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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
3 associated genes
No signs/symptoms info
Dravet syndrome
Lennox-Gastaut syndrome

GABRG2 CHD2
PCDH19 MAPK10
SCN1A SCN1A
SCN1B
SCN2A
SCN9A


COMMON
GENES
SCN1A



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Lennox-Gastaut syndrome
CHD2 MAPK10



Dravet syndrome
Lennox-Gastaut syndrome

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

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: neonatal/infancy
Average age of death: any age
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:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: C535500

No signs/symptoms info available.