Cytoscape Web
Click node...

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Extraskeletal Ewing sarcoma
4 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Extraskeletal Ewing sarcoma

LMNA
(UniProt - OMIM)
 ERG
(UniProt - OMIM)
EWSR1
(UniProt - OMIM)
FLI1
(UniProt - OMIM)
SMARCA5
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.49)
SMARCA5


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Extraskeletal Ewing sarcoma
ERG EWSR1 FLI1 SMARCA5



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Extraskeletal Ewing sarcoma

Synonym(s):
(no synonyms)

Synonym(s):
- EOE
- Extraosseous Ewing sarcoma
- Extraosseous Ewing tumor
- Extraskeletal Ewing tumor
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
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:
No OMIM references
No MeSH references
No signs/symptoms info available.