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8 OMIM references -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
3 associated genes
2 signs/symptoms
Generalized epilepsy with febrile seizures-plus context
Paroxysmal extreme pain disorder

GABRD SCN10A
GABRG2 SCN11A
SCN1A SCN9A
SCN1B
SCN2A
SCN9A


COMMON
GENES
SCN9A



Citations in the biomedical literature:


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

Paroxysmal extreme pain disorder
SCN10A SCN11A



Generalized epilepsy with febrile seizures-plus context
Paroxysmal extreme pain disorder

Synonym(s):
- GEFS+

Synonym(s):
- Familial rectal pain

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):
(no data available)

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 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

Paroxysmal extreme pain disorder

Very frequent
- Autosomal dominant inheritance

Frequent
- Constipation



Generalized epilepsy with febrile seizures-plus context

(no data available)