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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
6 associated genes
No signs/symptoms info
Semantic dementia
Dravet syndrome

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


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Dravet syndrome
GABRG2 PCDH19 SCN1A SCN1B SCN2A SCN9A



Semantic dementia
Dravet syndrome

Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA

Synonym(s):
- SMEI
- Severe myoclonic epilepsy 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):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.