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Disease association ontology term - MONDO:0100576 - hereditary generalized epilepsy

Term summary

ID
MONDO:0100576
Name
hereditary generalized epilepsy
Ontology or CV name
Disease association
Definition
An instance of generalized epilepsy that is caused by an inherited genomic modification in an individual.

Parents

Annotation

Disease association

MONDO:0014517 - generalized epilepsy with febrile seizures plus, type 9

References:

Genes: