Cytoscape Web
Click node...

Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
1 OMIM reference -
1 associated gene
9 connected diseases
No signs/symptoms info
Disease Type of connection
Benign familial epilepsy of childhood with rolandic spikes
Epileptic encephalopathy with continuous spike-and-wave during sleep
Landau-Kleffner syndrome
Rolandic epilepsy - speech dyspraxia
X-linked non-syndromic intellectual deficit
Autosomal dominant nonsyndromic intellectual deficit
Severe intellectual deficit and progressive spastic paraplegia
Autosomal dominant macrothrombocytopenia
X-linked intellectual deficit, Najm type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GRIN2A Q12879138253
No signs/symptoms info available.