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developmental and epileptic encephalopathy, 41 | RareConnect | RareConnect.io

/undetermined early-onset epileptic encephalopathy

/neonatal-onset developmental and epileptic encephalopathy

/early-infantile DEE

/developmental and epileptic encephalopathy, 41

developmental and epileptic encephalopathy, 41

Rare Disease

MONDO:0014916

Also Known As

DEE41EIEE41SLC1A2 early infantile epileptic encephalopathydevelopmental and epileptic encephalopathy 41developmental and epileptic encephalopathy, 41early infantile epileptic encephalopathy caused by mutation in SLC1A2epileptic encephalopathy, early infantile, 41epileptic encephalopathy, early infantile, 41; EIEE41epileptic encephalopathy, early infantile, type 41

Definition

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC1A2 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:617105 ↗

GARD

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