autosomal dominant nocturnal frontal lobe epilepsy 5 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nocturnal frontal lobe epilepsy 5 (DOID:0060686)
Alliance: disease page
Synonyms: ENFL5; nocturnal frontal lobe epilepsy 5
Alt IDs: OMIM:615005
Definition: An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34.

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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