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8 OMIM references -
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
2 associated genes
No signs/symptoms info
Generalized epilepsy with febrile seizures-plus context
Autosomal dominant cervical dystonia

GABRD ANO3
GABRG2 DRD5
SCN1A
SCN1B
SCN2A
SCN9A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GABRG2
(0.79)
DRD5



Citations in the biomedical literature:


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

Autosomal dominant cervical dystonia
ANO3 DRD5



Generalized epilepsy with febrile seizures-plus context
Autosomal dominant cervical dystonia

Synonym(s):
- GEFS+

Synonym(s):
- Autosomal dominant spasmodic torticollis

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: normal
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.