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8 OMIM references -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Brugada syndrome
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

CACNA1C CTNNA3
CACNB2 DSC2
GPD1L DSG2
HCN4 DSP
KCND3 JUP
KCNE3 LMNA
KCNJ8 PKP2
SCN1B RYR2
SCN3B TGFB3
SCN5A TMEM43
TRPM4 TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CACNA1C
(0.75)
RYR2



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Brugada syndrome
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

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

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, classic form
- Familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form
- Familial isolated arrhythmogenic ventricular dysplasia, classic form

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:
(no data available)

External references:
8 OMIM references -
1 MeSH reference: D053840
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.