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Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Landau-Kleffner syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
Landau-Kleffner syndrome

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

COMMON
GENES 		GRIN2A


Citations in the biomedical literature:


Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
GRIN2A
Landau-Kleffner syndrome



Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
Landau-Kleffner syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: any age
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D018887
No signs/symptoms info available.