Disease association ontology term - MONDO:0016532 - Lennox-Gastaut syndrome

Term summary

ID

MONDO:0016532

Name

Lennox-Gastaut syndrome

Ontology or CV name

Disease association

Definition

Lennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies.

Parents

• is_a syndromic disease
• is_a genetic developmental and epileptic encephalopathy
• is_a childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy

Annotation