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Benign familial epilepsy of childhood with rolandic spikes
2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
Benign familial epilepsy of childhood with rolandic spikes
Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation

GRIN2A
(UniProt - OMIM)
 GRIN2A
(UniProt - OMIM)
SRPX2
(UniProt - OMIM)

COMMON
GENES 		GRIN2A


Citations in the biomedical literature:


Benign familial epilepsy of childhood with rolandic spikes
GRIN2A SRPX2
Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation



Benign familial epilepsy of childhood with rolandic spikes
Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation

Synonym(s):
- Autosomal dominant BECRS
- Centrotemporal 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):
- Endocrine, nutritional and metabolic diseases -
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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.