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8 OMIM references -
11 associated genes
No signs/symptoms info
COMMON GENES: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Brugada syndrome
Idiopathic ventricular fibrillation, not Brugada type

CACNA1C DPP6
CACNB2 SCN5A
GPD1L
HCN4
KCND3
KCNE3
KCNJ8
SCN1B
SCN3B
SCN5A
TRPM4


COMMON
GENES
SCN5A



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Idiopathic ventricular fibrillation, not Brugada type
DPP6



Brugada syndrome
Idiopathic ventricular fibrillation, not Brugada type

Synonym(s):
- Bangungut
- Dream disease
- Idiopathic ventricular fibrillation, Brugada type
- Pokkuri death syndrome
- SUNDS
- Sudden unexplained nocturnal death syndrome

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):
- Diseases of the circulatory system -
Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
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:
8 OMIM references -
1 MeSH reference: D053840
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.