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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
4 OMIM references -
6 associated genes
No signs/symptoms info
Dravet syndrome
Childhood absence epilepsy

GABRG2 CACNA1H
PCDH19 GABRA1
SCN1A GABRB3
SCN1B GABRG2
SCN2A JRK
SCN9A SLC2A1


COMMON
GENES
GABRG2



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Childhood absence epilepsy
CACNA1H GABRA1 GABRB3 JRK SLC2A1



Dravet syndrome
Childhood absence epilepsy

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

Synonym(s):
- Pyknolepsy

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous 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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.