Search Ontology:
Human Disease

autosomal dominant nocturnal frontal lobe epilepsy 3

Term ID
DOID:0060684
Synonyms
  • ENFL3
  • nocturnal frontal lobe epilepsy 3
Definition
An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNB2 gene on chromosome 1q21. https://www.ncbi.nlm.nih.gov/pubmed/11062464
References
Ontology
Human Disease   ( DOID:0060684 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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