Cytoscape Web
Click node...


1 OMIM reference -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
4 OMIM references -
4 associated genes
9 signs/symptoms
Dravet syndrome
Familial or sporadic hemiplegic migraine

GABRG2 ATP1A2
PCDH19 CACNA1A
SCN1A PRRT2
SCN1B SCN1A
SCN2A
SCN9A


COMMON
GENES
SCN1A



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Familial or sporadic hemiplegic migraine
ATP1A2 CACNA1A PRRT2



Dravet syndrome
Familial or sporadic hemiplegic migraine

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: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references

Familial or sporadic hemiplegic migraine

Very frequent
- Autosomal dominant inheritance
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Movement disorder

Frequent
- Ataxia / incoordination / trouble of the equilibrium
- Nystagmus

Occasional
- EEG anomalies
- Retinitis pigmentosa / retinal pigmentary changes
- Sensorineural deafness / hearing loss
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia


Dravet syndrome

(no data available)