Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 31A
rareAny developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.
- Identifiers
- MONDO:0014598 OMIM:616346
- Part of
- DNM1-encephalopathy and neurodevelopmental disorderLennox-Gastaut syndromeNeonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE31A · developmental and epileptic encephalopathy 31A, autosomal dominant · DNM1 early infantile epileptic encephalopathy
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