ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

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

Rolandic epilepsy - speech dyspraxia

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

Citations in the biomedical literature:

Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation		Rolandic epilepsy - speech dyspraxia

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - 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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.