FEBRILE SEIZURES, FAMILIAL, 9

General Information (adopted from Orphanet):

Synonyms, Signs: FEBRILE CONVULSIONS, FAMILIAL, 9
FEB9
Number of Symptoms 6
OrphanetNr:
OMIM Id: 611634
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0010849) EEG with spike-wave complexes (>3.5 Hz) 6 / 7739
2
(HPO:0002373) Febrile seizures 37 / 7739
3
(HPO:0002121) Absence seizures 62 / 7739
4
(OMIM) EEG shows 3-Hz spike-wave discharges 1 / 7739
5
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
6
(OMIM) Childhood absence seizures 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Nabbout et al. (2007) reported a 4-generation French family in which 13 individuals had febrile seizures. Age at onset ranged from 6 months to 3 years, and resolved by age 5 years in all but 1 patient, who ...