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

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


COMMON
GENES
SCN1B



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN3B SCN5A TRPM4



Dravet syndrome
Brugada syndrome

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

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

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.