Cytoscape Web
Click node...

Benign familial neonatal-infantile seizures
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intellectual deficiency - hypotonia - spasticity - sleep disorder
1 OMIM reference -
1 associated gene
No signs/symptoms info
Benign familial neonatal-infantile seizures
Intellectual deficiency - hypotonia - spasticity - sleep disorder

KCNQ2
(UniProt - OMIM)
 ANK3
(UniProt - OMIM)
SCN2A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SCN2A
(0.83)
ANK3


Citations in the biomedical literature:


Benign familial neonatal-infantile seizures
KCNQ2 SCN2A
Intellectual deficiency - hypotonia - spasticity - sleep disorder
ANK3



Benign familial neonatal-infantile seizures
Intellectual deficiency - hypotonia - spasticity - sleep disorder

Synonym(s):
- BFNIS
- Benign neonatal-infantile epilepsy
Synonym(s):
(no synonyms)
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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.