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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
9 OMIM references -
10 associated genes
No signs/symptoms info
Dravet syndrome
Early infantile epileptic encephalopathy

GABRG2 ARX
PCDH19 CACNA2D2
SCN1A GNAO1
SCN1B KCNQ2
SCN2A PLCB1
SCN9A SCN2A
SCN8A
SLC25A22
SPTAN1
STXBP1


COMMON
GENES
SCN2A



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Early infantile epileptic encephalopathy
ARX CACNA2D2 GNAO1 KCNQ2 PLCB1
SCN8A SLC25A22 SPTAN1 STXBP1



Dravet syndrome
Early infantile epileptic encephalopathy

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

Synonym(s):
- EIEE
- Early infantile epileptic encephalopathy with suppression-bursts
- Ohtahara syndrome

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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.