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1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
3 OMIM references -
5 associated genes
No signs/symptoms info
Dravet syndrome
Malignant migrating partial seizures of infancy

GABRG2 KCNT1
PCDH19 PLCB1
SCN1A SCN1A
SCN1B SLC25A22
SCN2A TBC1D24
SCN9A


COMMON
GENES
SCN1A



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Malignant migrating partial seizures of infancy
KCNT1 PLCB1 SLC25A22 TBC1D24



Dravet syndrome
Malignant migrating partial seizures of infancy

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

Synonym(s):
- MMPEI
- MMPSI
- MPEI
- MPSI
- Malignant migrating partial epilepsy of infancy
- Migrating partial epilepsy of infancy
- Migrating partial seizures of infancy

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):
(no data available)

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: 1-9 / 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:
3 OMIM references -
No MeSH references

No signs/symptoms info available.