Disease association ontology term - MONDO:0060671 - epilepsy, juvenile myoclonic, susceptibility to, 10

Term summary

ID: MONDO:0060671
Name: epilepsy, juvenile myoclonic, susceptibility to, 10
Ontology or CV name: Disease association

Parents

excluded_subClassOf hereditary disease
is_a inherited disease susceptibility

Annotation

Disease association

MONDO:0060671 - epilepsy, juvenile myoclonic, susceptibility to, 10

References:

PB_REF:0000006

Genes: