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Disease Ontology Browser
autosomal dominant nocturnal frontal lobe epilepsy 3 (DOID:0060684)
Alliance: disease page
Synonyms: ENFL3; nocturnal frontal lobe epilepsy 3
Alt IDs: OMIM:605375
Definition: An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNB2 gene on chromosome 1q21.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory