ODCs

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

PROTEIN INTERACTIONS: 2

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

Dravet syndrome

Intellectual deficiency - hypotonia - spasticity - sleep disorder


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SCN2A SCN1B	(0.83) (0.55)	ANK3 ANK3

Citations in the biomedical literature:

Dravet syndrome		Intellectual deficiency - hypotonia - spasticity - sleep disorder
	Synonym(s): - SMEI - Severe myoclonic epilepsy of infancy		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.