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8 OMIM references -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
9 OMIM references -
10 associated genes
No signs/symptoms info
Generalized epilepsy with febrile seizures-plus context
Early infantile epileptic encephalopathy

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


COMMON
GENES
SCN2A



Citations in the biomedical literature:


Generalized epilepsy with febrile seizures-plus context
GABRD GABRG2 SCN1A SCN1B SCN2A SCN9A

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



Generalized epilepsy with febrile seizures-plus context
Early infantile epileptic encephalopathy

Synonym(s):
- GEFS+

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: childhood
Average age of death: normal
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:
8 OMIM references -
No MeSH references
External references:
9 OMIM references -
No MeSH references

No signs/symptoms info available.