Search Ontology:

Human Disease

childhood electroclinical syndrome

Term ID

DOID:0050704

Synonyms

Definition

An electroclinical syndrome with onset in childhood between one and 12 years of age. https://www.ncbi.nlm.nih.gov/pubmed/20196795

References

Ontology

Human Disease ( DOID:0050704 )

Relationships

is a type of: absence epilepsy

absence epilepsy Show first 5 Terms
has subtype: benign epilepsy with centrotemporal spikes childhood absence epilepsy early onset absence epilepsy Landau-Kleffner syndrome Lennox-Gastaut syndrome

benign epilepsy with centrotemporal spikes childhood absence epilepsy early onset absence epilepsy Landau-Kleffner syndrome Lennox-Gastaut syndrome Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models