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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Dravet syndrome
Benign familial neonatal-infantile seizures

GABRG2 KCNQ2
PCDH19 SCN2A
SCN1A
SCN1B
SCN2A
SCN9A


COMMON
GENES
SCN2A



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Benign familial neonatal-infantile seizures
KCNQ2



Dravet syndrome
Benign familial neonatal-infantile seizures

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

Synonym(s):
- BFNIS
- Benign neonatal-infantile epilepsy

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:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.