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Disease Ontology Browser
autosomal dominant nocturnal frontal lobe epilepsy (DOID:0060681)
Alliance: disease page
Synonyms: ENFL
Alt IDs: MESH:C579932, OMIM:PS600513, ORDO:98784
Definition: A frontal lobe epilepsy that is characterized by autosomal dominant inheritance with childhood onset of clusters of brief nocturnal motor seizures with hyperkinetic or tonic manifestations.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/15/2022
MGI 6.22
The Jackson Laboratory