NORD® Rare Disease Database

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Search results for: scn2a

Rare Disease Information from other Sources

This information is shared from trusted third-party resources in partnership with the MONDO Ontology.

seizures, benign familial infantile, 3

Also known as: BFIS3, BFNIS, SCN2A benign familial infantile epilepsy, benign familial infantile convulsions, benign familial infantile epilepsy caused by mutation in SCN2A, benign familial neonatal-infantile seizures, benign neonatal-infantile epilepsy, convulsions benign familial neonatal, convulsions, benign familial infantile, 3, epilepsy, benign neonatal-infantile, seizures, benign familial infantile, 3, seizures, benign familial infantile, type 3, seizures, benign familial neonatal-infantile

developmental and epileptic encephalopathy, 11

Also known as: DEE11, EIEE11, SCN2A early infantile epileptic encephalopathy, developmental and epileptic encephalopathy 11, early infantile epileptic encephalopathy caused by mutation in SCN2A, epileptic encephalopathy, early infantile, 11, epileptic encephalopathy, early infantile, type 11

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