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Disease association ontology term - MONDO:0014868 - developmental and epileptic encephalopathy, 38

Term summary

ID
MONDO:0014868
Name
developmental and epileptic encephalopathy, 38
Ontology or CV name
Disease association
Definition
Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the ARV1 gene.

Parents

Annotation

Disease association

MONDO:0014868 - developmental and epileptic encephalopathy, 38

References:

Genes: