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
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Hereditary chronic pancreatitis

LMNA
(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)
LMNA
(0.63)
CFTR


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Hereditary chronic pancreatitis
CFTR CTRC PRSS1 PRSS2 SPINK1



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Hereditary chronic pancreatitis

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic 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: unknown
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.