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Lennox-Gastaut syndrome
3 associated genes
No signs/symptoms info
COMMON GENES: 2
Epilepsy with myoclonic-astatic seizures
3 associated genes
No signs/symptoms info
Lennox-Gastaut syndrome
Epilepsy with myoclonic-astatic seizures

CHD2
(UniProt - OMIM)
 CHD2
(UniProt - OMIM)
MAPK10
(UniProt - OMIM)
 SCN1A
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)
 SLC2A1
(UniProt - OMIM)

COMMON
GENES 		CHD2
SCN1A


Citations in the biomedical literature:


Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A
Epilepsy with myoclonic-astatic seizures
SLC2A1



Lennox-Gastaut syndrome
Epilepsy with myoclonic-astatic seizures

Synonym(s):
(no synonyms)

Synonym(s):
- Doose syndrome
- EMAS
- Epilepsy with myoclonic-atonic seizures
- MAE
- Myoclonic atonic epilepsy
- Myoclonic-astatic epilepsy in early childhood
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: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: unknown
External references:
No OMIM references
1 MeSH reference: C535500
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.