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benign neonatal seizures

Disease Summary
Associated Targets (3)
Tclin

3


Explore Associated Targets
Mondo Description A rare genetic epilepsy syndrome characterized by the occurrence of afebrile seizures in otherwise healthy newborns with onset in the first few days of life.
Disease Ontology Description A neonatal period electroclinical syndrome that is characterized by tonic-clonic seizures in newborns occurring within the first seven days of life and ceasing within the first 15 weeks of life and has_material_basis_in autosomal dominant inheritance of voltage-gated potassium channels or a chromosomal inversion.
Mondo Term and Equivalent IDs
MONDO:0016027:  benign neonatal seizures
NCIT:C117307: 
OMIMPS:121200: 
Orphanet:1949: 
SCTID:38281008: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)