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developmental and epileptic encephalopathy, 13 | RareConnect | RareConnect.io

/undetermined early-onset epileptic encephalopathy

/neonatal-onset developmental and epileptic encephalopathy

/developmental and epileptic encephalopathy, 13

developmental and epileptic encephalopathy, 13

Rare Disease

MONDO:0013801

Also Known As

DEE13EIEE13SCN8A early infantile epileptic encephalopathydevelopmental and epileptic encephalopathy 13early infantile epileptic encephalopathy caused by mutation in SCN8Aearly infantile epileptic encephalopathy-13epileptic encephalopathy, early infantile, 13epileptic encephalopathy, early infantile, type 13SCN8A encephalopathySCN8A epilepsy

Definition

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN8A 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:614558 ↗

GARD

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