Cytoscape Web
Click node...

Idiopathic ventricular fibrillation, not Brugada type
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Rippling muscle disease
2 OMIM references -
1 associated gene
No signs/symptoms info
Idiopathic ventricular fibrillation, not Brugada type
Rippling muscle disease

DPP6
(UniProt - OMIM)
 CAV3
(UniProt - OMIM)
SCN5A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SCN5A
(0.63)
CAV3


Citations in the biomedical literature:


Idiopathic ventricular fibrillation, not Brugada type
DPP6 SCN5A
Rippling muscle disease
CAV3



Idiopathic ventricular fibrillation, not Brugada type
Rippling muscle disease

Synonym(s):
- Familial paroxysmal ventricular fibrillation, not Brugada type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C535685
No signs/symptoms info available.