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developmental and epileptic encephalopathy, 11 | RareConnect | RareConnect.io

/genetic developmental and epileptic encephalopathy

/developmental and epileptic encephalopathy, 11

developmental and epileptic encephalopathy, 11

Rare Disease

MONDO:0013388

Also Known As

DEE11EIEE11SCN2A early infantile epileptic encephalopathydevelopmental and epileptic encephalopathy 11early infantile epileptic encephalopathy caused by mutation in SCN2Aepileptic encephalopathy, early infantile, 11epileptic encephalopathy, early infantile, type 11

Definition

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN2A gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:613721 ↗

GARD

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