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

GABRD CHD2
GABRG2 MAPK10
SCN1A SCN1A
SCN1B
SCN2A
SCN9A


COMMON
GENES
SCN1A



Citations in the biomedical literature:


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

Lennox-Gastaut syndrome
CHD2 MAPK10



Generalized epilepsy with febrile seizures-plus context
Lennox-Gastaut syndrome

Synonym(s):
- GEFS+

Synonym(s):
(no synonyms)

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: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
8 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: C535500

No signs/symptoms info available.