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Developmental and epileptic encephalopathy, 31B

MONDO:0957248

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

Also known as: DNM1-encephalopathy and neurodevelopmental disorder, DEE31B, developmental and epileptic encephalopathy 31B, autosomal recessive

17 clinical trials for this condition and its sub-types, 0 tagged with Developmental and epileptic encephalopathy, 31B itself.

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