Cytoscape Web
Click node...


2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Idiopathic ventricular fibrillation, not Brugada type
Familial sick sinus syndrome

DPP6 HCN4
SCN5A MYH6
SCN5A


COMMON
GENES
SCN5A



Citations in the biomedical literature:


Idiopathic ventricular fibrillation, not Brugada type
DPP6 SCN5A
Familial sick sinus syndrome
HCN4 MYH6



Idiopathic ventricular fibrillation, not Brugada type
Familial sick sinus syndrome

Synonym(s):
- Familial paroxysmal ventricular fibrillation, not Brugada type

Synonym(s):
- Familial sinus node dysfunction

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D012804

No signs/symptoms info available.