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developmental and epileptic encephalopathy, 31A | RareConnect | RareConnect.io

/Lennox-Gastaut syndrome

/undetermined early-onset epileptic encephalopathy

/neonatal-onset developmental and epileptic encephalopathy

/developmental and epileptic encephalopathy, 31A

developmental and epileptic encephalopathy, 31A

Rare Disease

MONDO:0014598

Also Known As

DEE31DNM1-encephalopathy and neurodevelopmental disorderDNM1-related epilepsy and neurodevelopmental disorderEIEE31developmental and epileptic encephalopathy 31early infantile epileptic encephalopathy caused by mutation in DNM1epileptic encephalopathy, early infantile, 31epileptic encephalopathy, early infantile, type 31DEE31ADNM1 early infantile epileptic encephalopathydevelopmental and epileptic encephalopathy 31A, autosomal dominant

Definition

Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 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:616346 ↗

GARD

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