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

HCN4 DPP6
MYH6 SCN5A
SCN5A


COMMON
GENES
SCN5A



Citations in the biomedical literature:


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



Familial sick sinus syndrome
Idiopathic ventricular fibrillation, not Brugada type

Synonym(s):
- Familial sinus node dysfunction

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

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

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

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

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

No signs/symptoms info available.