ODCs

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

COMMON GENES: 1

1 OMIM reference -
6 associated genes
No signs/symptoms info

Female restricted epilepsy with intellectual deficit

Dravet syndrome

Citations in the biomedical literature:

Female restricted epilepsy with intellectual deficit		Dravet syndrome
	Synonym(s): - EFMR - Familial epilepsy and mental retardation limited to females		Synonym(s): - SMEI - Severe myoclonic epilepsy of infancy

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: unknown		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

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

No signs/symptoms info available.