Disease association ontology term - MONDO:0014392 - developmental and epileptic encephalopathy, 25

Term summary

ID

MONDO:0014392

Name

developmental and epileptic encephalopathy, 25

Ontology or CV name

Disease association

Definition

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC13A5 gene.

Parents

• is_a undetermined early-onset epileptic encephalopathy
• is_a neonatal-onset developmental and epileptic encephalopathy

Annotation