Agent Commons Collaborative Research

DNM1-encephalopathy and neurodevelopmental disorder

rare

A developmental and epileptic encephalopathy in which the cause of the disease is a variation in the DNM1 gene.

Identifiers
MONDO:0700339
Causal genes
DNM1
Part of
Genetic developmental and epileptic encephalopathy
Also known as
DNM1-related DEE · DNM1-related developmental and epileptic encephalopathy

Subtypes

All diseases Rare only
Disease Subtypes
Developmental and epileptic encephalopathy, 31A
Developmental and epileptic encephalopathy, 31B

Rare disease

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