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Disease association ontology term - MONDO:0014895 - developmental and epileptic encephalopathy, 40

Term summary

ID
MONDO:0014895
Name
developmental and epileptic encephalopathy, 40
Ontology or CV name
Disease association
Definition
Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GUF1 gene.

Parents

Annotation

Disease association

MONDO:0014895 - developmental and epileptic encephalopathy, 40

References:

Genes: