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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 5
8 OMIM references -
6 associated genes
No signs/symptoms info
Dravet syndrome
Generalized epilepsy with febrile seizures-plus context

GABRG2 GABRD
PCDH19 GABRG2
SCN1A SCN1A
SCN1B SCN1B
SCN2A SCN2A
SCN9A SCN9A


COMMON
GENES
GABRG2
SCN1A
SCN1B
SCN2A
SCN9A



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Generalized epilepsy with febrile seizures-plus context
GABRD



Dravet syndrome
Generalized epilepsy with febrile seizures-plus context

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

Synonym(s):
- GEFS+

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: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.