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

Epileptic encephalopathy with continuous spike-and-wave during sleep

Rolandic epilepsy - speech dyspraxia

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

Citations in the biomedical literature:

Epileptic encephalopathy with continuous spike-and-wave during sleep		Rolandic epilepsy - speech dyspraxia
	Synonym(s): - CSWSS syndrome - ESES - Electrical status epilepticus during slow sleep		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Mental and behavioural disorders -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: any age 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.