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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
Idiopathic bronchiectasis
3 OMIM references -
4 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Idiopathic bronchiectasis

LMNA
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
SCNN1A
(UniProt - OMIM)
SCNN1B
(UniProt - OMIM)
SCNN1G
(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
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Idiopathic bronchiectasis

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare respiratory disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the respiratory system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.