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Benign familial neonatal-infantile seizures
1 OMIM reference -
2 associated genes
13 connected diseases
No signs/symptoms info
Disease Type of connection
Benign familial infantile seizures
Early infantile epileptic encephalopathy
Benign familial neonatal seizures
Dravet syndrome
Generalized epilepsy with febrile seizures-plus context
West syndrome
Romano-Ward syndrome
Catecholaminergic polymorphic ventricular tachycardia
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Juvenile myoclonic epilepsy
Familial atrial fibrillation
Familial short QT syndrome
Jervell and Lange-Nielsen syndrome
Synonym(s):
- BFNIS
- Benign neonatal-infantile epilepsy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
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:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KCNQ2 O43526602235
SCN2A Q99250182390
No signs/symptoms info available.