About   Help   FAQ
Disease Ontology Browser
autosomal dominant nocturnal frontal lobe epilepsy 1 (DOID:0060682)
Alliance: disease page
Synonyms: ENFL1; nocturnal frontal lobe epilepsy 1
Alt IDs: OMIM:600513
Definition: An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA4 gene on chromosome 20q13.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory