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1 OMIM reference -
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
6 associated genes
No signs/symptoms info
Dravet syndrome
Behavioral variant of frontotemporal dementia

GABRG2 C9ORF72
PCDH19 CHMP2B
SCN1A GRN
SCN1B MAPT
SCN2A PSEN1
SCN9A VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SCN1A
(0.63)
PSEN1



Citations in the biomedical literature:


Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A

Behavioral variant of frontotemporal dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Dravet syndrome
Behavioral variant of frontotemporal dementia

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

Synonym(s):
- bv-FTD

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: unknown
Average age onset: adulthood
Average age of death: elderly
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.