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Disease association ontology term - MONDO:0100022 - neonatal/infantile epilepsy syndrome

Term summary

ID
MONDO:0100022
Name
neonatal/infantile epilepsy syndrome
Ontology or CV name
Disease association
Definition
An epilepsy sydrome that has an onset during the neonatal or infantile stage of life.

Parents

Annotation

Disease association

MONDO:0013389 - developmental and epileptic encephalopathy, 12

References:

Genes:

MONDO:0012245 - developmental and epileptic encephalopathy, 3

References:

Genes:

MONDO:0014895 - developmental and epileptic encephalopathy, 40

References:

Genes:

MONDO:0018097 - infantile spasms

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Genes: