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Benign familial epilepsy of childhood with rolandic spikes
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant macrothrombocytopenia
3 OMIM references -
4 associated genes
No signs/symptoms info
Benign familial epilepsy of childhood with rolandic spikes
Autosomal dominant macrothrombocytopenia

GRIN2A
(UniProt - OMIM)
 ACTN1
(UniProt - OMIM)
SRPX2
(UniProt - OMIM)
 ITGA2B
(UniProt - OMIM)
ITGB3
(UniProt - OMIM)
TUBB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GRIN2A
(0.62)
ACTN1


Citations in the biomedical literature:


Benign familial epilepsy of childhood with rolandic spikes
GRIN2A SRPX2
Autosomal dominant macrothrombocytopenia
ACTN1 ITGA2B ITGB3 TUBB1



Benign familial epilepsy of childhood with rolandic spikes
Autosomal dominant macrothrombocytopenia

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 hematologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.