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8 OMIM references -
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
16 OMIM references -
4 associated genes
No signs/symptoms info
Generalized epilepsy with febrile seizures-plus context
Early-onset autosomal dominant Alzheimer disease

GABRD APP
GABRG2 PSEN1
SCN1A PSEN2
SCN1B SORL1
SCN2A
SCN9A


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Generalized epilepsy with febrile seizures-plus context
GABRD GABRG2 SCN1A SCN1B SCN2A SCN9A

Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Generalized epilepsy with febrile seizures-plus context
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- GEFS+

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

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: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
8 OMIM references -
No MeSH references
External references:
16 OMIM references -
No MeSH references

No signs/symptoms info available.