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developmental and epileptic encephalopathy, 47 | RareConnect | RareConnect.io

/undetermined early-onset epileptic encephalopathy

/neonatal-onset developmental and epileptic encephalopathy

/developmental and epileptic encephalopathy, 47

developmental and epileptic encephalopathy, 47

Rare Disease

MONDO:0014949

Also Known As

DEE47EIEE47FGF12 early infantile epileptic encephalopathydevelopmental and epileptic encephalopathy 47early infantile epileptic encephalopathy caused by mutation in FGF12epileptic encephalopathy, early infantile, 47epileptic encephalopathy, early infantile, 47; EIEE47epileptic encephalopathy, early infantile, type 47

Definition

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the FGF12 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:617166 ↗

GARD

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