OBO ID: DOID:0060686
Term Name: autosomal dominant nocturnal frontal lobe epilepsy 5 Search Ontology:
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 autosomal dominant nocturnal frontal lobe epilepsy 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KCNT1 Epilepsy nocturnal frontal lobe, 5 615005
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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