developmental and epileptic encephalopathy, 31B

Rare Disease

MONDO:0957248

Also Known As

DNM1-encephalopathy and neurodevelopmental disorderDEE31Bdevelopmental and epileptic encephalopathy 31B, autosomal recessive

Any developmental and epileptic encephalopathy in which the cause of the disease is a homozygous mutation in the DNM1 gene.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

developmental and epileptic encephalopathy, 31A

MONDO:0014598