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Disease association ontology term - MONDO:0957248 - developmental and epileptic encephalopathy, 31B

Term summary

ID
MONDO:0957248
Name
developmental and epileptic encephalopathy, 31B
Ontology or CV name
Disease association
Definition
Any developmental and epileptic encephalopathy in which the cause of the disease is a homozygous mutation in the DNM1 gene.

Parents

Annotation

Disease association

MONDO:0957248 - developmental and epileptic encephalopathy, 31B

References:

Genes: