Cytoscape Web
Click node...

Dravet syndrome
1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
Female restricted epilepsy with intellectual deficit
1 OMIM reference -
1 associated gene
No signs/symptoms info
Dravet syndrome
Female restricted epilepsy with intellectual deficit

GABRG2
(UniProt - OMIM)
 PCDH19
(UniProt - OMIM)
PCDH19
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)
SCN1B
(UniProt - OMIM)
SCN2A
(UniProt - OMIM)
SCN9A
(UniProt - OMIM)

COMMON
GENES 		PCDH19


Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Female restricted epilepsy with intellectual deficit



Dravet syndrome
Female restricted epilepsy with intellectual deficit

Synonym(s):
- SMEI
- Severe myoclonic epilepsy of infancy
Synonym(s):
- EFMR
- Familial epilepsy and mental retardation limited to females
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):
(no data available)
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: unknown
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.