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8 OMIM references -
11 associated genes
No signs/symptoms info
COMMON GENES: 3
5 OMIM references -
4 associated genes
1 sign/symptom
Brugada syndrome
Familial progressive cardiac conduction defect

CACNA1C NKX2-5
CACNB2 SCN1B
GPD1L SCN5A
HCN4 TRPM4
KCND3
KCNE3
KCNJ8
SCN1B
SCN3B
SCN5A
TRPM4


COMMON
GENES
SCN1B
SCN5A
TRPM4



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Familial progressive cardiac conduction defect
NKX2-5



Brugada syndrome
Familial progressive cardiac conduction defect

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

Synonym(s):
- Familial Lenègre disease
- Familial Lev disease
- Familial Lev-Lenègre disease
- Familial PCCD
- Familial progressive heart block
- Hereditary bundle branch defect

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: <1 / 1 000 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant

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

Familial progressive cardiac conduction defect

Frequent
- Cardiac rhythm disorder / arrhythmia



Brugada syndrome

(no data available)