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Generalized epilepsy with febrile seizures-plus context
8 OMIM references -
6 associated genes
35 connected diseases
No signs/symptoms info
Disease Type of connection
Dravet syndrome
1p36 deletion syndrome
Benign familial infantile seizures
Benign familial neonatal-infantile seizures
Brugada syndrome
Channelopathy-associated congenital insensitivity to pain
Childhood absence epilepsy
Early infantile epileptic encephalopathy
Epilepsy with myoclonic-astatic seizures
Erythromelalgia
Familial atrial fibrillation
Familial or sporadic hemiplegic migraine
Familial progressive cardiac conduction defect
Hereditary sensory and autonomic neuropathy type 2
Juvenile myoclonic epilepsy
Lennox-Gastaut syndrome
Malignant migrating partial seizures of infancy
Paroxysmal extreme pain disorder
Primary erythermalgia
Sodium channelopathy-related small fiber neuropathy
West syndrome
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Romano-Ward syndrome
Autosomal dominant cervical dystonia
Benign essential blepharospasm
Congenital lethal myopathy, Compton-North type
Behavioral variant of frontotemporal dementia
Early-onset autosomal dominant Alzheimer disease
Familial isolated dilated cardiomyopathy
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Leprechaunism
Progressive non-fluent aphasia
Rabson-Mendenhall syndrome
Semantic dementia
Synonym(s):
- GEFS+
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
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
External references:
8 OMIM references -
No MeSH references
No signs/symptoms info available.