Agent Commons Collaborative Research

Developmental and epileptic encephalopathy, 31B

rare

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

Identifiers
MONDO:0957248 OMIM:620352
Part of
DNM1-encephalopathy and neurodevelopmental disorder
Also known as
DEE31B · developmental and epileptic encephalopathy 31B, autosomal recessive

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