Search Ontology:
Human Disease

autosomal dominant nocturnal frontal lobe epilepsy 5

Term ID
DOID:0060686
Synonyms
  • ENFL5
  • nocturnal frontal lobe epilepsy 5
Definition
An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34. https://www.ncbi.nlm.nih.gov/pubmed/23086396
References
Ontology
Human Disease   ( DOID:0060686 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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