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8 OMIM references -
11 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
6 associated genes
No signs/symptoms info
Brugada syndrome
Dravet syndrome

CACNA1C GABRG2
CACNB2 PCDH19
GPD1L SCN1A
HCN4 SCN1B
KCND3 SCN2A
KCNE3 SCN9A
KCNJ8
SCN1B
SCN3B
SCN5A
TRPM4


COMMON
GENES
SCN1B



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Dravet syndrome
GABRG2 PCDH19 SCN1A SCN2A SCN9A



Brugada syndrome
Dravet syndrome

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

Synonym(s):
- SMEI
- Severe myoclonic epilepsy of infancy

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

Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
- Diseases of the nervous 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: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.