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Disease association ontology term - MONDO:0700339 - DNM1-encephalopathy and neurodevelopmental disorder

Term summary

ID
MONDO:0700339
Name
DNM1-encephalopathy and neurodevelopmental disorder
Ontology or CV name
Disease association
Definition
A developmental and epileptic encephalopathy in which the cause of the disease is a variation in the DNM1 gene.

Parents

Annotation

Disease association

MONDO:0014598 - developmental and epileptic encephalopathy, 31A

References:

Genes:

MONDO:0957248 - developmental and epileptic encephalopathy, 31B

References:

Genes: